Senior Copywriter
Medical writer job in Chicago, IL
Who We Are:
Old Republic is a leading specialty insurer that operates diverse property & casualty and title insurance companies. Founded in 1923 and a member of the Fortune 500, we are a leader in underwriting and risk management services for business partners across the United States and Canada. Our specialized operating companies are experts in their fields, enabling us to provide tailored solutions that set us apart.
Position Overview:
The Senior Copywriter will serve as a lead storyteller for Old Republic and its family of companies, crafting engaging, brand-aligned content that strengthens visibility, builds trust, and supports enterprise marketing initiatives. This role combines creativity with strategy, bringing clarity and personality to complex topics across a range of industries and audiences.
Essential Job Functions:
Craft and refine messaging: Write, edit, and proof compelling copy for start-up operating companies, the shares services model, and holding company initiatives.
Translate complexity into clarity: Transform technical and industry-specific language into clear, engaging messages tailored to target audiences.
Shape brand voice: Help develop and maintain tone of voice guidelines to ensure consistency across all materials and communication channels.
Lead content creation: Drive the timely development and execution of marketing deliverables across digital, print, web, social, and event channels.
Contribute to campaign strategy: Collaborate with marketing and creative teams to shape campaign messaging, creative concepts, and copy direction.
Execute content strategy: Collaborate with the marketing team to manage a content calendar that supports long-term storytelling, promotional planning, and campaign execution.
Steward brand consistency: Establish and manage company-wide editorial and writing standards; partner with Legal and Compliance teams for review and governance.
Manage content pipeline: Oversee content requests, project prioritization, and coordination with internal teams and external agencies.
Qualifications:
Bachelor's degree in Marketing, Communications, Journalism, English, Public Relations, or a related field preferred.
8+ years of experience as a copywriter, editor, or journalist, ideally within financial services or insurance.
Demonstrated ability to write clear, concise, and grammatically precise copy across formats - advertising, web, social, print, and digital campaigns.
Proven ability to adapt writing style and tone for diverse audiences and industries.
Strong editorial judgement and attention to detail; excellent proofreading and editing skills.
Experience developing and managing integrated marketing communications plans (e.g., campaigns, digital and social content).
Working knowledge of content management and marketing automation platforms; HubSpot experience preferred.
Familiarity with SEO principles, accessibility standards (WCAG), and CRM-driven communication strategies a plus.
Strong organizational and project management skills; able to manage multiple priorities and meet deadlines.
A portfolio demonstrating a range of writing styles and master of brand voice is required.
ORI is an Equal Opportunity Employer. ORI provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
Technical Writer
Medical writer job in Batavia, IL
Suncast Corporation is the leading US-based designer, manufacturer, and distributor of high-quality resin products for the home and industrial markets. A privately held company headquartered in Western Chicago, Illinois, Suncast prides itself on 35 years of innovation and sustainability across a wide range of product categories with materials proudly sourced in the USA. Everything we do is supported by the strength and ingenuity of American workers and we are committed to helping families across the country make the most of their unique spaces. We utilize state-of-the-art machinery and innovative manufacturing techniques to consistently engineer products of the highest possible quality.
Summary:
The Technical Illustrator is responsible for developing and updating all product instruction manuals. The candidate will assist in overseeing relationships with print and other third-party suppliers to ensure we meet production deadlines. Interaction with various supporting departments (Purchasing, Legal, Customer Service, Sales, and Marketing) requires clear and proactive communication. A meticulous attention to detail is crucial, along with the ability to create visuals that communicate effectively.
Responsibilities:
The following duties are considered essential to this position. Other responsibilities may be assigned.
Development of product instruction manuals and updating of existing manuals
Manual content, planning and sequencing.
Development of installation and operating instructions using isometric views with insets and bubbles as needed.
Manual development for multiple languages utilizing internal and external translations resources.
The ability to assemble and evaluate products to ensure manual accuracy and completeness.
Partnering with the Purchasing Department for the evaluation and awarding of print and third-party illustrator contracts.
Managing and monitoring supplier performance related to the creation, development, and printing of Suncast manuals.
Ensuring that manuals are properly reviewed and approved, with sign-off, prior to printing.
Manual revision management including tracking active revisions, in progress revisions, archiving of manuals.
Stay informed and make recommendations on changes and trends related to product manuals.
Integrate feedback from other business units to improve manuals.
Prioritize manual creation and revisions to meet varied production deadlines.
