Senior copywriter jobs in Massachusetts - 81 jobs

Job Title: Manager, Medical Writing Operations Pay: $76 an hour or about 156,000 a year Job Type: Long Term Contact The Manager, Medical Writing Operations supports Medical Writing functions to ensure the production of high-quality, submission-ready documents. This role oversees document quality, formatting, consistency, publishing, and archiving within central file systems. The position may also involve vendor oversight, staff training, and the development and maintenance of tools and training materials to enhance Medical Writing Operations. Key Responsibilities: Collaborate cross-functionally to collect, compile, assemble, and publish Clinical Study Report (CSR) appendices. Perform electronic publishing QC, including checking hyperlinks and bookmarks, to ensure submission readiness. Format MS Word submission components according to style and regulatory requirements; troubleshoot formatting issues. Serve as a subject matter expert (SME) for format QC, submission readiness (protocols, IBs, CSRs), and document management systems. Ensure documents are properly stored and archived in EDMS and eTMF systems. Conduct content QC of medical writing documents (e.g., CSRs, IB clinical sections, NDA/MAA clinical sections, protocols). Support creation, maintenance, and updates of templates, style guides, and tools to meet global regulatory requirements. Perform administrative tasks to support projects and operational needs. Participate in the development and maintenance of internal best practices. Assist in the development, implementation, and maintenance of medical writing systems and software. Provide training to internal staff and external contractors/CROs. Support vendor oversight for medical writing operations activities. Update Medical Writing intranet pages as needed. Assist with CSR shells and preparation of in-text tables and figures under medical writer guidance. Qualifications: Bachelor's degree in a relevant scientific/technical field or equivalent experience. 4+ years of experience in biotech/pharma or CRO settings with expertise in document QC and electronic publishing in a regulatory environment. Strong understanding of health authority/ICH PDF and eCTD requirements. Experience with electronic document management systems. Proven ability to manage multiple projects in a fast-paced, deadline-driven environment. Detail-oriented with strong analytical, problem-solving, and flexible skills. Ability and confidence to learn new software tools. Proficient in MS Word, Excel, PowerPoint, Adobe Acrobat, and Windows. Experience with StartingPoint templates, SharePoint, EndNote, and Toolbox Pharma preferred. Alignment with Alnylam Core Values: Commitment to People, Fiercely Innovative, Purposeful Urgency, Open Culture, and Passion for Excellence.

Industry: Pharmaceuticals Title: The Manager, Medical Writing Operations Duration: 12 months contract (+Possibility of extension) The Manager, Medical Writing Operations, provides support to Medical Writing functions to ensure high-quality, submission-ready documents. Responsibilities include document quality review, formatting and consistency, publishing, and archiving within central file systems. The role may also support vendor oversight, training, and the development and maintenance of tools and training materials for Medical Writing Operations. Key Responsibilities: Collaborate across functions to collect, compile, assemble, and publish CSR appendices Perform electronic publishing QC, including hyperlinks and bookmarks, to meet submission-ready guidelines Format MS Word submission components per style and regulatory requirements; troubleshoot formatting issues Serve as SME for format QC, submission readiness (protocols, IBs, CSRs), and document management systems Ensure documents are stored and archived appropriately in EDMS and eTMF systems Perform content QC of medical writing documents (eg, CSRs, IB clinical sections, NDA/MAA clinical sections, protocols) Support creation, maintenance, and updates of templates, style guides, and tools to meet global regulatory requirements Perform administrative tasks to support projects and operational needs Participate in development and maintenance of internal best practices Support development, implementation, and maintenance of medical writing systems and software Assist with training of internal staff and external contractors/CROs Support vendor oversight for medical writing operations activities Support updates to Medical Writing intranet pages as needed Assist with CSR shells and/or preparation of in-text tables and figures under medical writer oversight Qualifications • Bachelor's degree in a relevant scientific/technical field or equivalent experience4+ years of biotech/pharma or CRO experience in document QC and electronic publishing within a regulatory environment Strong understanding of health authority/ICH PDF and eCTD requirements Experience with electronic document management systems Proven ability to manage multiple projects in a fast-paced, deadline-driven environment Detail-oriented with strong analytical, problem-solving, and flexibility skills Ability and confidence to learn new software tools Proficient in MS Word, Excel, PowerPoint, Adobe Acrobat, and Windows Exposure to Starting Point templates, SharePoint, EndNote, and Toolbox Pharma preferred • Alignment with *** Core Values: Commitment to People, Fiercely Innovative, Purposeful Urgency, Open Culture, and Passion for Excellence

Senior Copywriter Cramer is a brand experience and content marketing agency. Cramer Health is a specialty division focused on providing content and experiences that educate and motivate patients, providers, and others in the healthcare ecosystem in actionable, meaningful ways. As part of Cramer Health's Content team, you'll research, develop, and refine content across media and channel for patients, pharmaceutical and healthcare professionals. You understand a brand's key messages and the nuances of its content - whether it's about navigating health insurance or supporting medication adherence. In this role, you'll work with a team to develop and maintain high quality content for pharmaceutical and medical device brands. This can include developing a wide array of content that can range from presentations and web pages to emails and letters. You can be writing for patient-facing audiences one minute and switching gears and preparing content for health provider offices the next. The role can be a mix of maintaining the accuracy of content across a hundred communications pieces already in market; to developing new content that can support thousands of patients as they start on a new treatment. You have to love the challenge of maintaining and creating content in equal measure. We are proud of our growth as an agency over the last 40 years and recently being named one of the Top Places to Work in 2022 by The Boston Globe. This is a full-time, in-office position based in Norwood, MA. Key Responsibilities: · Maintaining/developing high quality content driven by brand strategies and marketing goals · Knowledge and experience with medical, legal, and regulatory boards within pharmaceutical companies, including preparing annotations and references for medical/legal/regulatory submissions as needed · Using client brand guidelines to ensure our content is on-brand, on-message, and punctuation-perfect · Collaborating closely with teams - both internal and client members - to ensure that messaging and content deliverables ladder up to a strategy, are on-point for the audience, and will meet with regulatory guidelines and brand standards. Close collaboration with internal creative teams - and the ability to incorporate feedback quickly and accurately - are highly valued · Managing multiple projects simultaneously while meeting timelines · Comfortable with AI for fast iteration and style prompting but ready to uplevel with human intelligence and empathy. Requirements Requirements 4-5 years' experience as a professional writer in the medical and/or pharmaceutical space Experience preparing & representing content through the medical/legal/regulatory process Understanding of health insurance landscape is a plus Flexible self-starter who is willing to learn, adjust, and adapt Excellent communication and collaboration skills; open to feedback and guidance and able to give it other team members Meticulous attention to detail, and able to manage deliverable timelines in accordance with project delivery process Commitment to creating a world-class client experience Benefits Benefits Medical, Dental & Vision Insurance Health Savings Account, including employer contribution Retirement Plan (401K) with company match Profit Share Bonus Plan Life Insurance Paid Time Off Family Leave Short Term & Long-Term Disability Tuition Reimbursement Wellness Resources, including discounted membership to Lifetime Fitness Generous onsite café Paid holidays Salary Range: $90-110K

