EyePoint Pharmaceuticals Jobs

Be Seen and Heard at EyePoint Pharmaceuticals At EyePoint, leadership trusts our employees to get the job done. The patient-centric and award-winning approach we're taking in business fuels our success for: preventing blindness through vision-saving medications delivering best-in-class proprietary pharmaceutical technologies transforming ocular drug delivery We See You. Your wellbeing Your professional worth Your future at EyePoint EyePoint offers robust total rewards in a science-based entrepreneurial culture that empowers curiosity and innovation to help catapult your career. There's space for every voice and perspective to be heard in our on-site and remote environments where a variety of strengths and diverse backgrounds are connected. Eyepoint Pharmaceuticals is seeking a talented formulator to join our Development group in Watertown MA. Our department works closely with Operations and Regulatory affairs department to formulate and manufacture innovative ocular formulations. Ideal candidate should have a strong background in advanced physical chemistry, the use of polymers in Ocular Delivery. The selected scientist will design and conduct experiments to develop ocular formulations as well as to design and conduct robust analytical experiments for the designed formulations. The qualified candidate will interact with other departments, CMOs, participate in cross functional teams, contribute to the product development plans, and authorship of publications and pertinent sections of regulatory submissions, as needed. Additionally, the candidate must be a strong team player with excellent communication skills working in a complex cross-functional environment. The candidate must be able to work independently and take initiative by providing input on multiple projects. The candidate must be able to think critically, intellectually curious, and show resilience and courage to resolve complex formulation and manufacturing problems. Responsibilities Primary responsibilities include, but are not limited to, the following: Individual responsibilities Develop ocular formulations and manufacturing process for pre-clinical and clinical use. Collaborate with the analytical department and other departments. Generate data for project progression and summarize findings in technical reports. Interpret complicated data sets and provide sound recommendations toward successful development. Present experimental plans and data to project team. Build expertise and knowledge around ocular formulation drug products. Maintain knowledge with up-to-date scientific literature in the field of ocular drug delivery. Qualifications Primary skills and knowledge required include, but are not limited to the following: Understanding of fundamental biopharmaceutical principles for the development of drug products. Hands-on experience with formulation techniques, processing equipment, and unit operations at laboratory scales. Intermediate applied statistical analysis skills. Excellent verbal and written communication skills. Detail-oriented and ability to work on multiple projects concurrently. Preferred Qualifications Experience with solid state analysis, such as Microscopy, DSC, TGA, PXRD. Experience with a range of dosage forms including solid and suspension Ability to effectively and collaboratively participate in technical team discussions. GLP, GMP, and GxP experience is a plus. Level of Education Required: Bachelor degree in pharmaceutics or pharmaceutical sciences Number of Years of Experience in the Function and in the Industry: 1-3 years of industry experience. Envision Your Future With the exciting energy of a winning culture and an exhilarating pace, we are an ophthalmology company committed to preventing blindness by developing and commercializing innovative therapeutics. The collective power of our values influences everything we do, and everything we do for you. Transformational Innovation We exist to change our patients' lives through the power of sight. We are forward looking, embrace challenges with curiosity, and continuously seek to improve our products and ourselves by learning, problem-solving and pushing the limits of science and technology. Unwavering Integrity We recognize our responsibility to our patients, employees, and our community, and value the trust they put in us. We set a high ethical bar and expect responsible leadership at every level to ensure we serve those who matter most to us. Compassionate Excellence We believe that fun and excellence can coexist. We foster a culture where enjoying the work we do and caring for each other are as important as delivering exceptional outcomes. Inclusive Collaboration We strive to see through the eyes of others and work as one team. We appreciate one another's differences and perspectives, and ensure everyone feels valued, respected and encouraged to bring their ideas forward. EyePoint Pharmaceuticals is proud to be an equal opportunity employer. We believe that diversity and inclusion among our colleagues is critical to our success as a company, and we seek to recruit, develop, and retain the most talented people from a diverse candidate pool. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. #LI-Onsite

This role is considered Hybrid. We are seeking a highly organized and experienced Executive Assistant to provide consistent, proactive general administrative and project management support to several leaders within the Medical Affairs leadership team. This role will report to the Head of Medical Affairs and provide support to other Medical Affairs leaders including the VP, Scientific Communications and VP, Global Medical TTR Franchise ensuring efficient management of their schedules, coordination of leadership meetings, and handling various administrative tasks. This individual will be responsible for acting as a professional liaison with internal executives and leaders and high-level external contacts. The successful candidate will have strong Microsoft office skills and will excel in project management, communication and creative problem solving. The successful candidate will be distinguished by their ability to organize work, establish priorities, and meet individual and team goals. It is expected that the Executive Assistant will be a highly effective collaborator and communicator. A successful candidate will have a positive attitude and demonstrate a proven track record of working with executive leadership. Summary of Key Responsibilities * Provides executive administrative support for Medical Affairs leaders including management of complex calendars, assistance with department goals, meetings, calendar, travel, expense reports, etc. * Develops & manages various team collaboration sites and document repositories and distribution lists * Assists with the onboarding of new team members * Acts as a key contact both internally and externally * Manages and prioritizes internal and external communications including emails, arrangement of conference calls and Zoom meetings; prepare formal agendas and other communication/meeting materials for internal and external use. * Coordinate logistics for meetings including leadership team meetings, off-sites, and trainings, including vendor selection, technology setup, etc. * Supports agenda development, meeting minutes, manages files in BOX folders and repositories for large team meetings * Depending on prioritization and bandwidth may provide additional support as needed for the greater department, including travel coordination, cross-functional team calendaring, preparing slide decks for presentations, onboarding of new team members, business supplies & materials, etc. * Participates as integral member of company-wide Executive Admin (EA) team and participates in EA team meetings, initiatives, and coverage * Appropriately manage information of a highly confidential and critical nature * Serves as a subject matter expert for P2P (Procure to Pay) and liaises with FP&A team * Provide back-up support to other assistants as needed * Perform other duties as assigned Qualifications * Bachelor's degree preferred with a minimum of 5 years relevant experience required. * Proven experience as an administrative assistant, secretary, or similar role, preferably within the healthcare or pharmaceutical sector. * Outstanding verbal and written communication skills required with keen attention to accuracy, details, formatting, and grammar. * Expert knowledge of MS Office applications including MS PowerPoint, Excel, Word and Outlook required. * Experience with project management tools and contract management processes is highly desirable. * Additional skills needed for this role include: * High integrity and demonstrated ability to treat confidential information with great discretion * Strong organizational and prioritization skills * A proven, collaborative team player with initiative and enthusiasm for taking on new challenges in a rapidly evolving industry * Ability to execute under tight deadlines with changing priorities * Exercise good judgment and is solution-oriented across a variety of situations in a growing, fast-paced organization. About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by “interfering” with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality. Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as the #1 Large Employer by Boston Globe Top Places to Work in 2023 for the third consecutive year, one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients. Qualified applicants will receive consideration for employment without regard to their race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, ethnicity, marital status, protected veteran status, disability, or any other characteristics prohibited by law.