Support and comply with safety policies, quality standards, and housekeeping methods.
Ensure that manuals are compliant with product safety commission requirements and any other regulations.
Qualifications:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Bachelor's degree is preferred, but not required. Minimum of a two-year diploma from an accredited community or technical college, in Technical Illustration or Technical Communication.
Minimum of 3+ years' experience in technical writing and technical illustration, including demonstrated experience managing technical product manuals.
Strong writing and communication skills in English required. Technical writing skills required.
Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations.
Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. Ability to work under strict deadlines. Possess information management skills. Must have sharp eye for detail.
While performing this job, the employee will use a computer extensively. This includes Microsoft Windows, Microsoft Office, 3D CAD software, Adobe Creative Suite, SolidWorks Composer, change control software, workflows, and tools to transmit large files.
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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this position, the employee will divide his or her time between working on product assembly and evaluation in the manufacturing area or developing manuals in an office environment. The employee is required to stand, walk, climb, stoop, or kneel. The employee may need to occasionally lift and/or move up to 35 pounds. While writing reports the employee is required to sit, use a computer with a keyboard and mouse, talk, and hear. Vision requirements include ability for close vision so printed reports and computer screens can be read, distance vision, and the ability to focus. Color acuity is a plus.
Work Environment:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing these duties, the employee will spend part of his or her time in a manufacturing environment, and part of the time in an office environment. Manufacturing areas are subject to seasonal variations in temperature. Noise level is generally moderate for manufacturing. Safety equipment is required when in manufacturing areas. Typically, offices are climate controlled and have a moderate noise level for an office.
The Anticipated Pay Range for This Position: $80-95K annually
Suncast offers a comprehensive benefits package including:
Medical, Dental, and Vision insurance
Telehealth benefits
Life insurance
401K with employer match
Paid vacation time off
Paid parental leave
Short- and long-term disability coverage
Health Savings Accounts (HSAs) & Flexible Spending Accounts (FSAs) for health and dependent care
Paid Parental Leave (maternity & paternity)
Educational Assistance Program
Tuition Reimbursement
Medical Writer II
Medical writer job in Des Plaines, IL
Author technical documents with a high level of detail and precision to support domestic and international regulatory submissions.
Incorporate graphs, charts, tables, and statistical analyses from approved source files.
Proofread, edit, circulate, assemble, and inspect submission documents for accuracy and compliance. Focus Area: This role is primarily focused on EU IVDR submissions.
Qualifications:
3- 5 years of experience in medical writing or regulatory documentation.
Strong skills in preparing and editing scientific reports.
Ability to work with complex data and present it clearly in technical documents
Consultants Eligible Benefits Upon Waiting Period:
Medical and Prescription Drug Plans
Dental Plan
Vision Plan
Health Savings Account (for High-Deductible Health Plans)
Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
Supplemental Life Insurance
Short Term Disability (coverage varies by state)
Long Term Disability
Critical Illness, Hospital coverage, Accident Insurance
MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
401(k)
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.
Medical Writer
Medical writer job in Chicago, IL
Reporting directly to the Vice President of Clinical Development, the Medical Writer will be responsible for leading and executing all medical writing activities supporting Xeris' clinical programs. The individual will have a strong scientific background, exceptional writing skills, and a proven ability to translate complex clinical and scientific data into clear, accurate, and regulatory-compliant documents tailored to diverse audiences.
**Responsibilities**
+ Develop and authora broad range of clinical and regulatory documents, including but not limited to: clinical study protocols, investigator brochures (IBs), clinical study reports (CSRs), and sections of regulatory submissions (e.g., IND, NDA, etc.).
+ Ensure accuracy, clarity, consistency, and compliancewith internal standards, applicable regulatory guidelines (e.g., ICH, FDA, EMA), and company SOPs.
+ Collaborate cross-functionallywith colleagues in Clinical, Regulatory Affairs, Medical Affairs, and other internal stakeholders to gather relevant data and ensure consistency of messaging across documents.
+ Translate highly technical and statistical informationinto clear, concise content suitable for a wide variety of audiences including regulators, healthcare professionals, and non-scientific business leaders, as required.
+ Contribute to the development of communication materials, including slide decks, manuscripts, abstracts, and presentations, to support internal and external scientific communications.
+ Maintain document quality controlthrough proofreading, editing, and adherence to templates, style guides, and version control procedures.
+ Manage timelines and priorities for multiple projects simultaneously, ensuring timely and accurate delivery of high-quality documents.