A Resume Writing & Job Search Strategy Company Our methodology is to deliver enhanced industry expertise and to service our customers as a team; this model coupled with our industry leading proprietary resume distribution engine and career search technologies set us apart. We provide clients with a bundled solution for career search excellence. Our clients tell us their new resume has opened doors to far more interviews and phone-calls from potential employers than they ever received before. Job Description Full Time / Salary + Benefits *Training provided in-house by experienced senior team The role: Currently searching for experienced writers to join our expanding in-house team. Experience writing for professionals and executives is an asset, but those with less than 2 years of writing experience are encouraged to apply. All training will be provided in-house on an ongoing basis, including working with senior writers. We are interested in hiring writers who can manage their time while maintaining a high standard of quality. Candidates with publishing experience and/or writing for professional organizations are also encouraged to apply. Duties: Writers will be working with our clientele to create individual resumes according to their career field, years of experience and related information that gives our clients a strong document for success in their job search. Skills and experience expected of a successful candidate: - Attention to detail and an ability to communicate well with our clients is essential. - Our clients receive a comprehensive consultation of about 45 minutes on average, therefore the ability to converse and hold interviews over the phone or in person will play a big part in putting together a compelling document. - Working on deadline is a must. Candidates will need to manage their workload and time to effectively meet deadlines and hold responsive communication with clients. - Excellent writing, editing, and proofreading skills, with the ability to draft clear and concise copy. Qualifications - Minimum of a Bachelor's Degree in Journalism or English and/or equivalent professional writing experience. - Accepting and adhering to high ethical, moral, and personal values in decisions, communications, actions, and when dealing with others. Additional Information How to apply: If you are interested in becoming part of our team please submit your resume and cover letter (all as MS Word attachments) plus no more than 3 writing samples.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Work with therapeutic teams to develop and/or edit scientific/clinical documents, including manuscripts, abstracts, posters, and slide presentations • Work effectively with company document management systems and related tools, templates, and procedures in order to ensure efficient internal and external review and approval of documents prior to final submission for publication or presentations at scientific congresses • Ensure a consistent style of writing and presentation of clinical data to maintain quality and ease of review by all contributing authors • Participate and contribute to Medical Affairs Publication Team meetings and to cross-functional working groups as needed to facilitate efficient development and submission of publications • Work with external and internal authors on company-sponsored publications to facilitate writing, review and submission to high-tier journals Skills: • Substantial experience (8-10 years) as a medical writer or equivalent working knowledge of clinical research, study design, and ability to present clinical data objectively in a clear, concise written format • Demonstrated competency in project management and the successful preparation and submission of peer-reviewed manuscripts • Outstanding written and verbal communication and interpersonal skills • Proficient in Word, Excel, PowerPoint, and Acrobat. Datavision expertise a plus • Highly organized, detail-oriented, self-motivated, and able to work independently as well as within cross-functional teams • Ability to manage multiple projects simultaneously, thinks critically, and adheres to deadlines • Demonstrated customer facing skills and capability to collaborate with Key Opinion Leaders on publications and presentations in a credible manner • Ability to interpret and critique scientific and medical literature with respect to scientific and business implications is essential • Experience in Multiple Sclerosis therapeutic or neurology area preferred • Medical writing or publications experience with a pharmaceutical company or medical communications agency preferred Qualifications • Advanced degree (MS, PhD, PharmD) in biomedical sciences is preferred, but not required Additional Information For more information, Please contact Akriti Gupta ************** Morristown, NJ 07960