We are seeking a strategic and collaborative Associate Director of Medical Omnichannel & Digital Engagement to help lead and execute a Global Omnichannel Communication Strategy for therapeutic areas within the Alnylam portfolio. Reporting to the Director of Medical Omnichannel & Digital Engagement, this role is critical in supporting Alnylam's medical digital ecosystem to impact proper channel orchestration of key medical activities. This position is open to remote working and will be primarily located at 675 Kendall, Cambridge, MA while in the office. Key Responsibilities: * Support the development of a Global Omnichannel Communication Strategy for therapeutic areas within the Alnylam portfolio (commercial and pipeline) to impact optimized channel orchestration of key medical activities * Work with multiple stakeholders in a highly matrixed environment, closely interacting with key functional groups such as Digital Marketing, Strategic Technologies, Medical Director Office, Scientific Communications, Field Medical, Legal/Regulatory/Compliance, etc. * Partner with Global and Regional teams across therapeutic areas to advocate for omnichannel capabilities, frameworks, methodologies, and develop use cases to optimize HCP engagement experience * Apply project management expertise to ensure timely and effective implementation of key omnichannel deliverables * Create business case, design, and lead proof of concept/pilots for emerging digital capabilities and enhancements within Alnylam's medical digital ecosystem * Drive the evolution of our medical affairs website, implementing data-driven insights to enhance user experience and engagement * Leverage Veeva Vault to optimize medical communication strategies and digital channel orchestration * Conduct advanced data analysis and insights-driven decision-making to inform digital omnichannel strategy and channel optimization * Implement and manage vendor relationships for digital platforms, maintenance of medical affairs website, and content management systems * Troubleshoot roadblocks and identify creative and compliant solutions to facilitate progress of new initiatives * Stay at the forefront of emerging omnichannel trends, medical digital channel developments, and innovative engagement opportunities within Medical Affairs * Translate analytics results into strategic actionable insights and recommendations for enhancing channel effectiveness and omnichannel campaign performance Qualifications: * Doctorate degree (MD, PharmD, PhD) with a strong scientific background and minimum of 5+ years of relevant work experience * Strong knowledge and hands-on experience of multichannel and/or omnichannel strategy execution * Collaborative mindset with a passion for cross-functional teamwork and an open-minded approach to solving complex challenges * Builds strong relationships to enable higher performance * Demonstrated experience with start-to-finish planning/executing multichannel digital tactics (i.e. CRM programs, websites, email, emerging media tactics, SEO/SEM, social media) * Ability to work on and lead independent initiatives without day-to-day supervision * Strategic thinking with a focus on digital innovation and change management * Commitment to continuous learning and adaptation with a results-oriented mindset * Advanced project management skills with high emotional intelligence and ability to influence and lead (without authority) in matrix organized structure * Experience in working for or with a digital agency is desired/preferred * Technology-savvy with advanced proficiency in data analytics (i.e. PowerBI, GA4, Snowflake) is desired/preferred * Proven expertise in key platforms such as Veeva Vault, Google Analytics (GA4), Web dev is desired/preferred About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by "interfering" with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality. Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as the #1 Large Employer by Boston Globe Top Places to Work in 2023 for the third consecutive year, one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients. Qualified applicants will receive consideration for employment without regard to their race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, ethnicity, marital status, protected veteran status, disability, or any other characteristics prohibited by law.

The Director, Data Management is responsible for the oversight of data management activities in support of Alnylam studies across all stages of clinical drug development. This position reports to the head of the Data Management group. Responsibilities: * Direct and grow internal data management expertise area, including management of direct reports; * Direct and establish standards for data management CRO outsourcing strategy and deliverables, including the CRO selection process and the governance of CRO performance; * Oversee the successful execution of all data management activities in support of Alnylam clinical studies in partnership with CROs, including eCRF development, database build, data collection, data coding, cleaning, database lock and archiving; * Supervise the execution of cross-functional, internal data review plans by direct reports across all Alnylam clinical studies; * Partner with internal and external partners, including Biostatistics, Statistical Programming, Clinical Operations, Clinical Research, Quality Assurance, Clinical Pharmacology and Pharmacometrics, Bioanalytical, Global Patient Safety & Risk Management (GPSRM), Regulatory Affairs, and Medical Affairs; CROs, central and local laboratories, and other vendors; * Lead development and implementation of data collection standards, consistent with industry best practice; * Lead data management contributions to the development of clinical protocols, clinical study reports and other regulatory documents, e.g. DSURs, Briefing Documents, etc. * Oversee development of department workflows, and infrastructure strategy and implementation, such as preferred provider initiatives, SOPs, and templates; * Collaborate with Statistical Programming and external vendors to ensure compliance of SDTM clinical datasets, consistent with CDISC standards; * Collaborate with Clinical Operations and Quality Assurance to certify the integrity and traceability of all clinical data sources, compliant with 21 CFR Part 11 standards; * Direct Data Management GCP inspection readiness efforts; function as a leader for Data Management in GCP inspections; * Represent Data Management at internal cross-functional meetings and external vendor leadership meetings; * Demonstrate clear alignment with Alnylam Core Values including, Commitment to People, Fiercely Innovative, Purposeful Urgency, Open Culture and Passion for Excellence. Requirements * BS/BA in scientific discipline, MS or equivalent preferred, with at least 15 years of clinical data management experience in a pharmaceutical/biologics/biotechnology company, with at least 5 years in a leadership capacity; * Extensive experience managing global studies utilizing an outsourced CDM model from start-up through close-out; * Extensive experience managing direct reports and providing performance reviews and career development guidance; * Understanding of ICH GCP as well as general knowledge of industry practices and standards; * Knowledge and understanding of regulatory requirements and expectations for clinical data systems including 21 CFR Part 11; * Expert knowledge of eClinical processes, efficient design/build of an EDC data management system and other Clinical Trial data/Data Management Systems; * Expert knowledge and understanding of regulations and industry-adopted data standards, such as CDISC-SDTM and CDASH; * Experience using standardized medical terminology, including MedDRA and WHODrug; * Experience working Medidata Rave EDC systems; * Experience working with MS Office Suite (Excel, Word and PowerPoint) familiar with MS Project; * Excellent written and oral communication skills; * Highly motivated and flexible, with excellent organizational skills; * Ability to work independently and as part of a multi-disciplinary team. About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by "interfering" with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality. Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as the #1 Large Employer by Boston Globe Top Places to Work in 2023 for the third consecutive year, one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients. Qualified applicants will receive consideration for employment without regard to their race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, ethnicity, marital status, protected veteran status, disability, or any other characteristics prohibited by law.

The Principal Medical Writer represents medical writing on multi-disciplinary teams, collaborates on the development of clinical documents in accordance with all applicable regulations, Good Clinical Practices, and Standard Operating Procedures (SOPs), and oversees the work of internal and contract writers. This is an individual contributor position, equivalent to the Associate Director, without direct report responsibilities. Responsibilities: * Produce high-quality and on-time clinical documents * Independently plan, coordinate, develop, update, and revise key documents, including clinical protocols, investigator brochures, clinical study reports, integrated efficacy and safety summaries, and related documents. * Independently lead supplemental filings, Type 2 Variations, rest-of-world filings, and clinical responses to questions * Provide medical writing subject matter expertise and leadership to project teams and collaborate with the Medical Writing line management to ensure proper planning and resourcing for upcoming project team writing deliverables. * Facilitate/manage efficient review and finalization process for documents produced internally and/or externally by consultants, contractors and vendors. * Collaborate effectively with Biometrics, Clinical Operations, Clinical Development, Pre-Clinical Development, Program Management, Research, Quality, and Corporate Communications, Medical Affairs, as well as with external stakeholders. * Contribute to the development and standardization of templates and related processes to support the medical writing needs of a growing organization and assist in training staff and contractors on MW processes. * Provide medical writing subject matter expertise and oversight for post-approval regulatory documents, such as PASS and other non-interventional protocols. * Assist the line managers in the training and development of junior staff. Qualifications: * Bachelor's degree in Life Science with relevant writing expertise or in English/Communications with relevant science expertise. Advanced degree and/or professional certification/credentials preferred. * 7+ years of experience as a medical writer in the sponsor/CRO setting. Experience with regulatory submissions (NDA/BLA/MAA) strongly preferred. CTA/IND experience is a plus. * Some experience with developing MW processes and standards preferred * In-depth knowledge of Good Clinical Practices, FDA regulations, ICH guidelines, and the drug development process. * Successful track record of managing multiple projects in a fast-paced and deadline-driven environment. * Knowledge of eCTD formatting and EDMS systems preferred. * Experience overseeing the work of contract writers. * Impeccable attention to detail. * Must be proficient with Microsoft Windows, Word, Excel, and PowerPoint. * Demonstrate clear alignment with Alnylam Core Values including, * Commitment to People * Innovation and Discovery * Purposeful Urgency * Open Culture * Passion for Excellence. About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by "interfering" with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality. Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as the #1 Large Employer by Boston Globe Top Places to Work in 2023 for the third consecutive year, one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients. Qualified applicants will receive consideration for employment without regard to their race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, ethnicity, marital status, protected veteran status, disability, or any other characteristics prohibited by law.