+ Provides detailed medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copy editing and content review.
+ Ensures document content and style adheres to FDA/EMA or other appropriate regulatory guidelines and complies with departmental SOPs and style guidelines.
+ Performs literature searches and reviews as necessary to obtain background information and provide literature references.
+ Provide input on processes, templates, and other business needs within the medical writing function.
+ Coordinate and/or manage review cycles to triage, incorporate, and resolve team comments, and lead discussion on document revision and finalization for both internally written and outsourced documents.
+ Serve as a point person for medical writing guidance and document-related problem resolution.
**Qualifications**
+ Bachelor's degree in Life Sciences or a related field is required; advanced degree (PhD, PharmD, or MS) strongly preferred.
+ Minimum of 5 years of medical writing experience in the pharmaceutical, biotechnology, or clinical research industry, with a focus on late-stage clinical development (Phase 3).
+ Demonstrated experience in writing regulatory submission documents in compliance with regulatory agency guidelines.
+ Proficiency in Microsoft Office Suite and familiarity with document management systems and version control tools.
+ Competencies: Attention to Detail, Organizational skills, Adaptability, Multi-Tasking, Strong Written & Verbal Communication skills, Independent Judgement, Cross-Team Collaboration, Critical Thinking, Problem Solving
+ Working Conditions:Position may require periodic evening and weekend work, as necessary to fulfill obligations. Periodic overnight travel. _This is a hybrid position located in Xeris' Chicago office and requires three days per week on-site. On-site requirement may change at management's discretion._
_The level of the position will be determined based on the selected candidate's qualifications and experience._
\#LI-HYBRID
_As an equal employment opportunity and affirmative action employer, Xeris Pharmaceuticals, Inc. does not discriminate on the basis of race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, veteran status, genetics or any other characteristic protected by law. It is our intention that all qualified applications are given equal opportunity and that selection decisions be based on job-related factors._
_The anticipated base salary range for this position is $75,000 to $150,000. Final determination of base salary offered will depend on several factors relevant to the position, including but not limited to candidate skills, experience, education, market location, and business need. This role will include eligibility for bonus and equity. The total compensation package will also include additional elements such as multiple paid time off benefits, various health insurance options, retirement benefits and more. Details about these and other offerings will be provided at the time a conditional offer of employment is made. Candidates are always welcome to inquire about our compensation and benefits package during the interview process._
_NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization._
**Job Locations** _US-IL-Chicago_
**Title** _Medical Writer_
**ID** _2025-2296_
**Category** _Clinical Development_
**Type** _Full-Time_
Senior Medical Writer (Project-Based)
Medical writer job in Chicago, IL
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
Our mission is to deliver high-quality service and technology solutions - rooted in strong science and decades of regulatory experience - that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit ******************* or follow MMS on LinkedIn.
This role is a remote, project-based consulting opportunity.
Responsibilities
Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias
Write and edit clinical development documents, including but not limited to, clinical protocols, investigator's brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals
Complete writing assignments in a timely manner
Maintain timelines and workflow of writing assignments
Practice good internal and external customer service
Highly proficient with styles of writing for various regulatory documents
Expert proficiency with client templates & style guides
Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects
Contribute substantially to, or manages, production of interpretive guides
Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary
Mentor medical writers and other members of the project team who are involved in the writing process
Requirements
At least 3 years of previous experience in the pharmaceutical industry
Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience
The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline
Substantial clinical study protocol experience as lead author
Experience leading and managing teams while authoring regulatory documents with aggressive timelines
Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus
Understanding of clinical data
Exceptional writing skills are a must
Excellent organizational skills and the ability to multi-task are essential prerequisites
Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools
Experience being a project lead, or managing a project team
Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus
Auto-ApplyScientific Writer
Medical writer job in Chicago, IL
Department
PSD Data Science: NITMB Group
About the Department
The NSF-Simons National Institute for Theory and Mathematics in Biology (NITMB) is a partnership between Northwestern University and the University of Chicago. The institute aims to integrate the disciplines of mathematics and biology in order to transform the practice of biological research and to inspire new mathematical discoveries. The staff at NITMB support the community of scholars, the shared ideals, and the core values of the institute. Together with the University of Chicago and Northwestern University, the NITMB provides the opportunities, infrastructure, and resources that encourage our faculty and other scholars to pursue their finest work.