We are a global medical communications agency blending deep scientific expertise with creative brilliance to inspire change. Behavior change starts with inspiration. By infusing vibrant creativity into our work, we produce engaging medical communications that have the power to captivate and spark action. Our absolute commitment to scientific precision across diverse therapy areas, including the complex fields of rare disease, oncology and advanced therapies, ensures we can make change a reality. For over 10 years, our team of exceptional PhD and advanced degree medical writers, strategists and world-class creatives has generated award-winning innovation across medical affairs and commercial disciplines. We are driven by a desire to create inspiring work that changes lives for the better, always guided by our core values - INTEGRITY, IMAGINATION, AGILITY, COLLABORATION and EMPOWERMENT - which underpin who we are and the positive culture of our team. Part of Synaptiq Health, our network also consists of market access & HEOR consultancy, Initiate, and healthcare PR specialist, Beyond PR. ROLE Could you be our next medical writer? In this role, you'll work across several accounts and therapy areas. You will develop engaging and accurate copy for selected healthcare communications projects covering scientific and branded communications. Joining the team offers a unique opportunity to contribute to a vibrant and rapidly growing US team. You'll be at the forefront of exciting projects, working collaboratively and playing a pivotal role in shaping the growth of our organization in this dynamic location. KEY RESPONSIBILITIES Write engaging, accurate and fully referenced content for selected accounts Act as an in-house therapy area expert in one or two disease areas Attend client and thought leader meetings and teleconferences, participating in content discussions as appropriate Develop and maintain excellent relationships with all departments and work collaboratively to produce high-quality communications Manage personal workload and schedules, actively responding to fluctuating business workloads Ensure all work allocated is executed within the timeline and schedule provided and accurately record all hours worked Be a brand guardian, both for our own company and our clients Perform other duties as assigned REQUIRED KNOWLEDGE, SKILLS AND ABILITIES At least 2 years' experience working within a medical communications agency Educated to postgraduate level in life sciences or a relevant area Therapy area experience in oncology, immunology or rare disease highly desirable Excellent attention to detail and ability to work simultaneously on more than one project Good knowledge and understanding of current US and international drug development processes Ability to provide realistic ideas for projects that deliver on clients' objectives Experience across various channels of healthcare communications Ability to write accurately and creatively in a fast-paced environment and to meet reasonable timelines Adaptability and flexibility to changing priorities Able to work independently and as part of a team Excellent verbal and written communication skills Ability to establish and maintain effective working relationships with co-workers, managers and clients Sound judgement and decision-making skills and the ability to determine when further supervision is needed Demonstrated ability to deliver results to the appropriate quality and timeline metrics Strong software and computer skills, including MS Office applications OUR REWARDS Comprehensive medical, dental and vision insurance plans (60% employer contribution) Access to 401(k) investment options, with an employer-matching contribution up to 4% A range of paid time-off benefits, including vacation leave, public holidays and sick leave We look forward to hearing from you!

Medical Writer - Oncology Clinical Trials Our Greater Boston area client is seeking an experienced Medical Writer with expertise in oncology clinical trials to support their growing clinical development programs. What You'll Do * Author and edit oncology trial documents (protocols, CSRs, IBs, IND/CTA sections, NDAs/BLAs). * Collaborate with clinical, regulatory, biostatistics, and safety teams. * Translate complex data into clear, compliant documents. * Ensure adherence to ICH-GCP, FDA/EMA guidelines, and SOPs. * Mentor contractors/junior writers as needed. What We're Looking For * Advanced degree (PhD, PharmD, MD, MSc). * 5+ years medical writing, 3+ in oncology. * Must have previous experience with clinical trial expansion plans, global study protocols, protocol amendments, and interim analysis reports. * Strong knowledge of oncology endpoints and regulatory submissions. * Excellent communication, detail orientation, and ability to manage deadlines. * Proficiency with MS Office, document systems, and style guides. Preferred * CRO/biotech/pharma experience. * Familiarity with eCTD submissions. * AMWA/EMWA membership. Apex Systems is a world-class IT services company that serves thousands of clients across the globe. When you join Apex, you become part of a team that values innovation, collaboration, and continuous learning. We offer quality career resources, training, certifications, development opportunities, and a comprehensive benefits package. Our commitment to excellence is reflected in many awards, including ClearlyRated's Best of Staffing in Talent Satisfaction in the United States and Great Place to Work in the United Kingdom and Mexico. Apex uses a virtual recruiter as part of the application process. Click here for more details. Apex Benefits Overview: Apex offers a range of supplemental benefits, including medical, dental, vision, life, disability, and other insurance plans that offer an optional layer of financial protection. We offer an ESPP (employee stock purchase program) and a 401K program which allows you to contribute typically within 30 days of starting, with a company match after 12 months of tenure. Apex also offers a HSA (Health Savings Account on the HDHP plan), a SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions, a corporate discount savings program and other discounts. In terms of professional development, Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Apex has a dedicated customer service team for our Consultants that can address questions around benefits and other resources, as well as a certified Career Coach. You can access a full list of our benefits, programs, support teams and resources within our 'Welcome Packet' as well, which an Apex team member can provide. Employee Type: Contract Location: Cambridge, MA, US Job Type: Date Posted: November 24, 2025 Pay Range: $90 - $150 per hour Similar Jobs * Contractor, Medical Affairs Operations * Contractor, Medical Publications Manager * IT Tech Writer * Tech Writer * Aviation Technical Publication Writer