Be Seen and Heard at EyePoint Pharmaceuticals At EyePoint, leadership trusts our employees to get the job done. The patient-centric and award-winning approach we're taking in business fuels our success for: preventing blindness through vision-saving medications delivering best-in-class proprietary pharmaceutical technologies transforming ocular drug delivery We See You. Your wellbeing Your professional worth Your future at EyePoint EyePoint offers robust total rewards in a science-based entrepreneurial culture that empowers curiosity and innovation to help catapult your career. There's space for every voice and perspective to be heard in our on-site and remote environments where a variety of strengths and diverse backgrounds are connected. This person will report directly to the Quality Control Manager and will be responsible for all aspects of quality control in respect to clinical trial materials and commercial products as required. This position provides production support for incoming, in process production and final product test and inspection. The individual will work in the GMP Incoming Quality room to ensure that all Raw Materials are tested, as well as all Final Product testing that is performed by CTOs. That all test results are approved for release in accordance to all applicable GMP regulations and guidelines (e.g. 21CFR Parts 11, 210/211, 820, (USP/EP/JP), ICH Guidelines), as well as company's procedures. This position is located at our Northbridge, MA site. Responsibilities Primary responsibilities include, but are not limited to, the following: Individual responsibilities Primary responsibilities include, but are not limited to, the following: Perform sample management and inspection quality assurance (IQA) of raw materials, components, in-process production and final product, as required. Maintain inspection data trend charts as well as chart recorder records. Adhere to the GMP Quality Management System (QMS) to ensure compliance with documented policies, procedures and work instructions. Identify IQA anomalies and/or discrepancies then escalate to QC Manager in a timely manner Provide support for investigations regarding deviations, out-of-trend (OOT)/out-of-specification (OOS) results, Material Evaluation Reports or Environmental Alert/Action Report (EAR). Use SOPs, WIs, Specifications, Trends, other applicable references and expertise to propose solution(s) to QC inspection issues. Provide QC inspection support for protocols and reports as appropriate. Plan and perform workload to meet schedules, timelines, deadlines as per procedure's and/or department requirements. Participate in group and/or project teamwork for project and process improvements. Support internal and external audits and regulatory inspections, as required. Identify gaps in systems and procedures. Review proposed changes to systems, procedures, methods, as appropriate. Quality assurance activities as required including but not limited to line clearance and production inspection. Participate as Subject Matter Expert (SME) during Regulatory Inspections, as appropriate. Perform visual and dimensional inspections of raw materials utilizing equipment such as microscopes, calipers, micrometers. Qualifications Primary skills and knowledge required include, but are not limited to the following: Previous GMP experience or other regulated industry is required. Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently. Self-starting motivated person who possesses good interpersonal skills and who is able to effectively interact with all departments with the Company. Must have good organizational and verbal communication skills. Adept at using Microsoft Office Products. Must be a team player with integrity and concern for the quality of Company products, services and staff members. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Ability to lift up to 50 lbs. on occasion. Ability to work on your feet in a classified clean room environment for up to 5 hours per day Level of Education Required: Technical High School Diploma Preferred Field of Study: ASQ Certified Quality Technician (CQT) certification is a plus Number of Years of Experience in the Function and in the Industry: Two years of GMP or other regulated industry experience Envision Your Future With the exciting energy of a winning culture and an exhilarating pace, we are an ophthalmology company committed to preventing blindness by developing and commercializing innovative therapeutics. The collective power of our values influences everything we do, and everything we do for you. Transformational Innovation We exist to change our patients' lives through the power of sight. We are forward looking, embrace challenges with curiosity, and continuously seek to improve our products and ourselves by learning, problem-solving and pushing the limits of science and technology. Unwavering Integrity We recognize our responsibility to our patients, employees, and our community, and value the trust they put in us. We set a high ethical bar and expect responsible leadership at every level to ensure we serve those who matter most to us. Compassionate Excellence We believe that fun and excellence can coexist. We foster a culture where enjoying the work we do and caring for each other are as important as delivering exceptional outcomes. Inclusive Collaboration We strive to see through the eyes of others and work as one team. We appreciate one another's differences and perspectives, and ensure everyone feels valued, respected and encouraged to bring their ideas forward. EyePoint Pharmaceuticals is proud to be an equal opportunity employer. We believe that diversity and inclusion among our colleagues is critical to our success as a company, and we seek to recruit, develop, and retain the most talented people from a diverse candidate pool. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. #LI-Onsite

The Senior Facilities Technician will support Facilities operations at the Kendall Square Campus. This role is responsible for the repair and maintenance of a wide range of Laboratory equipment, building, and utility systems. Responsibilities include execution of corrective and preventive maintenance, operation/monitoring of building systems, equipment, and programs in a safe and compliant manner. This position will ensure sustained operation of the process and utility systems with minimal interruptions. The Senior Facilities Technician supports the facilities team and contractors to ensure timely on-schedule completion of corrective / preventive maintenance. All duties are performed with the intent to ensure operational capabilities are sustained with emphasis on quality of work and customer service. The Senior Facilities Technician will independently support Facilities management in the day-to-day operations of their assigned areas and report all issues in a timely manner. This position is onsite and will be primarily located at our Kendall Campus in Cambridge MA. Key Responsibilities * Support of operations including the operation and maintenance of utility systems, solvent delivery, support, and process equipment. * Responsible for alarm response and remediation as well as trouble call triage * Develop and maintain standard operating procedures, preventive maintenance plans, spare parts inventories. * Start-up/shutdown and operations of the various equipment and systems within the Kendall site Facility's. * To guide and ensure a safe work environment is maintained through adherence to EH&S and Facilities guidelines and policies. * Support installation, repair, and troubleshooting for a wide range of equipment and instrumentation used for all functions at the Kendall Labs. * Perform scheduled, corrective, and emergency maintenance on process and lab support equipment. * Responsible for the operational readiness of the equipment, working closely with peers ensuring deficiencies are resolved and with completeness. * Capable of full participation in an onsite Chemical Spill Emergency Response team including being able to utilize respiratory protection and being able to successfully complete required medical clearances to utilize personal protective equipment while performing strenuous activities Qualifications * High school diploma with a minimum of 6-10 years of related experience. * Ability to work third shift hours. * Extensive knowledge of building utility systems. * Previous experience in a cGMP environment is a plus. * Experience documenting work in a CMMS preferable. * Must have excellent interpersonal and customer service skills. * Wastewater treatment license (or ability to obtain). * General mechanical skills with a variety of hand tools, meters, ect. * Capable of working in environments requiring use of increased personal protective equipment including chemical containment suits and respiratory protection. * Capable of lifting/lowering, pushing/pulling, and carrying equipment of different dimensions and weights and utilizing equipment to assist in material handling activities.