Job Summary
This role involves creating various communications for the National Institute of Theory and Mathematics in Biology. The Scientific Writer will research and assist in writing articles and reports for the Research faculty, the Fellows, and help with reports for outside evaluations. This includes advising on writing blog posts and public-facing articles about the research coming out of the NITMB. The Scientific Writer will report to the Deputy Director for Research at the NITMB. This position will produce feature articles, requests for information (RFI), reports for University stakeholders and philanthropic organizations, along with other print and online communications. Under moderate guidance, the individual will research, compose, and edit high-level communications, publications, and reports on complex and specialized subjects.
Responsibilities
Prepares content for presentations and multiple audiences, including assembling and organizing data into text and figures for presentations, publications, grant applications, reports, newsletters, and websites.
Edits and advises postdocs on writing scientific blog posts and articles for publication.
Develops and writes articles highlighting recent scientific publications by postdocs and faculty.
Researches and writes compelling articles and proposals that inspire philanthropy and disseminates research.
Fulfills other writing, copyediting, proofreading, and editorial duties as needed.
Collaborates with communications colleagues across the University to plan and implement communications that uphold University messaging, tone, style, and brand guidelines.
Researches, verifies, writes, and edits publications, which can include technical/scientific material for manuals or journals.
Uses knowledge of writing with moderate level of guidance to write in-depth pieces relating to specialized fields (e.g., scientific writing).
Performs other related work as needed.
Minimum Qualifications
Education:
Minimum requirements include a college or university degree in related field.
Work Experience:
Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.
Certifications:
---
Preferred Qualifications
Experience:
Writing news and feature stories for newspapers, magazines, or online outlets.
Editing the work of others, writers and non-writers.
Interviewing a wide range of subject matter experts, including academics and scientific researchers.
Familiarity with The Chicago Manual of Style.
Technical Skills or Knowledge:
Demonstrated skill and knowledge of Google Docs, Google Slides, Microsoft Word, Keynote, WordPress, Adobe Creative Suite, social media platforms, and other design and creative programs.
Familiarity with research and concepts in Artificial Intelligence and Machine Learning.
Preferred Competencies
Exceptionally strong writing skills; able to produce clear, compelling, and eloquent text.
Excellent editing and proofreading skills.
Ability to translate complicated scientific concepts for multiple audiences.
Keen understanding of creative content trends and best practices.
High attention to detail and follow-up, and excellent organizational skills.
Manage confidential information with discretion and tact.
Application Documents
Cover Letter (Required)
Resume (Required)
Writing Sample (Required)
When applying, the document(s) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.
Job Family
Communications
Role Impact
Individual Contributor
Scheduled Weekly Hours
37.5
Drug Test Required
No
Health Screen Required
No
Motor Vehicle Record Inquiry Required
No
Pay Rate Type
Salary
FLSA Status
Exempt
Pay Range
$65,000.00 - $75,000.00
The included pay rate or range represents the University's good faith estimate of the possible compensation offer for this role at the time of posting.
Benefits Eligible
Yes
The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the Benefits Guidebook.
Posting Statement
The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, shared ancestry, age, status as an individual with a disability, military or veteran status, genetic information, or other protected classes under the law. For additional information please see the University's Notice of Nondiscrimination.
Job seekers in need of a reasonable accommodation to complete the application process should call ************ or submit a request via Applicant Inquiry Form.
All offers of employment are contingent upon a background check that includes a review of conviction history. A conviction does not automatically preclude University employment. Rather, the University considers conviction information on a case-by-case basis and assesses the nature of the offense, the circumstances surrounding it, the proximity in time of the conviction, and its relevance to the position.
The University of Chicago's Annual Security & Fire Safety Report (Report) provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information. The Report can be accessed online at: *********************************** Paper copies of the Report are available, upon request, from the University of Chicago Police Department, 850 E. 61st Street, Chicago, IL 60637.
Auto-ApplyGrant Writer - Government Grants
Medical writer job in Countryside, IL
The Senior Grant Writer is an integral member of the Pillars Community Health Grants Management and External Affairs Teams. The Senior Grant Writer takes a lead role in the grant process including prospect research and recommendations, and preparation of new and renewal grant applications to federal, state, county, and local government grants. Under the direction of the Vice President of Grants/Community and Government Partnerships, the Senior Grant Writer works collaboratively with the staff across the organization in executing the strategy for government grant cultivation and management, and ongoing stewardship of existing and potential government funders.
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following.