At MFS, you will find a culture that supports you in doing what you do best. Our employees work together to reach better outcomes, favoring the strongest idea over the strongest individual. We put people first and demonstrate care and compassion for our community and each other. Because what we do matters - to us as valued professionals and to the millions of people and institutions who rely on us to help them build more secure and prosperous futures. THE ROLE The Investment Marketing Writer is an experienced financial writer who develops high-quality, insightful content that conveys MFS' investment expertise and insights. This role is integral in developing content for global marketing initiatives and MFS' thought leadership. Along with expert writing and editorial skills, this position requires an understanding of financial markets and investment products. WHAT YOU WILL DO Leverages writing expertise and knowledge of investment products and financial markets to produce high quality editorial content, providing input into the editorial strategy and broader Creative Services and Marketing strategies. Translates complex topics into clear, compelling and actionable content appropriate for each audience and aligned with MFS' brand. Develops, writes and edits marketing content including marketplace insights, corporate and product marketing materials, retail investment insights, white papers, brochures and flyers to support firm-wide and business channel campaigns. Supports MFS' digital platforms by writing original content and re-purposing existing content for web-based and social media platforms. Provides editorial consulting to internal groups in the form of copyediting, proofreading and project management. Helps ensure that MFS' voice and editorial style remain consistent across the firm. Collaborates with other teams within marketing, such as design, video, social media, paid media and client marketing, as well as Sales Enablement and other internal teams to ensure timely execution/production of marketing collateral to promote and position firm-wide enterprise themes internally and externally. Builds consensus across business areas. Maintains an understanding of capital markets, global macroeconomic trends and MFS' product offerings. Stays informed about industry trends to ensure content remains relevant and impactful. WHAT WE ARE LOOKING FOR BA/BS, or equivalent experience, in English, Economics, Finance or Marketing. Understanding of financial markets and investment products Minimum of 6-8+ years of professional writing experience, including at least 5 years of writing experience in an asset management company, or an agency serving the investment industry. Exceptional writing skills and demonstrated proficiency in writing for a variety of audiences. Editing and proofreading experience. Ability to work collaboratively with marketing colleagues and key stakeholders Ability to work on multiple projects while adhering to strict deadlines. Strong interpersonal and communication skills with a collaborative mindset. #LI-JN1 Base Salary Range: $107,000.00 - $154,000.00 This position is eligible for competitive incentive bonus. At MFS, we believe in fair and transparent compensation. For that reason, we're including the salary range for this position. This range reflects our good-faith expectation for what we'll pay depending on the candidate's experience, training and education. In addition to the salary, we also offer significant and competitive incentive compensation based on both individual and company performance. Other components of our Total Rewards Package include: MFS contributes an amount equal to 15% of your base salary to your retirement account that is separate from the company -sponsored 401(k) Education Assistance: MFS contributes $100 monthly up to $10,000 lifetime maximum directly to loan provider Education Assistance: Tuition reimbursement up to $8,000 annually Education Assistance: Access to discounted tutors and college coaches Generous time off and fully paid leaves including 20-weeks for maternity, 12-weeks for parental and caregiver leaves Choice of medical and dental plans and an and an employer contribution into the Health Savings Account Tax deferred commuter benefits & flexible spending accounts (medical & dependent care) Wellness Programs: Robust wellness webinars, employee assistance program with a focus on mental health, subsidized fitness benefit via Wellhub (formerly Gympass), where you can workout at gyms, studios and boutique fitness locations near you, join virtual personal training sessions and access a wide variety of well-being apps Our compensation philosophy is to pay competitively for talent while ensuring equity across employees performing comparable work. We are committed to transparency - if you have questions about how we arrived at this range or what additional benefits and bonus opportunities come with the role, we'll be happy to discuss them #LI-HYBRID At MFS, we are dedicated to building a diverse, inclusive and authentic workplace. If you are excited about this role but your past experience doesn't align perfectly, we encourage you to apply - you might be just the right candidate for this role or others. MFS is a hybrid work environment (remote/onsite) unless otherwise stated in the job posting. If any applicant is unable to complete an application or respond to a job opening because of a disability, please contact MFS at ************ or email talent_******************* for assistance. MFS is an Equal Opportunity Employer and it is our policy to not discriminate against any employee or applicant for employment because of race, color, religion, sex, national origin, age, marital status, sexual orientation, gender identity, genetic information, disability, veteran status, or any other status protected by federal, state or local laws. Employees and applicants of MFS will not be subject to harassment on the basis of their status. Additionally, retaliation, including intimidation, threats, or coercion, because an employee or applicant has objected to discrimination, engaged or may engage in filing a complaint, assisted in a review, investigation, or hearing or have otherwise sought to obtain their legal rights under any Federal, State, or local EEO law is prohibited. Please see the Know Your Rights: Workplace Discrimination is Illegal document, linked for your reference.