This role is considered Hybrid. We are seeking an effective Procurement Operations Senior Analyst to join our team. Reporting to the Associate Director, Procurement Operations, the role is responsible for the efficient and effective management of day-to-day purchasing activities within their assigned Expertise Area (EA) - Tech Ops & Quality (TOQ). This role is crucial to ensuring compliance with procurement policies, optimizing spend, and delivering exceptional customer service. This Senior Analyst will collaborate closely with cross-functional teams across the organization and will specialize in managing goods and services purchases in the IT, Facilities, and Tech Ops & Quality areas of Alnylam. This role is a hybrid role with 2 days a week in our Kendall Square office. Key Responsibilities * Procurement Execution: Manage and process purchase requisitions, ensuring adherence to cost-efficiency and quality standards. Identify and resolve bottlenecks to optimize requisition workflow. * Expertise and Guidance: Serve as the Subject Matter Expert (SME) for Ariba within the EA, providing guidance to stakeholders on the Source-to-Pay (S2P) process. Offer training and support to colleagues to enhance procurement knowledge. * Stakeholder Management: Build strong relationships with EA stakeholders to understand their needs, identify purchasing trends, and implement process improvements. Regularly engage with stakeholders to ensure satisfaction and gather feedback. * Process Improvement: Analyze procurement processes to identify opportunities for optimization. Collaborate with cross-functional teams to implement process enhancements that improve efficiency, reduce costs, and enhance customer satisfaction. * Data Analysis: Conduct spend, supplier, and market analysis to identify cost-saving opportunities and inform procurement strategies, new buying channels or catalogs. * Supplier Issue Management: When needed, manage supplier relationships, resolve issues, and ensure timely resolution of invoice discrepancies. * Sourcing: Drive teams to the use of preferred suppliers and lead small-scale sourcing events using SAP Ariba's Collaboration Requisitioning feature as needed. Qualifications * Bachelor's degree required. BS in a technical discipline, such as accounting or finance, desired * 3-5 years general business such as accounting and finance; procurement, supply chain, and/or purchasing experience, a plus * Pharmaceutical industry knowledge, a plus * Experience working with IT, Facilities, Tech Ops & Quality goods and services, a plus * Proficiency in Source-to-Pay systems including Workday Sourcing, Ironclad, Lextegrity, Process Unity, Ariba Guided Buying, VIM, SAP S4 Hana, and Ariba SLP * Excellent analytical and problem-solving skills. * Strong attention to detail and organizational abilities. * Ability to build and maintain strong relationships with stakeholders. * Demonstrates effective interpersonal skills, written and verbal communication skills in stakeholder interactions to ensure exceptional service and consistent interactions. * Must be highly motivated and comfortable working both independently and in a team environment. * Proven ability to contribute in a fast-paced environment with the ability to prioritize tasks and handle time efficiently About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by "interfering" with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality. Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as the #1 Large Employer by Boston Globe Top Places to Work in 2023 for the third consecutive year, one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients. Qualified applicants will receive consideration for employment without regard to their race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, ethnicity, marital status, protected veteran status, disability, or any other characteristics prohibited by law.

We are seeking a Senior Internal Auditor to be a key contributing member of the Internal Audit function for one of Cambridge's most innovative, publicly traded biotech companies. Reporting to the Internal Audit Senior Manager, the ideal candidate will have a solid background in audit, strong communications skills, the ability to collaborate with team members and stakeholders, and an enthusiastic drive to enhance risk management and internal control through thoughtful and robust assurance activities. This is an excellent opportunity to expand your skills and experience as a member of a dynamic team at a company with a great culture and a deep appreciation of the value of an effective Internal Audit function. This position is hybrid onsite and remote working and will be primarily located at Alnylam's Cambridge, MA office. Key Responsibilities * Support the execution of financial, compliance, and operational internal audits, both domestic and abroad to assess Alnylam's risk management and internal control environment. * Under the direction of the auditor in charge, perform audit procedures, including planning, scoping, and fieldwork execution in line with quality standards and timelines. * Assist with certain aspects of Alnylam's SOX program, coordinating with our co-sourced partner who is responsible for SOX controls testing. * Apply a systematic and risk-focused approach to evaluate and improve the effectiveness and efficiency of processes, internal controls, risk management and governance processes. * Leverage analytics and data-driven audit techniques in the execution of audit activities. * Prepare insightful written audit observations and work collaboratively with other expertise areas and the business to align audit findings and management action plans. * Build strong relationships with key stakeholders across the organization while promoting ethical awareness. * Maintain the highest standards of professionalism and independence in the execution of responsibilities. * Support the operation and evolution of the Internal Audit function to keep pace with Alnylam's growth and priorities. Qualifications * Bachelor's degree in accounting, finance, or related field * CPA, CIA, or equivalent professional certification is required * A minimum of 3 years' relevant experience in audit and controls functions * Experience with auditing and advising on governance, risk and controls including a strong understanding of audit principles and methodology * Experience with SAP ERP, audit software, AI, and data visualization or analytic technology preferred * Excellent project management skills with the ability to coordinate and manage multiple priorities * Willing to travel up to 15%, domestic and international About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by "interfering" with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality. Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as the #1 Large Employer by Boston Globe Top Places to Work in 2023 for the third consecutive year, one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients. Qualified applicants will receive consideration for employment without regard to their race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, ethnicity, marital status, protected veteran status, disability, or any other characteristics prohibited by law.

This role is considered Hybrid. This position develops, implements, and oversees processes and procedures for clinical trial ICSR processing activities, including oversight of the case processing outsourced service provider(s). The incumbent will work in close collaboration with pharmacovigilance physicians and cross-functional team members on operational safety issues. This individual will ensure that vendors are following relevant safety management plans and providing high quality ICSRs, through collection and analysis of KPIs. This individual will ensure compliance and adherence to Alnylam pharmacovigilance processes and global regulatory requirements. Summary of Key Responsibilities * Provide pharmacovigilance operations leadership and guidance to cross-functional teams for Alnylam's clinical development programs, serving as the subject matter expert on regulations and best practices for handling safety data in Alnylam's global safety database. * Responsible for development and maintenance of Safety Management Plans for Alnylam clinical trials * Provide expert safety input and review of study specific documents (e.g., protocols, IBs, Pharmacy Manuals) * Collaborate with Global Safety Systems team to support configuration of study specific requirements and reporting rules. * Proactively identify process gaps and implement mitigations to ensure compliance with GCP and GVP regulations and study-specific protocols. * Provide direction and leadership for clinical trial case processing activities to outsourced service provider(s) * Develop Clinical Trial PV training materials to support new and existing projects. * Develop and refine controlled documents and tools, in collaboration with cross functional teams, CROs and vendors to execute best pharmacovigilance practices and maintain regulatory compliance. * Works with the Quality organization for audit and inspection preparedness and supports GPSRM during regulatory inspections and audits. * Oversees completion of SAE reconciliation activities end end-of-study unblinding, in accordance with study timelines. * Assist in conducting training to new team members and less experienced Global Safety Operations team members. * Act as Global Safety Operations functional representative on cross functional projects Qualifications Alnylam prides itself on its entrepreneurial, fast-paced environment where success is rapidly rewarded. There is a strong pipeline, significant resources, and every intention of continuing the phenomenal rate of success and growth. This position offers an opportunity to have tremendous impact on the growth of the company. The culture values hard-work, creativity, flexibility, a sense of humor and a hands-on, problem-solving attitude. The ideal candidate will have the following mix of personal and professional characteristics: * University degree in biological or natural science or health care discipline required. * Minimum of eight years relevant experience in Patient Safety activities in pharmaceutical industry * Demonstrated ability to understand, interpret, analyze, and clearly present scientific and medical data in verbal and written format. * Solid understanding of systems and reporting tools utilized to support pharmacovigilance activities. * Demonstrated ability to be highly collaborative and effective in a team environment (including Safety, Clinical Development, Medical Affairs, Clinical Operations, Biostatistics and Regulatory), as well as with external colleagues for partnered products. * Demonstrated ability to lead and mentor personnel. * Ability to work independently, with minimal supervision. * Excellent written and verbal communication skills * Solid experience in drug development process * Solid understanding of applicable global clinical trial safety regulations and post marketing regulations and experience in participation in regulatory inspections/audits * Strong organizational skills * Experience with overseeing and coordinating work with external vendors. * Ability to comply with Global regulatory requirements (i.e., ICH, GVP, FDA, MHRA, EMA) About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by “interfering” with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality. Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients.