* Assist program staff to support grant submissions to HRSA, SAMHSA, CDC for current federal grants and for new related grant submissions relevant to FQHC, CCBHC and Drug Free operations and expansion from agencies including HRSA, SAMHSA, CMS, state health departments, ICASA/ICADV, Cook County, Mental Health Boards/Commissions, and other government entities.
* Prepare and submit both new and renewal government grant proposals according to established requirements and deadlines.
* Serve as project manager for government grants as assigned, working with External Affairs, Finance and Program staff. Responsibilities include establishing and executing work plans for program planning, narrative preparation, budget preparation, and collection of supporting documents.
* Serve in a lead role for grant prospecting, identifying and researching prospects aligned with established organizational funding priorities and make recommendations for best grant opportunities.
* Upon notice of grant awards, work closely with Vice President of Grants/Community & Government Partnerships, Chief External Affairs Officer, External Affairs staff, Finance staff and program staff to create and execute plans for grant implementation. Implementation plans include establishing appropriate internal and external communication of awards, tracking tools, and methods of reporting of grant outcomes, both internally and in accordance with funder guidelines and requirements.
* Oversee portfolio of active government grants and ensure compliance with all federal, state, and local grant requirements and regulations, including 2 CFR 200 and OMB Circulars.
* Coordinates preparation with program staff to timely submit accurate and timely progress reports, financial reports, and other required deliverables to government agencies
* Navigate HRSA Electronic Handbooks (EHBs), SAMHSA SPARS, and other federal reporting systems to support program teams.
* Serve as primary liaison with government grant administrators and program officers.
* Shares grant writing expertise and provides guidance to supervisory staff or team members in the preparation of their government grant and reporting narratives.
* Utilizes expertise to suggest recommendations to improve workflows and procedures/processes.
* Assists with representing PCH in external meetings with government funders with VP or when the VP is unavailable.
* Assists VP with preparing for and/or leading Team meetings and/or assisting with Team projects, as needed.
* Work with External Affairs Team staff members to support consistent organization-wide messaging. Work collaboratively to maintain the library of current organizational program descriptions, measured outcomes, and demographics, including research data for use in government grants and other communication narratives.
* Keep abreast of funding trends, priorities, legislative and regulatory changes affecting government funding, and possible opportunities in line with established organizational funding priorities and strategic goals.
* Work with Vice President to cultivate and steward relationships with government funders and program officers through in-person, telephone, and e-mail contact.
* Write and submit periodic reports to funders according to established requirements and deadlines.
* Work closely with Vice President to maintain the organizational government grant calendar and project plans for submission of all new and renewal applications, reporting, and submission of supporting materials.
* Maintains grants master files and assures they are updated with new applications, awards and reports and other grants information.
* Maintain contact information and notes in Donor Perfect CRM and other systems as needed.
* Practice safety in the daily performance of job duties.
* Follows all organizational policies.
* Attend departmental and organizational meetings as required.
* Other duties as assigned.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and or ability required. Reasonable accommodations may be made to enable an individual with a disability to perform the essential duties and responsibilities.
EDUCATION AND EXPERIENCE
Bachelor's degree in Communications, English, Business, Public Health, or other related fields that would have provided coursework requiring structured written communication. Equivalent combination of education and experience may be considered in lieu of degree.
* 3-5 years of grant writing experience, preferably in healthcare or nonprofit sector
* Demonstrated experience with federal grants from HRSA, SAMHSA, or similar agencies, as well as state-level grants from ICASA/ICADV, Mental Health Boards/Commissions, or comparable entities
* Experience with FQHC and/or CCBHC operations strongly preferred
* Proven track record of successful government grant applications and compliance management
DEMONSTRATED COMPETENCIES
* Interest in working with staff throughout the organization to accurately portray programs and make a compelling case for support
* Knowledge of FQHC program requirements and HRSA funding mechanisms
* Familiarity with CCBHC criteria and behavioral health funding streams, including ICASA/ICADV violence prevention and intervention programs, and Mental Health Board/Commission funding priorities.
* Experience with HRSA EHBs, SAMHSA SPARS, or similar federal reporting systems preferred
* Ability to think strategically, set priorities and organize concurrent projects
* Ability to manage grant application processes, exercising independent judgment and assuming responsibility for reliable follow through.
* Mission mindedness, possessing a natural philanthropic "heart"
* Effective written communication skills to articulate program descriptions, details, outcomes and community impact to varied audiences.