About the role: Advisor360°'s Product Adoption and Enablement team is looking for a Technical Writer to manage our product In-App help documentation and advise on other user-facing content. This writer will create and maintain help content in our CMS Paligo. We'd love to hear from you if you have strong documentation skills, consideration for your audience, and the ability to reflect the Advisor360° voice, tone, and style while still letting your own character shine through. Our ideal candidate is clever, collaborative, and driven by their curiosity to solve problems and celebrate solutions. We are very good at supporting each other and working across teams, and this role has a special place at the center of that network. We'll ask you for a couple of relevant writing samples with explanations of your content decisions. We'll also talk more about this during the interview. What You'll Do: Create and maintain clear, friendly, accessible help content, including screencaptures and videos. Create videos for user workflow simulations with Storylane. Strive to understand user needs and be an advocate for their success. Evaluate questions and responses using metrics to gauge success and identify gaps in our AI First Documentation. Contribute to the optimization of help content to increase accuracy and scope of AI chatbot's responses. Tracking In-App Help usage and engagement, with a goal to improve usefulness of chatbot Help responses. Consult website data and our customer-facing teams to inform content decisions. Work with our product management, development, and QA teams to understand and author content for new and existing features. Be an editorial resource for our developer documentation, UX copy, and other projects. Create reports and internal announcements for content updates and performance enhancements.. Who You Are: You have 5+ years of experience authoring documentation in fintech for enterprise level SaaS products with Paligo or similar XML or markdown based content management systems such as Oxygen and ReadMe. You have experience with tools like Jira, Confluence, Slack, Google Analytics, and Storylane. You've scripted, storyboarded, and produced videos with tools like Storylane, Camtasia, or the Adobe suite. You've explored site traffic data as an indicator for user behavior and content needs. A collaborative communicator with a willingness to learn and grow, as well as guide others. Your annoyed by mistakes in job postings and can't wait to provide editorial feedback in your cover letter. Extra points if you're familiar with Storylane, Figma, UserPilot, basic HTML and CSS, and technical concepts like, branching, APIs, SSO, and webhooks. Portfolio of work or website with writing samples must be provided. Why You'll Love Working Here: It's not just about work-it's about building a career and enjoying the ride! Here's what you can expect: We believe in recognizing and rewarding performance. Our compensation package includes competitive base salaries, annual performance-based bonuses, and the chance to share in the equity value you and your colleagues create during your time with the company. We offer comprehensive health benefits, including dental, life, and disability insurance. We also trust our employees to manage their time effectively, which is why we offer an unlimited paid time off program to help you perform at your best every day. Join us on this journey. Advisor360° is an equal opportunity employer committed to a diverse workforce. We believe diversity drives innovation and are therefore building a company where people of all backgrounds are truly welcome and included. Everyone is encouraged to bring their unique, authentic selves to work each and every day. The way we see it, we are here to learn from each other. The estimated base salary range for this position is $117,000 - $137,000 + bonus & equity. Advisor360° provides an estimate of the compensation for roles that may be hired as required by state regulations. Compensation may vary based on factors including, but not limited to, individual candidate experience, skills, and qualifications. Additionally, Advisor360° leverages current market data to determine compensation, therefore posted compensation figures are subject to change as new market data becomes available. The salary, other forms of compensation, and benefits information is accurate as of the date of this posting. Advisor360° reserves the right to modify this information at any time, subject to applicable law. While we are interested in qualified applicants who are permanently eligible to work for any employer in the United States, we are unable to sponsor or transfer sponsorship for employment visas at this time. To all recruitment agencies: We do not accept unsolicited agency resumes and are not responsible for any fees related to unsolicited resumes. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Senior Technical WriterEmployment Type: Full-Time, ExperiencedDepartment: Technology Support CGS is seeking an experienced Senior Technical Writer to provide consultative, analytical, and documentation support for a large Federal agency initiative. CGS brings motivated, highly skilled, and creative people together to solve the government's most dynamic problems with cutting-edge technology. To carry out our mission, we are seeking candidates who are excited to contribute to government innovation, appreciate collaboration, and can anticipate the needs of others. Here at CGS, we offer an environment in which our employees feel supported, and we encourage professional growth through various learning opportunities. Skills and attributes for success:- Drafting and development of technical documentation related to a variety of projects in the IT space.- Work closely with project stakeholders to establish technical processes and procedures.- Document projects through the SDLC.- Provide status reports for multiple ongoing projects and related documentation efforts.- Assist with both user and admin level documentation. Qualifications:- Excellent writing and Communication skills.- 5+ years experience with development of technical documentation.- 3+ years experience with development of user documentation.- Fluency with industry standard technical summary and reporting techniques including Agile project management methodology.- Ability to produce quality work independently or in a group setting.- Experience with MS Office Suite including Visio.- Willingness and ability to pass background check/security screening. Ideally, you will also have:- Familiarity with Business Intelligence/Analysis applications.- Experience with Government software development policies and procedures.- Client facing communication experience.- Federal Agency issued security clearance. Our Commitment:Contact Government Services (CGS) strives to simplify and enhance government bureaucracy through the optimization of human, technical, and financial resources. We combine cutting-edge technology with world-class personnel to deliver customized solutions that fit our client's specific needs. We are committed to solving the most challenging and dynamic problems. For the past seven years, we've been growing our government-contracting portfolio, and along the way, we've created valuable partnerships by demonstrating a commitment to honesty, professionalism, and quality work. Here at CGS we value honesty through hard work and self-awareness, professionalism in all we do, and to deliver the best quality to our consumers mending those relations for years to come. We care about our employees. Therefore, we offer a comprehensive benefits package.- Health, Dental, and Vision- Life Insurance- 401k- Flexible Spending Account (Health, Dependent Care, and Commuter)- Paid Time Off and Observance of State/Federal Holidays Contact Government Services, LLC is an Equal Opportunity Employer. Applicants will be considered without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Join our team and become part of government innovation! Explore additional job opportunities with CGS on our Job Board:**************************************** more information about CGS please visit: ************************** or contact: Email: ******************* #CJ

Clinical Operations

Department: Committee on Publication The Senior Writer and Editor is a member of the Editorial Activities team in the Office of Committee on Publication. This team's work is motivated and animated by the Church Manual Article XXXIII: “...to correct in a Christian manner impositions on the public in regard to Christian Science, injustices done Mrs. Eddy and members of this church….” As an integral part of a church office whose purpose is to lift and heal public thought, and to give humanity the opportunity to see Christian Science in its true light, the Senior Writer and Editor reports to the Editorial Activities Manager and works closely with other members of the Editorial Activities team. The senior Writer and Editor provides particular support to the Editorial Activities Manager. The work includes a daily commitment to the Christian Science healing practice, to seeing each occasion as a healing opportunity, and to approaching every aspect of the work “in a Christian manner.” The practical work includes but is not limited to writing and editing corrective responses for the media and academia, answering inquiries from the general public and church members, researching needed topics, working closely with Committees on Publication in various jurisdictions on corrective cases, and working to correct misinformation that appears on websites and in social media. This work may also include assisting with various short- and long-term projects, as well as direct contact with the public, including communication with media, giving talks to public groups, and meeting with scholars, authors, and students. ESSENTIAL DUTIES AND RESPONSIBILITIES Under the direction of the Editorial Activities Manager, the Senior Writer and Editor will be responsible for assisting in many areas of the Committee work: Gaining an understanding of the landscape or atmosphere of public thought as the context in which impositions on the public regarding Christian Science are addressed and healed; Praying specifically for healing of impositions and in support of essential activities in which the office and Committees in the field are engaged; Actively engaging with Committees on Publication in researching, writing, and/or editing corrective responses; Drafting content that provides information and guidance to Committees on Publication worldwide; Writing and/or editing corrective responses to Christian Science references in the media, academia, clergy, letters, books, etc., as well as responding to other outside correspondence and inquiries; Direct contact with the public, including communication with media, and - on occasion - giving talks to public groups, and meeting with scholars, authors, and students; Attending daily, weekly, and monthly staff meetings essential to advancing the corrective work of the office; this may include final preparation of an extensive document that is discussed during weekly corrective meetings; Contributing to the planning and facilitation of meetings with Committees on Publication; Leading the preparation, writing, and editing of regular Trends in Thought bulletins; Leading a team focused on correcting impositions on the public in regard to Christian Science presented on Wikipedia and other online encyclopedias; Responding to questions, drafting content, and helping to clarify issues in websites and social media pertaining to Christian Science; Contributing to the Manager's Office seasonal newsletters and other materials; Assisting with other projects as assigned. Reporting Relationships Supervisor : Reports to the Editorial Activities Manager Supervises: None Regular Contacts: This position has regular contact with the Editorial Activities Manager and other Editorial Activities team members; the Manager, Committees on Publication, other Manager's Office staff, and worldwide Committees on Publication. JOB REQUIREMENTS Education/Experience: A college degree or its equivalent. Substantial writing and editing experience; Knowledge/Skills This position requires excellent verbal and written communication skills; developmental and structural editing abilities; familiarity with copy editing; ability to manage priorities, meet deadlines, and track progress with both close collaboration and independent work. Spiritual maturity, discernment, good judgment, and teachability are also needed. Technology Skills: Gmail, Google Docs, Google Sheets, Google Slides, and basic familiarity with social media. Work Environment This position regularly works in an office environment at The Mother Church in Boston, MA. Christian Science Information Membership in The Mother Church and Primary Class instruction are required. Christian Science practice is helpful. Pay range: $100,541 - $130,702.40 annually The pay ranges disclosed in our job postings are the compensation ranges the Church reasonably and in good faith expects to pay for a given position at the time of posting. The offered salary will be determined by factors such as the applicant's relevant education, experience, knowledge, skills, abilities; and benchmarking, work location, and internal equity. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire.