Formulate Your Future Internship at EyePoint June 2 - August 8, 2025 Watertown, MA Be Seen and Heard at EyePoint Pharmaceuticals At EyePoint, leadership trusts our employees to get the job done. The patient-centric and award-winning approach we're taking in business fuels our success for: preventing blindness through vision-saving medications delivering best-in-class proprietary pharmaceutical technologies transforming ocular drug delivery We See You. Your wellbeing Your professional worth Your future at EyePoint EyePoint offers a science-based entrepreneurial culture that empowers curiosity and innovation to help catapult your career. There's space for every voice and perspective to be heard in our on-site and remote environments where a variety of strengths and diverse backgrounds are connected. Formulate Your Future at EyePoint! Are you ready to turn your passion into experience? At EyePoint, we believe internships aren't just about coffee runs-they're about real-world impact, hands-on learning, and meaningful projects that set you up for success. As an EyePoint Intern, you will: • Dive into real projects that directly impact our business goals. • Collaborate with cross-functional teams to solve exciting challenges. • Attend community service events, and mentorship sessions. • Present your contributions to leadership at the end of your internship. The Summer Intern will report directly to the VP, Clinical Development and will be responsible for assisting with compiling the data from the EyePoint clinical studies. This position is located at our Watertown, MA site. We offer a hybrid work schedule. Responsibilities Primary responsibilities and projects to be completed include the following: This individual will assist the clinical development team and, in collaboration with cross-functional team, will help review and compile data from the clinical studies. This will include generating summary report and/or PowerPoint presentations. Qualifications Primary skills and knowledge required include, but are not limited to the following: Able to review, interpretate data and summarize in a concise fashion. Critical and logical thinking is necessary for this position Level of Education Required: Must be a student in a Bachelor's degree program at an accredited college/university Undergraduate student with a minimum of Rising status. Preferred Field(s) of Study: Science major, pre-Med track prefer Envision Your Future With the exciting energy of a winning culture and an exhilarating pace, we are an ophthalmology company committed to preventing blindness by developing and commercializing innovative therapeutics. The collective power of our values influences everything we do, and everything we do for you. Transformational Innovation We exist to change our patients' lives through the power of sight. We are forward looking, embrace challenges with curiosity, and continuously seek to improve our products and ourselves by learning, problem-solving and pushing the limits of science and technology. Unwavering Integrity We recognize our responsibility to our patients, employees, and our community, and value the trust they put in us. We set a high ethical bar and expect responsible leadership at every level to ensure we serve those who matter most to us. Compassionate Excellence We believe that fun and excellence can coexist. We foster a culture where enjoying the work we do and caring for each other are as important as delivering exceptional outcomes. Inclusive Collaboration We strive to see through the eyes of others and work as one team. We appreciate one another's differences and perspectives, and ensure everyone feels valued, respected and encouraged to bring their ideas forward. EyePoint Pharmaceuticals is proud to be an equal opportunity employer. We believe that diversity and inclusion among our colleagues is critical to our success as a company, and we seek to recruit, develop, and retain the most talented people from a diverse candidate pool. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. #LI-Hybrid

This role is considered On-Site. Join our innovative research and development (ReDev) team, dedicated to advancing oligonucleotide-based therapeutics. We are seeking a highly skilled Ph.D. scientist with expertise in drug disposition mechanisms and pharmacokinetic/pharmacodynamic (PK/PD) relationships. As a key representative of the DMPK function, you will collaborate with cross-functional teams to propel novel therapeutics into clinical development. Key Responsibilities * Design and execute in vitro and in vivo drug metabolism, disposition, and pharmacokinetics studies to characterize and optimize the pharmacokinetic and metabolic properties of oligonucleotide-based therapuetic candidates. * Apply quantitative analysis and mathematical modeling to integrate literature and competitor data on pharmacokinetics, pharmacodynamics, pharmacology, safety, and efficacy. Use this integrated data to evaluate and optimize the developability of therapeutic candidates. * Draft and review PK, PK/PD, and toxicokinetic (TK) study reports, as well as nonclinical sections of Investigational Brochure (IB), to support regulatory submission for early clinical development. * Represent the DMPK function on interdisciplinary project teams, collaborating with Research, Toxicology, Bioanalysis, and Clinical Pharmacology groups to ensure high-quality, data-driven nonclinical-to-clinical translation and contribute to shaping clinical development strategies. Qualifications * Educational Background: Ph.D. in Pharmacokinetics, Pharmacology, Biophysics, Bioengineering, or a related field. * Expertise: 0-2 years of experience in the biotech or pharmaceutical industry, with a strong understanding of PK and PK/PD principles. Proficiency in model-based data integration, analysis, and projection. * Passion for Drug Discovery: Demonstrated innovative and critical thinking skills in disease mechanisms and drug discovery processes, with a proven ability to solve complex problems through hypothesis-driven study design and investigation. * Communication and Teamwork: Strong interpersonal, written, and verbal communication skills, with a demonstrated ability to collaborate effectively in a team environment. About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by “interfering” with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality. Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients.