* Excellent oral communication skills to interact with funders, team members, and program staff throughout the organization
* Excellent interpersonal, analytical and organizational skills
* Ability to multi-task and willingness to learn new tasks
* Computer proficiency in internet, email, and Microsoft Office, electronic donor database
* Experience with Donor Perfect and Microsoft Project is preferred
* Possess a high level of cultural humility and values diversity with the ability to work successfully with persons of all faiths, cultures, genders and socio-economic classes.
* Ability to work independently and as part of a team
PAY & BENEFIT INFORMATION
$57,000 - $65,000*
* Wage is based on one's experience and qualifications as compared with our position requirements and other similar employees within the organization.
Medical, dental, vision, short/long term disability, life, accident, critical illness, hospital indemnity, FSA, Employee Assistance Program, 401(k) retirement plan, paid time off for vacation, sick, personal time, holidays, & wellness day. Professional development membership to Relias Essential Learning.
Proposal Associate/Writer - Commercial Banking
Medical writer job in Chicago, IL
JobID: 210679822 JobSchedule: Full time JobShift: Day Base Pay/Salary: Chicago,IL $74,200.00-$99,000.00 Are you excited to be at the forefront of shaping the bank's strategic client relationships by working on complex proposals and delivering tailored solutions that drive business growth? You have found the right team!
As a Proposal Associate in the Commercial Banking Sales organization within the Commercial and Investment Bank, you will play a critical role in managing and writing responses to Requests for Proposals (RFPs) for treasury services, commercial card, and healthcare payment services. You will collaborate with sales and product teams to create client-focused, concise, compelling, and compliant proposals that strategically position J.P. Morgan.
The Proposal Team actively manages the process and writes proposals in response to RFPs for treasury services and commercial card products. This role begins working with the bank's proposal team members and other subject matter experts to write proposals in response to client/prospect RFPs. The Associate must independently manage projects from start to finish, ensuring that responses are complete, compliant and well positioned.
After successfully writing proposals this role has the opportunity to transition into actively managing proposals which includes working in a team environment, managing, writing, editing and proofreading responses to multi-product RFPs.
Job responsibilities
* Incorporate and revise pre-approved written responses as well as newly crafted responses into proposals
* Write custom, client-specific sections of the proposals Incorporate winning themes and features/benefits into the solution
* Ensure proper and consistent messaging by proofing, editing, and rewriting all sections of the document as required
* Identify any additional narrative needs and consult with subject matter experts to clarify details and develop custom responses
* Incorporate graphical elements materials and help identify any additional graphic needs and work with graphic artists to develop and finalize
* Translate and map technical information into language understood by all levels of clients
* Understand the client's RFP request and provide consultative advice to deal team
* Research topics, gather and analyze information and background materials
* Submit newly crafted sections to content management team to create new, re-usable proposal content
Required qualifications, capabilities, and skills
* A minimum of 3 years of sales, implementation or support of treasury management, commercial card or healthcare payment services
* A minimum of 2 years technical, business or proposal writing experience in banking/TS products.
* Excellent business writing and grammar skills are essential
* Intermediate to advanced Microsoft Word and Adobe Professional proficiency required
* Proven ability as a self-starter, detail oriented, well organized and able to multi-task effectively
* High level of independence, energy and integrity; demonstrates respect for a diversity of opinions and styles, and accepts accountability and responsibility
* Exceptional communication and interpersonal skills
* Ability to work effectively and efficiently as a team member on multiple projects with tight deadlines
* Schedule flexibility to meet deadlines with the ability to work flexible hours as required during critical phases of the project
* Ability to develop and maintain a broad knowledge of TS and Commercial Card products as well as the technology, equipment, operations processes and systems commonly used
* College degree (BA or BS) required
Preferred qualifications, capabilities, and skills
* Understanding of government bidding/ corporate procurement requirements and process
* Knowledge of TS, merchant, and/or commercial card products and services
Auto-ApplySenior Technical Writer
Medical writer job in Chicago, IL
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.
Easy ApplySr. Technical Writer
Medical writer job in Chicago, IL
At Early Warning, we've powered and protected the U.S. financial system for over thirty years with cutting-edge solutions like Zelle, Paze℠, and so much more. As a trusted name in payments, we partner with thousands of institutions to increase access to financial services and protect transactions for hundreds of millions of consumers and small businesses.
Positions located in Scottsdale, San Francisco, Chicago, or New York follow a hybrid work model to allow for a more collaborative working environment.