About the Opportunity This job description is intended to describe the general nature and level of work being performed by people assigned to this classification. It is not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified . JOB SUMMARY The Senior Report Writer - Workday supports advanced reporting needs across Human Capital Management (HCM), Financials, and Student domains. This role is responsible for designing, building, and maintaining sophisticated Workday reports that provide actionable insights to leadership and help drive data-informed decision-making. Utilizes a broad and deep understanding of all areas of Workday Reporting & Analytics including Report Writer, Prism Analytics, Composite Reporting, BIRT, Calculated Fields, Dashboards, Discovery Boards, and Worksheets in providing professional services and enablement services for enterprise software in the Cloud. This role is hybrid and in the office a minimum of three days a week to facilitate collaboration and teamwork. In-office presence is an essential part of our on-campus culture and allows for engaging directly with staff and students, sharing ideas, and contributing to a dynamic work environment. Being on-site allows for stronger connections, more effective problem-solving, and enhanced team synergy, all of which are key to achieving our collective goals and driving success. *Applicants must be authorized to work in the United States. The University is unable to work sponsor for this role, now or in the future MINIMUM QUALIFICATIONS Knowledge and skills required for this position are normally obtained through a Bachelor's degree in data Analytics, Information Systems, Business Administration, or a related field with three (3) years hands-on experience building Workday reports across multiple domains (HCM, Finance, Payroll). Workday Certification in at least one of the following: Workday Financials, Workday Reporting, Advanced Reporting required. Proficiency in Workday reporting tools, including Advanced, Matrix, Composite, and BIRT reports required. Strong understanding of Workday data structures, business processes, and security models needed. Experience with data visualization tools or Workday Prism Analytics a plus. KEY RESPONSIBILITIES & ACCOUNTABILITIES 1) Design and develop complex custom reports in Workday using Advanced, Matrix, Composite, Trending, and BIRT (Business Intelligence and Reporting Tools) reports. 2) Partner with HR, Finance, Student Services, and Institutional Research teams to support operational and strategic reporting needs including translating requirements to deliver accurate and meaningful reports 3) Build dashboards and scorecards using Workday Prism Analytics, Workday Discovery Boards (if available), and other Workday tools. 4) Maintain reporting documentation, data dictionaries, and metadata to support institutional transparency and reusability. 5) Troubleshoot and resolve issues related to reporting performance, data discrepancies, and user access and proactively identify opportunities to improve data accessibility and self-service through training. Position Type Data Planning and Analysis Additional Information Northeastern University considers factors such as candidate work experience, education and skills when extending an offer. Northeastern has a comprehensive benefits package for benefit eligible employees. This includes medical, vision, dental, paid time off, tuition assistance, wellness & life, retirement- as well as commuting & transportation. Visit ************************************* for more information. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to race, religion, color, national origin, age, sex, sexual orientation, disability status, or any other characteristic protected by applicable law. Compensation Grade/Pay Type: 110S Expected Hiring Range: $75,210.00 - $106,230.00 With the pay range(s) shown above, the starting salary will depend on several factors, which may include your education, experience, location, knowledge and expertise, and skills as well as a pay comparison to similarly-situated employees already in the role. Salary ranges are reviewed regularly and are subject to change.

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. This is Contract position with my direct client Job Description Overview: The Medical Writer Specialist is responsible for preparation of documents that support the presentation and/or publication needs of assigned therapeutic areas and/or medical devices in the Client Strategic Medical Affairs Team for a wide range of audiences. Key Job Activities: Primarily focuses on preparing, writing, editing, and reviewing regulatory (e.g. Clinical Evaluation Reports (CERs), clinical data reports or summaries) documents and responses to regulatory authorities (e.g. notified bodies). Participates in post-market surveillance activities by conducting routine systematic literature reviews (e.g. screens articles against inclusion/exclusion criteria, extracts data from included studies, interprets study results, synthesizes literature, and prepares summaries into formal reports) for specific medical device groups or sub-groups. Performs scientific writing (e.g. abstracts, manuscripts, presentations). Organizes and incorporates information for documents, such as references, graphics, tables, and data listings. Ensures documents are produced in accordance with procedures, internal and external guidelines (e.g. MEDDEV 2.7.1), and electronic templates. Ability to quickly acquire understanding of therapeutic areas, medical device portfolios, business objectives, clinical data/evidence Independently, critically writes and edits scientifically complex documents for substantial intellectual content. Reviews and provides input on clinical data being considered for presentation and/or publication to ensure alignment with scientific strategies and corporate goals. Expert knowledge of clinical research, device/drug development processes, regulatory requirements, good clinical and data management practices. Ability to understand and interpret statistical results of clinical studies; specifically summarize complex results and present them in clear, concise, and scientifically accurate manner to various end users. Communicates with various departments (e.g. Regulatory, Product Development, Clinical Research, Quality) to identify the necessary clinical and technical information. Qualifications Job Qualifications Education Ph.D/Pharm D plus 1 to 2 years of related medical device/drug industry experience (e.g. medical writing, regulatory affairs, clinical research, engineering) BS/B.Pharm/BSN or MS or MPH plus 4 to 5 years of relevant medical device/drug industry experience Knowledge/Requirements Excellent English language skills, especially writing and proofreading. Clinical, scientific or research background, highly preferred. Experience writing CERs, highly preferred. Knowledge in narrative or systematic literature reviews (e.g. PRISMA, Cochrane), highly preferred. Experience in medical writing or demonstration in scientific writing ability in accordance with International Committee of Medical Journal Editors (ICMJE) authorship guidelines, preferred. Expert understanding of scientific or clinical research and methods. Understanding of statistical data and good data management practices. Strong oral communication, presentation, project management and prioritization skills. Excellent interpersonal relationships. Highly proficient in Microsoft Office Suite and bibliographic software (e.g. Endnote, Reference Manager). Additional Information Contact me at 732 549 5307