Formulate Your Future Internship at EyePoint June 2 - August 8, 2025 Watertown, MA Be Seen and Heard at EyePoint Pharmaceuticals At EyePoint, leadership trusts our employees to get the job done. The patient-centric and award-winning approach we're taking in business fuels our success for: preventing blindness through vision-saving medications delivering best-in-class proprietary pharmaceutical technologies transforming ocular drug delivery We See You. Your wellbeing Your professional worth Your future at EyePoint EyePoint offers a science-based entrepreneurial culture that empowers curiosity and innovation to help catapult your career. There's space for every voice and perspective to be heard in our on-site and remote environments where a variety of strengths and diverse backgrounds are connected. Formulate Your Future at EyePoint! Are you ready to turn your passion into experience? At EyePoint, we believe internships aren't just about coffee runs-they're about real-world impact, hands-on learning, and meaningful projects that set you up for success. As an EyePoint Intern, you will: • Dive into real projects that directly impact our business goals. • Collaborate with cross-functional teams to solve exciting challenges. • Attend community service events, and mentorship sessions. • Present your contributions to leadership at the end of your internship. Responsibilities The Summer Intern will report directly to the Analytical Scientist I and will be responsible for assisting with in-vitro release testing of drug products. Primary responsibilities and projects to be completed include the following: Responsible for analytical characterization to support Research and Product Development efforts. Key areas of responsibility Performing analytical characterization of development drug products Tabulating and analyzing results of characterization experiments Qualifications Primary skills and knowledge required include, but are not limited to the following: Major in Chemistry, Materials Science or related discipline Laboratory research experience (particularly analytical sciences) is a plus (academic or industry) Previous experience with HPLC is a plus Good computer skills Excellent communication skills Ability to work in a dynamic, small drug company. Personal Qualities: Bright, energetic, hard-working, and creative. Level of Education Required: Must be a student in a Bachelor's degree program at an accredited college/university Undergraduate student with a minimum of Rising status. Preferred Field(s) of Study: Chemistry or Material Science Envision Your Future With the exciting energy of a winning culture and an exhilarating pace, we are an ophthalmology company committed to preventing blindness by developing and commercializing innovative therapeutics. The collective power of our values influences everything we do, and everything we do for you. Transformational Innovation We exist to change our patients' lives through the power of sight. We are forward looking, embrace challenges with curiosity, and continuously seek to improve our products and ourselves by learning, problem-solving and pushing the limits of science and technology. Unwavering Integrity We recognize our responsibility to our patients, employees, and our community, and value the trust they put in us. We set a high ethical bar and expect responsible leadership at every level to ensure we serve those who matter most to us. Compassionate Excellence We believe that fun and excellence can coexist. We foster a culture where enjoying the work we do and caring for each other are as important as delivering exceptional outcomes. Inclusive Collaboration We strive to see through the eyes of others and work as one team. We appreciate one another's differences and perspectives, and ensure everyone feels valued, respected and encouraged to bring their ideas forward. EyePoint Pharmaceuticals is proud to be an equal opportunity employer. We believe that diversity and inclusion among our colleagues is critical to our success as a company, and we seek to recruit, develop, and retain the most talented people from a diverse candidate pool. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. #LI-Onsite

The Director, Statistical Programming provides statistical programming leadership and guidance for early/late phase studies across a compound and/or complex clinical development program(s). He/she is responsible for overseeing all statistical programming activities across a compound, including technical and project leadership overseeing the quality and timely delivery of all statistical programming deliverables for studies and/or for worldwide regulatory submissions. He/she ensures the team develops, maintains, validates and runs quality SAS programs that access, visualize, analyze, and report clinical trial data in accordance with statistical analysis plans, ICH guidelines, and applicable regulatory requirements. He/she leads process, technology or standard initiatives that add efficiencies and capabilities to the Statistical Programming and/or Data Sciences, Statistics, and Epidemiology (DSSE) department. He/she directs and partners with Statistical Programming vendors to support all programming activities and priorities. Summary of Key Responsibilities * Leads statistical programming teams/activities for complex clinical development Compound(s), including worldwide regulatory submissions. Represents Statistical Programming as part of Clinical Trial Working Groups (CTWG), Clinical Development Teams, and/or Clinical Filing teams, and acts as a key decision-maker with biostatistics and data management on DSSE' analysis/dataset and electronic submission strategies; * Plans optimal programming and data/analysis review tasks and team member assignments, coordinates and leads programming team delivery/forums; Revisits and aligns staffing plans and programming assignments seamlessly as priorities shift; * Drives analysis dataset/submission flow with Biostatistics, working closely on the development and review/validation of Statistical plans/shells, CDISC SDTM and ADaM specifications and datasets, TLFs and electronic submissions; * Drives clinical data review and validation flow with Data Management including the development and review of DM documentation (i.e., Data Review Plans, Data Transfer Agreements, etc.), CDISC SDTM specifications, datasets, P21 reporting, and SDTM Reviewer Guides and define packages; * Coordinates delivery of PV outputs to Drug Safety to support timely Safety review * Partners with Clinical Pharmacology to coordinate PK/PD Analyses delivery for Clinical Study Reports, clinical dataset provisioning and other compound data delivery or analytic/modeling needs, as needed; * Directs internal and external statistical programmers and vendors to deliver high-quality and timely delivery; maintains strong collaboration and partnership with preferred vendors through two-way communication, prioritization, collaboration, proactive issue detection and remediation; * Leads team to complete complex SAS tasks, including development of SDTM production/validation, ADaM datasets/specifications production/validation, TLF delivery, Defines, reviewer guides, other programming tasks as requested or TLF annotations for multiple studies and/or across an integrated summary/compound; * Mentor's statistical programmers working on the program; Promotes productive work environment through teamwork, quality, innovation and leadership of Programming and DSSE forums. Ensures team compliance with SOPs and departmental standards; * Leads process, macro/tool or standards initiatives or sub teams to achieve programming efficiency and/or programming effectiveness; Brings forward industry best practices to DSS processes, systems, or standards. Authors SOPs/best practices and rolls out training/methods; * Exercises leadership within SP Department, as well as the broader DSSE Expertise Area; * Communicates and influences effectively across various levels and relevant functions, CTWG, Filing teams and/or senior stakeholders, on relevant Project or SP topics; * Supervises, coaches and develop statistical programmers in their day to day tasks and supports their career development and learning, Qualifications Typically demonstrates the following, or equivalent, qualifications: * At least 12 years' industry (Pharmaceutical, Biotech, CRO) SAS programming experience or equivalent; * At least 3 years as a people manager, including authorship of performance evaluations * Significant experience leading programming teams in support of clinical development compounds to report the results of clinical trials, integrate analyses across a program, and prepare data/analysis for electronic NDA or BLA submission; * Expert at the creation of technical programming specifications, standards and producing complex, validated SAS programs; * Demonstrated experience in leading teams to implement submission-ready CDISC standards, including SDTM, and ADaM, Data Reviewer guides, and Define xml for multiple studies across a compound and for regulatory submission; * Excellent collaboration and partnership skills with cross-functional peers in Clinical Operations, Regulatory, Medical Writing, Safety, Clinicians, Medical Affairs, etc. and/or vendor relationships; * Expert knowledge of SAS/Base, SAS/Macro, SAS/STAT, SAS/Graph, and SAS/SQL with a demonstrated mastery of SAS/STAT procedures; * Experience independently developing processes/SOPs, Standards or implementing programming best practices; * Experience leading and maintaining positive vendor relationships in support of a compound/program in the delivery of quality programming support; * Excellent written and oral communication, planning and organizational skills required; * Expert problem-solving and decision-making skills with respect to best practices for Programming, and compound, data or submission strategies * Experience leading statistical programming process or technology improvement projects through to implementation * Bachelor's Degree required, Master's Degree Preferred, in areas of computer science, statistics, mathematics or information sciences. * Clear alignment with Alnylam Core Values: * Commitment to People * Innovation and Discovery * Sense of Urgency * Open Culture * Passion for Excellence About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by "interfering" with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality. Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as the #1 Large Employer by Boston Globe Top Places to Work in 2023 for the third consecutive year, one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients. Qualified applicants will receive consideration for employment without regard to their race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, ethnicity, marital status, protected veteran status, disability, or any other characteristics prohibited by law.

The Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data. Summary of Key Responsibilities * Represents biostatistics at cross-functional team meetings to drive clinical development of drug candidate and provides input on clinical development plans. * Collaborates with Clinical Development, Regulatory and Clinical Operations Expertise Areas to design clinical trials. * Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts. * Contributes to or prepares statistical analysis plans. * Collaborates with Data Management, Clinical Development and Clinical Operations on design of eCRFs. * Provides statistical guidance on conduct of ongoing trials. * Collaborates with Statistical Programmers on summary and analysis of trial data. * Writes ADS and ad hoc analysis specifications. * Contributes to clinical study reports and other regulatory documents e.g. DSURs, Briefing Documents, etc. * Represents Alnylam in meetings with regulators, Key Opinion Leaders, partners, and * other stakeholders * Contributes to scientific articles, summarizing data collected in Alnylam trials. * Participates in other activities and meetings to support Biostatistics and the * Development Team as needed. * Consults with Research & Preclinical colleagues on statistical questions in their work. * Manages CRO statistical and programming support. Qualifications * Ph.D. in Biostatistics or Statistics or Equivalent with at least 7 years pharmaceutical biostatistics experience; or MS with at least 10 years relevant experience. * Excellent written and oral communication and presentation skills. * Experience programming in SAS. * Interest in and basic understanding of biology and biological processes, including RNAi. Desired Experience: * Experience in clinical development through Phase 3 (NDA submission). * Experience as lead statistician for a compound * Understanding of ICH GCP as well as general knowledge of industry practices and standards. * Proficiency in R programming language and other statistical software, including EAST. * Experience with CDISC, including SDTM, ADaM, CDASH. * Experience in representing sponsors in meetings with interaction with US FDA and international regulatory authorities. * Experience designing and conducting adaptive trials. Alnylam Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment. About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by "interfering" with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality. Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients.

The Analyst, Clinical Risk & Analytics (CRA) reports into the DSSE CRA function and is responsible for the delivery of timely and high-quality Centralized Monitoring activities, assessments and analytics for their assigned clinical trials in accordance with ICH GCP E6 requirement. Working closely with other CRA team members the Analyst will support the risk assessment and compliance with the protocol, ICH-GCP, and/or all applicable local and federal regulatory requirements to ensure patient safety and data integrity. Summary of Key Responsibilities The Analyst, Clinical Risk & Analytics (CRA) will; * Support other CRA team members, acting as RBQM Leads, in the identification and management of protocol, critical data and process, 'Critical to Quality' elements, safety and data integrity, and other protocol execution risks * Supports cross-functional study team and RBQM Leads in Protocol Risk Assessment, risk identification and evaluation into Risk MAP, as required. * Support RBQM Leads in selection and implementation of Key Risk Indicators (KRIs), and Quality Tolerance Limit parameters (QTLs) and other applicable assessments and dashboards for each study in the RBQM system, ensuring consistency with applicable standards. * Perform the set up and maintenance of the Risk-Based Quality Management (RBQM) system based on study teams requirements, data sources and structure Perform peer reviews, QC and or Validation of study setup in RBQM system vs RBQM Plan and system specifications, as required. * Work collaboratively with assigned Programmer to implement and refine study-specific KRIs and QTLs in the RBQM system * Performs, as required, the execution and review of the Study's assessments and analysis, and diagnosing and explaining anomalies identified in the data and risks * Deliver timely and high quality risk-based monitoring analytics and supports RBQM leads in communication to the cross-functional study team and CRO (both written report and oral presentation) to identify issue resolution as required * Support RBQM Leads during risk reviews sessions with cross-functional study team throughout clinical trials lifecycle * Ensure appropriate status and process documentation is produced and maintained during the study including study-specific validation * Communicate and/or escalate serious risks and issues to the cross-functional study team and/or management and Quality, as needed * Support RBQM Lead in conducting end of trial summarization of risk management activities, including QTL and other issue findings summaries, in preparation for inclusion to clinical study report. * Ensure inspection readiness for clinical risk management and centralized monitoring activities scope of activities * Champion RBQM within the company and participates in continuous improvement and development of risk management processes and system as needed Qualifications * Proven experience in a clinical research environment. * At least 3 years experience in a in a pharmaceutical/biologics/biotechnology company * Working knowledge of clinical development processes, understanding concepts and principles of study design, conduct and close out, as well as clinical program develop Skills * Familiarity and good understanding and knowledge of clinical trials risk management concepts and principles in the Pharma or CRO industry * Experience with data analytics and data visualisation technologies * Strong critical thinking and analytical skills and aptitude for data analytics including mathematical and statistical concepts * High degree of accuracy and attention to detail * Experience and understanding of clinical trial data from various sources (e.g. Clinical devices, SDTM, RAVE, IRT, etc) * Ability to work collaboratively in a team environment whilst managing changing priorities to achieve goals/targets. * Ability to build, develop, and maintain good working relationships with internal and external cross-functional customer groups. * Excellent English oral and written communication skills About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by "interfering" with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality. Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as the #1 Large Employer by Boston Globe Top Places to Work in 2023 for the third consecutive year, one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients. Qualified applicants will receive consideration for employment without regard to their race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, ethnicity, marital status, protected veteran status, disability, or any other characteristics prohibited by law.

Formulate Your Future Internship at EyePoint June 2 - August 8, 2025 Watertown, MA Be Seen and Heard at EyePoint At EyePoint, leadership trusts our employees to get the job done. The patient-centric and award-winning approach we're taking in business fuels our success for: preventing blindness through vision-saving medications delivering best-in-class proprietary pharmaceutical technologies transforming ocular drug delivery We See You. Your wellbeing Your professional worth Your future at EyePoint EyePoint offers a science-based entrepreneurial culture that empowers curiosity and innovation to help catapult your career. There's space for every voice and perspective to be heard in our on-site and remote environments where a variety of strengths and diverse backgrounds are connected. Formulate Your Future at EyePoint! Are you ready to turn your passion into experience? At EyePoint, we believe internships aren't just about coffee runs-they're about real-world impact, hands-on learning, and meaningful projects that set you up for success. As an EyePoint Intern, you will: • Dive into real projects that directly impact our business goals. • Collaborate with cross-functional teams to solve exciting challenges. • Attend community service events, and mentorship sessions. • Present your contributions to leadership at the end of your internship. Responsibilities The Summer Intern will report directly to a Process Engineer and will be responsible for supporting the manufacturing operations team at the Watertown, MA site. They will support several projects focused on new process development, continuous improvement of internal manufacturing processes, and process qualification for vision-saving drug-device combination products. Primary responsibilities and projects to be completed include the following: Identify and implement process improvements to support sites continuous improvement initiatives aimed at enhancing product quality, improving site safety standards, boosting operational efficiency, and minimizing waste. Author and execute equipment commission and qualification protocols (IQ/OQ/PQ) and reports. Create or revise process documentation, including standard operating procedures, work instructions, and batch records. Analyze development data and recommend new process development and/or changes to existing manufacturing processes. Collect and summarize in-process manufacturing data to support trending and statistical process control. Design, procure, and fabricate simple tooling and fixtures Support failure investigations, root cause analysis, and participate in corrective and preventative action efforts Source manufacturing equipment, and commission new equipment supporting semi-automated and automated solutions Qualifications Primary skills and knowledge required include, but are not limited to the following: Interest in/exposure to the Drug-Device Combination Product Industry Excellent communication skills, both written and oral Proficiency in the MS Office suite and familiarity with statistical analysis tools Experience in CAD platforms (SolidWorks/AutoCAD preferred) Strong foundational engineering and analytical skills Detail-oriented and well organized; strong willingness to learn Demonstrated ability to be a self-starter and work well on a team Working knowledge of current Good Manufacturing Practices (cGMP) and drug-device manufacture regulations, specifically FDA guidelines, is a bonus Level of Education Required: Must be a student in a Bachelor's degree program at an accredited college/university Undergraduate student with a minimum of Rising status. Preferred Field(s) of Study: Life sciences or similar science-based degree. Envision Your Future With the exciting energy of a winning culture and an exhilarating pace, we are an ophthalmology company committed to preventing blindness by developing and commercializing innovative therapeutics. The collective power of our values influences everything we do, and everything we do for you. Transformational Innovation We exist to change our patients' lives through the power of sight. We are forward looking, embrace challenges with curiosity, and continuously seek to improve our products and ourselves by learning, problem-solving and pushing the limits of science and technology. Unwavering Integrity We recognize our responsibility to our patients, employees, and our community, and value the trust they put in us. We set a high ethical bar and expect responsible leadership at every level to ensure we serve those who matter most to us. Compassionate Excellence We believe that fun and excellence can coexist. We foster a culture where enjoying the work we do and caring for each other are as important as delivering exceptional outcomes. Inclusive Collaboration We strive to see through the eyes of others and work as one team. We appreciate one another's differences and perspectives, and ensure everyone feels valued, respected and encouraged to bring their ideas forward. EyePoint Pharmaceuticals is proud to be an equal opportunity emp