Candidates responding to this posting must independently possess the eligibility to work in the United States, for any employer, at the date of hire. This position is ineligible for employment Visa sponsorship.
Overall Purpose:
This position is responsible for planning, researching, and writing documentation that may comprise either or both of the following:
* Policies, Standards, Procedures and Work Instructions for internal business or technical processes.
* Technical content for products delivered to customers, including existing and new products.
* Responsible for managing assigned work projects, including determining deliverables, estimating effort, defining timelines, and reporting status.
* Responsibilities also include identifying process gaps as well as developing and improving content development and delivery standards and processes.
Essential Functions
* Meet with technical and business project stakeholders and subject matter experts to gather the information needed to create required internal and external documentation.
* Drive the process to determine the project scope and the document content that needs to be created and how it needs to be delivered (PDF documents, online (HTML), or other) to meet the needs of project stakeholders. May be required to work on several projects concurrently.
* Develop appropriate schedules and work plans for content development and manage the execution of those plans.
* Document status of project milestones for the Technical Writer workflow (Salesforce, Lockpath, ad other).
* Research and translate technical information / artifacts or business processes into content that can be delivered as output such as web content, online help, knowledge bases, technical requirements documents, system and implementation guides, reference manuals, user guides, training materials, policies and procedures, and associated forms.
* Track technical and non-technical changes and revise content, resolve issues, and verify the technical and functional accuracy of the documentation deliverables.
* Develop, apply, maintain, and continuously improve technical content development best practices and standards. This includes defining, implementing, and maintaining reuse model(s) for content single-sourcing.
* Maintain standard look and feel for content deliverables by formatting documents using defined CSS (styles), templates, and adhering to style guidelines defined by the Technical Writer Policies and Procedures.
* Create new or work with existing templates and CSS (styles and formats) to define standardized look and feel of documents. Experience using industry style guides (especially Google and Microsoft) and integrating into content development.
* Follow instructions to maintain version control of documentation defined by the Technical Writer Policies and Procedures. Identity and implement best practices for this activity.
* Create technical diagrams to depict system structure, program logic and process flow.
* Facilitate development of standard internal business processes across disparate teams.
* Identify/implement process gaps and define best practices for Technical Writing processes and standards. Also identify and implement efficiency and/or quality improvements for content development.
* Demonstrated competencies in communication, self-management / self-initiation, decision-making, and working cross-departmentally to proactively provide status and updates.
* Working knowledge of the enterprise business processes, systems and philosophy associated with high-performance technology companies.
* Support the company's commitment to protect the integrity and confidentiality of systems and data.
Minimum Qualifications:
* Bachelor's degree is preferred within a study of Technical Writing, Computer Science, Management Information Systems, English, Journalism, or a related field.
* Experience minimum of 8 years, dependent on the level and type of contribution, in defining and writing and editing technical manuals, guides and/or training aids or Policy, Standard and Procedure documentation.
* Intermediate to expert proficiency in Madcap Flare and its toolset.
* A passion and enthusiasm for technology and independent learning.
* Demonstrated experience managing large documentation projects to completion.
* Intermediate to expert ability in the use of graphics and publishing software, including Madcap Flare, MS Word, SnagIt, and Visio.
* Excellent verbal and written communication and collaboration skills.
* Ability to understand and effectively translate highly technical concepts and information into business and training materials.
* A strong desire for quality, attention to detail, and an ability to take ownership of assigned projects.
* Proven ability to work in a fast-paced environment, handling multiple priorities while meeting or exceeding deadlines.
* Skill to solve a wide range of complex problems related to creation and maintenance of documentation sets in creative and practical ways.
* Ability to understand and effectively translate highly technical concepts and information into business and training materials.
* Must have a strong desire for quality, attention to detail, and an ability to take ownership of assigned projects.
* Strong proficiency in software technology and a thorough understanding of technical writing.
* Fundamental knowledge of the business processes, systems and philosophy associated with high-performance technology companies.
* Background and drug screening
The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow instructions and perform other related duties as assigned by their supervisor.
Preferred Qualifications:
* Familiarity working within an Agile development methodology.
* Familiarity with software project management applications such as JIRA / Confluence and Microsoft Office 365.
* Intermediate to expert experience with content development applications and related software such as MadCap Flare, Adobe Acrobat Pro, Camtasia, SnagIt, Office 365 including Microsoft Word, Excel, SharePoint, Teams, Stream, and more.
* Proficiency with creating and / or maintaining CSS, HTML, JavaScript, and/or front end web development experience.