A Resume Writing & Job Search Strategy Company Our methodology is to deliver enhanced industry expertise and to service our customers as a team; this model coupled with our industry leading proprietary resume distribution engine and career search technologies set us apart. We provide clients with a bundled solution for career search excellence. Our clients tell us their new resume has opened doors to far more interviews and phone-calls from potential employers than they ever received before. Job Description Full Time / Salary + Benefits *Training provided in-house by experienced senior team The role: Currently searching for experienced writers to join our expanding in-house team. Experience writing for professionals and executives is an asset, but those with less than 2 years of writing experience are encouraged to apply. All training will be provided in-house on an ongoing basis, including working with senior writers. We are interested in hiring writers who can manage their time while maintaining a high standard of quality. Candidates with publishing experience and/or writing for professional organizations are also encouraged to apply. Duties: Writers will be working with our clientele to create individual resumes according to their career field, years of experience and related information that gives our clients a strong document for success in their job search. Skills and experience expected of a successful candidate: - Attention to detail and an ability to communicate well with our clients is essential. - Our clients receive a comprehensive consultation of about 45 minutes on average, therefore the ability to converse and hold interviews over the phone or in person will play a big part in putting together a compelling document. - Working on deadline is a must. Candidates will need to manage their workload and time to effectively meet deadlines and hold responsive communication with clients. - Excellent writing, editing, and proofreading skills, with the ability to draft clear and concise copy. Qualifications - Minimum of a Bachelor's Degree in Journalism or English and/or equivalent professional writing experience. - Accepting and adhering to high ethical, moral, and personal values in decisions, communications, actions, and when dealing with others. Additional Information How to apply: If you are interested in becoming part of our team please submit your resume and cover letter (all as MS Word attachments) plus no more than 3 writing samples.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Work with therapeutic teams to develop and/or edit scientific/clinical documents, including manuscripts, abstracts, posters, and slide presentations • Work effectively with company document management systems and related tools, templates, and procedures in order to ensure efficient internal and external review and approval of documents prior to final submission for publication or presentations at scientific congresses • Ensure a consistent style of writing and presentation of clinical data to maintain quality and ease of review by all contributing authors • Participate and contribute to Medical Affairs Publication Team meetings and to cross-functional working groups as needed to facilitate efficient development and submission of publications • Work with external and internal authors on company-sponsored publications to facilitate writing, review and submission to high-tier journals. Qualifications Substantial experience (8-10 years) as a medical writer or equivalent working knowledge of clinical research, study design, and ability to present clinical data objectively in a clear, concise written format • Demonstrated competency in project management and the successful preparation and submission of peer-reviewed manuscripts • Outstanding written and verbal communication and interpersonal skills • Proficient in Word, Excel, PowerPoint, and Acrobat. Datavision expertise a plus • Highly organized, detail-oriented, self-motivated, and able to work independently as well as within cross-functional teams • Ability to manage multiple projects simultaneously, thinks critically, and adheres to deadlines • Demonstrated customer facing skills and capability to collaborate with Key Opinion Leaders on publications and presentations in a credible manner • Ability to interpret and critique scientific and medical literature with respect to scientific and business implications is essential • Experience in Multiple Sclerosis therapeutic or neurology area preferred • Medical writing or publications experience with a pharmaceutical company or medical communications agency preferred Education: • Advanced degree (MS, PhD, PharmD) in biomedical sciences is preferred, but not required Additional Information For more information, please contact Sneha **************