This role is considered Hybrid. The Director, Enterprise Strategy will support and lead various strategy projects and strategic planning efforts with senior Alnylam leaders and the Executive Leadership Team including developing and refining mid-term and long-range corporate strategy at the enterprise level, as well as disease area strategies as our portfolio continues to grow. Projects will involve analysis across datasets, forecasts, identification and solutions for key strategic initiatives, guiding a strategic planning process and ensuring accountability for execution in line with our strategy. This individual will be a trusted thought partner to the VP Enterprise Strategy and Portfolio Analytics and the Chief Development and Strategy Officer, including proactively highlighting business critical risks/opportunities, identification of key issues and potential solutions prior in a timely manner, and developing, planning and directing the high priority organizational and operational activities for Enterprise effect. The individual must have the ability to context shift from a thought partner to an individual project leader to a team contributor. The ideal candidate will have the ability to thrive in uncertainty, take on challenges and work effectively in a matrix environment and with cross-functional teams, and be able to pivot quickly in response to rapidly changing business conditions. Thinking creatively by moving beyond process, driving data and analytics to landscape implications, and going from idea creation to tangible plans that create positive momentum will be critical to success. The role will require an ability to multi-task, prioritize multiple initiatives and develop solutions where blueprints may not exist. Familiarity with various strategy frameworks to develop plans that include the What, How and Why will be required as well as creative solving and innovation frameworks and methodologies. This position is hybrid and will be primarily located in Cambridge, MA. Key Responsibilities * Lead and support a variety of corporate and disease area strategy projects and strategic analysis, facilitating development of options and working across Alnylam leaders to gain buy-in. * Develop relationships and influence within a global matrixed organization and impact decision-making at the highest levels of the organization, while aligning across corporate and business lines for strategy harmonization * Apply various strategy frameworks, creative problem-solving approaches and other innovation methodologies to identify key strategic issues, appropriately frame them and drive development of potential solutions. * Design, plan and facilitate working sessions within the context of strategy projects aligning diverse perspectives and resulting in common direction across multiple functions. * Conduct competitive assessments and generate insights that may impact the strategic direction of the company * Research and maintain a deep understanding of competitors and scientific and clinical developments in si RNA, competitive technologies and disease areas * Identify opportunities to establish and continuously improve business practices to maximize resources and achieve operational excellence across multiple expertise areas * Aid in the strategic planning implications and outcomes associated with the company's Long Range Plan and scenario analysis based on possible outcomes for key assets. * Cultivate and maintain strong cross-functional relationships and contribute to our positive environment in support of our culture. Qualifications * Must have 7+ years experience in strategy / finance / operational roles * Prior pharma / biotech and management consulting experience including multiple years in a matrixed project leadership role, with preference for a drug development and/or early commercial background experience that included strategic responsibilities * Bachelor's Degree in Business or Finance required, MBA/PhD preferred with a strong scientific background * Strong leadership, problem solving, management and communication skills * Excellent interpersonal skills and ability to work effectively with multiple functions * Ability to lead and influence cross functional teams * Self-starter who can manage through ambiguity, learn on the fly, handle multiple priorities and perform job responsibilities accurately while working in a high energy, deadline-driven, and fast-paced environment * Possess the ability to generate enthusiasm, the ability to quickly gain trust and respect of peers and senior leadership and have a track record of successfully driving results through strong partnership with others About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by "interfering" with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality. Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we've been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as the #1 Large Employer by Boston Globe Top Places to Work in 2023 for the third consecutive year, one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients. Qualified applicants will receive consideration for employment without regard to their race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, ethnicity, marital status, protected veteran status, disability, or any other characteristics prohibited by law.

Formulate Your Future Internship at EyePoint June 2 - August 8, 2025 Watertown, MA Be Seen and Heard at EyePoint Pharmaceuticals At EyePoint, leadership trusts our employees to get the job done. The patient-centric and award-winning approach we're taking in business fuels our success for: preventing blindness through vision-saving medications delivering best-in-class proprietary pharmaceutical technologies transforming ocular drug delivery We See You. Your wellbeing Your professional worth Your future at EyePoint EyePoint offers a science-based entrepreneurial culture that empowers curiosity and innovation to help catapult your career. There's space for every voice and perspective to be heard in our on-site and remote environments where a variety of strengths and diverse backgrounds are connected. Formulate Your Future at EyePoint! Are you ready to turn your passion into experience? At EyePoint, we believe internships aren't just about coffee runs-they're about real-world impact, hands-on learning, and meaningful projects that set you up for success. As an EyePoint Intern, you will: • Dive into real projects that directly impact our business goals. • Collaborate with cross-functional teams to solve exciting challenges. • Attend community service events, and mentorship sessions. • Present your contributions to leadership at the end of your internship. We are seeking a motivated and detail-oriented FP&A (Financial Planning and Analysis) Intern to join our dynamic biotech team. This is a unique opportunity for a current student with a strong interest in finance and the biotechnology industry to gain hands-on experience in financial planning, forecasting, and analysis within a cutting-edge, fast-paced environment. Responsibilities Financial Modeling: Assist in building and maintaining financial models to support strategic decision-making, budgeting, and forecasting. Data Analysis: Gather, analyze, and interpret financial and operational data to identify trends, variances, and opportunities for improvement. Market Research: Support competitive and market trend analyses to inform strategic financial planning. Qualifications Strong analytical and quantitative skills, with proficiency in Excel). Excellent communication and presentation skills, with attention to detail. Interest in the biotechnology or pharmaceutical industry is strongly preferred. Benefits: Hands-on experience in a high-growth biotech company. Opportunity to develop financial and industry-specific expertise. Networking opportunities with professionals in finance and biotechnology. Level of Education Required: Must be a student in a Bachelor's degree program at an accredited college/university Undergraduate student with a minimum of Rising status. Preferred Field(s) of Study: Finance, Accounting, Economics, Business, or a related field. Envision Your Future With the exciting energy of a winning culture and an exhilarating pace, we are an ophthalmology company committed to preventing blindness by developing and commercializing innovative therapeutics. The collective power of our values influences everything we do, and everything we do for you. Transformational Innovation We exist to change our patients' lives through the power of sight. We are forward looking, embrace challenges with curiosity, and continuously seek to improve our products and ourselves by learning, problem-solving and pushing the limits of science and technology. Unwavering Integrity We recognize our responsibility to our patients, employees, and our community, and value the trust they put in us. We set a high ethical bar and expect responsible leadership at every level to ensure we serve those who matter most to us. Compassionate Excellence We believe that fun and excellence can coexist. We foster a culture where enjoying the work we do and caring for each other are as important as delivering exceptional outcomes. Inclusive Collaboration We strive to see through the eyes of others and work as one team. We appreciate one another's differences and perspectives, and ensure everyone feels valued, respected and encouraged to bring their ideas forward. EyePoint Pharmaceuticals is proud to be an equal opportunity employer. We believe that diversity and inclusion among our colleagues is critical to our success as a company, and we seek to recruit, develop, and retain the most talented people from a diverse candidate pool. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. #LI-Hybrid