We are a global medical communications agency blending deep scientific expertise with creative brilliance to inspire change. Behavior change starts with inspiration. By infusing vibrant creativity into our work, we produce engaging medical communications that have the power to captivate and spark action. Our absolute commitment to scientific precision across diverse therapy areas, including the complex fields of rare disease, oncology and advanced therapies, ensures we can make change a reality. For over 10 years, our team of exceptional PhD and advanced degree-educated medical writers, strategists and world-class creatives have generated award-winning innovation across medical affairs and commercial disciplines. We are driven by a desire to create inspiring work that changes lives for the better, always guided by our core values - INTEGRITY, IMAGINATION, AGILITY, COLLABORATION and EMPOWERMENT - which underpin who we are and the positive culture of our team. ROLE Could you be our next Principal Medical Writer? In this role, you'll act as the scientific lead across a number of accounts and therapy areas to steer content strategy and delivery. You will create engaging and scientifically accurate content for healthcare communications projects and review work produced by other team members to ensure all outputs meet the highest quality standards. You'll also help lead proposals and pitches for your accounts and/or potential new clients in key therapy areas. Joining this team offers a unique opportunity to contribute to the growth and development of our US presence. You'll be at the forefront of exciting projects, playing a pivotal role in shaping the future and helping expand our operations in this dynamic location. If you're eager to make an impact and be part of something transformative, this is the perfect chance to help build and influence the success of our Boston team. KEY RESPONSIBILITIES Own and manage content projects through independently developing and writing engaging, accurate and fully referenced content for a wide variety of accounts and medical materials including print, digitial applications, internal communications and meeting materials Serve as scientific lead on medium and large sized account(s), guiding and overseeing scientific content and strategic direction Lead proposals and business development efforts as appropriate, including within your designated accounts Attend client and thought-leader meetings and teleconferences, leading on content discussions as appropriate and maintaining strong client relationships Develop and maintain excellent relationships with all other departments, and collaboratively work with the design, development and accounts teams to produce high-quality communications Assist in managing team workloads by advising on priorities, balancing resources and responding to shifting business needs Proactively assess and contribute toward optimising ways of working within the medical team and independently oversee and implement best practices Be a brand guardian, both for our own company brand as well as for our clients Ensure all work allocated is executed within the timeline and schedule provided and to record all hours worked accurately Perform other duties as assigned REQUIRED KNOWLEDGE, SKILLS AND ABILITIES At least 4-6 years of experience working within a medical communications agency Educated to degree or post-graduate level in life sciences or relevant area Therapy area experience in oncology is highly desirable Excellent attention to detail and ability to work simultaneously on more than one project Good knowledge and understanding of current international life sciences arena Ability to provide realistic ideas for projects which deliver on client's objectives Experience across various channels of healthcare communications Ability to write accurately and creatively in a fast-paced environment and to meet reasonable timelines Adaptability and flexibility to changing priorities Able to work as part of a team or solo Excellent verbal and written communication Ability to establish and maintain effective working relationships with co-workers, managers and clients Sound judgement and decision making skills with ability to distinguish when further supervision is needed Demonstrated ability to deliver results to the appropriate quality and timeline metrics Strong software and computer skills, including MS Office applications OUR REWARDS Comprehensive medical, dental, and vision insurance plans (60% employer contribution) Access to 401(k) investment options, with an employer matching contribution up to 4% A range of paid time off benefits, including vacation leave, public holidays and sick leave We look forward to hearing from you!

Job DescriptionSenior Technical WriterEmployment Type: Full-Time, ExperiencedDepartment: Technology Support CGS is seeking an experienced Senior Technical Writer to provide consultative, analytical, and documentation support for a large Federal agency initiative. CGS brings motivated, highly skilled, and creative people together to solve the government's most dynamic problems with cutting-edge technology. To carry out our mission, we are seeking candidates who are excited to contribute to government innovation, appreciate collaboration, and can anticipate the needs of others. Here at CGS, we offer an environment in which our employees feel supported, and we encourage professional growth through various learning opportunities. Skills and attributes for success:- Drafting and development of technical documentation related to a variety of projects in the IT space.- Work closely with project stakeholders to establish technical processes and procedures.- Document projects through the SDLC.- Provide status reports for multiple ongoing projects and related documentation efforts.- Assist with both user and admin level documentation. Qualifications:- Excellent writing and Communication skills.- 5+ years experience with development of technical documentation.- 3+ years experience with development of user documentation.- Fluency with industry standard technical summary and reporting techniques including Agile project management methodology.- Ability to produce quality work independently or in a group setting.- Experience with MS Office Suite including Visio.- Willingness and ability to pass background check/security screening. Ideally, you will also have:- Familiarity with Business Intelligence/Analysis applications.- Experience with Government software development policies and procedures.- Client facing communication experience.- Federal Agency issued security clearance. Our Commitment:Contact Government Services (CGS) strives to simplify and enhance government bureaucracy through the optimization of human, technical, and financial resources. We combine cutting-edge technology with world-class personnel to deliver customized solutions that fit our client's specific needs. We are committed to solving the most challenging and dynamic problems. For the past seven years, we've been growing our government-contracting portfolio, and along the way, we've created valuable partnerships by demonstrating a commitment to honesty, professionalism, and quality work. Here at CGS we value honesty through hard work and self-awareness, professionalism in all we do, and to deliver the best quality to our consumers mending those relations for years to come. We care about our employees. Therefore, we offer a comprehensive benefits package.- Health, Dental, and Vision- Life Insurance- 401k- Flexible Spending Account (Health, Dependent Care, and Commuter)- Paid Time Off and Observance of State/Federal Holidays Contact Government Services, LLC is an Equal Opportunity Employer. Applicants will be considered without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Join our team and become part of government innovation! Explore additional job opportunities with CGS on our Job Board:**************************************** more information about CGS please visit: ************************** or contact: Email: ******************* #CJ We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Work with therapeutic teams to develop and/or edit scientific/clinical documents, including manuscripts, abstracts, posters, and slide presentations • Work effectively with company document management systems and related tools, templates, and procedures in order to ensure efficient internal and external review and approval of documents prior to final submission for publication or presentations at scientific congresses • Ensure a consistent style of writing and presentation of clinical data to maintain quality and ease of review by all contributing authors • Participate and contribute to Medical Affairs Publication Team meetings and to cross-functional working groups as needed to facilitate efficient development and submission of publications • Work with external and internal authors on company-sponsored publications to facilitate writing, review and submission to high-tier journals. Skills: • Substantial experience (8-10 years) as a medical writer or equivalent working knowledge of clinical research, study design, and ability to present clinical data objectively in a clear, concise written format • Demonstrated competency in project management and the successful preparation and submission of peer-reviewed manuscripts • Outstanding written and verbal communication and interpersonal skills • Proficient in Word, Excel, PowerPoint, and Acrobat. Datavision expertise a plus • Highly organized, detail-oriented, self-motivated, and able to work independently as well as within cross-functional teams • Ability to manage multiple projects simultaneously, thinks critically, and adheres to deadlines • Demonstrated customer facing skills and capability to collaborate with Key Opinion Leaders on publications and presentations in a credible manner • Ability to interpret and critique scientific and medical literature with respect to scientific and business implications is essential • Experience in Multiple Sclerosis therapeutic or neurology area preferred • Medical writing or publications experience with a pharmaceutical company or medical communications agency preferred Qualifications • Advanced degree (MS, PhD, PharmD) in biomedical sciences is preferred, but not required Additional Information For more information, please contact Akriti Gupta ************** Morristown, NJ 07960