* Experience with API documentation, particularly REST API.
* Experience in documenting programming languages such as .net, objective C, and Java are a plus.
* Familiarity with document change management and source control using Git or similar.
* Additional related education and/or experience preferred.
Physical Requirements:
Working conditions consist of a normal office environment. Work is primarily sedentary and requires extensive use of a computer and involves sitting for periods of approximately four hours. Work may require occasional standing, walking, kneeling, and reaching. Must be able to lift 10 pounds occasionally and/or negligible amount of force frequently. Requires visual acuity and dexterity to view, prepare, and manipulate documents and office equipment including personal computers. Requires the ability to communicate with internal and/or external customers.
Employee must be able to perform essential functions and physical requirements of position with or without reasonable accommodation.
The base pay scale for this position in:
Phoenix, AZ/ Chicago, IL in USD per year is: $104,000 - $130,000.
New York, NY/ San Francisco, CA in USD per year is: $125,000 - $156,000.
Additionally, candidates are eligible for a discretionary incentive plan and benefits.
This pay scale is subject to change and is not necessarily reflective of actual compensation that may be earned, nor a promise of any specific pay for any specific candidate, which is always dependent on legitimate factors considered at the time of job offer. Early Warning Services takes into consideration a variety of factors when determining a competitive salary offer, including, but not limited to, the job scope, market rates and geographic location of a position, candidate's education, experience, training, and specialized skills or certification(s) in relation to the job requirements and compared with internal equity (peers). The business actively supports and reviews wage equity to ensure that pay decisions are not based on gender, race, national origin, or any other protected classes.
Some of the Ways We Prioritize Your Health and Happiness
* Healthcare Coverage - Competitive medical (PPO/HDHP), dental, and vision plans as well as company contributions to your Health Savings Account (HSA) or pre-tax savings through flexible spending accounts (FSA) for commuting, health & dependent care expenses.
* 401(k) Retirement Plan - Featuring a 100% Company Safe Harbor Match on your first 6% deferral immediately upon eligibility.
* Paid Time Off - Unlimited Time Off for Exempt (salaried) employees, as well as generous PTO for Non-Exempt (hourly) employees, plus 11 paid company holidays and a paid volunteer day.
* 12 weeks of Paid Parental Leave
* Maven Family Planning - provides support through your Parenting journey including egg freezing, fertility, adoption, surrogacy, pregnancy, postpartum, early pediatrics, and returning to work.
And SO much more! We continue to enhance our program, so be sure to check our Benefits page here for the latest. Our team can share more during the interview process!
Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records.
Early Warning Services, LLC ("Early Warning") considers for employment, hires, retains and promotes qualified candidates on the basis of ability, potential, and valid qualifications without regard to race, religious creed, religion, color, sex, sexual orientation, genetic information, gender, gender identity, gender expression, age, national origin, ancestry, citizenship, protected veteran or disability status or any factor prohibited by law, and as such affirms in policy and practice to support and promote equal employment opportunity and affirmative action, in accordance with all applicable federal, state, and municipal laws. The company also prohibits discrimination on other bases such as medical condition, marital status or any other factor that is irrelevant to the performance of our employees.
Auto-ApplySenior Proposal and Investment Writer
Medical writer job in Chicago, IL
Company: Heitman Founded in 1966, Heitman LLC is a global real estate investment management firm with over $36 billion in assets under management. Heitman's real estate investment strategies include direct investments in the equity or debt capitalization of a property or in the securities of listed and publicly traded real estate companies. Heitman serves a global client base with clients from North American, European, Middle Eastern and Asia-Pacific institutions, pension plans, foundations and corporations and individual investors. Headquartered in Chicago, with offices in Los Angeles, London, Luxembourg, Frankfurt, Munich, Warsaw, Hong Kong, Seoul, Tokyo, and Melbourne, Heitman's over 300 employees offer specialized expertise - from a specific discipline to local insight.
Job Description
Our Chicago office is seeking a Senior Proposal Writer who will develop responses to requests for proposals and due diligence questionnaires from consultants and prospective clients. This position will also handle updating the PMAPs content library, develop marketing collateral for the firm's funds and strategies, and will edit client communications, including quarterly and annual reports. The Senior Proposal Writer will work across Heitman's three complementary business units and will support the firm globally. This position will interact regularly with sales & client service, investment team members, and senior management. As the position will handle a high volume of work in a fast-paced environment, ideal candidates will exhibit strong attention to detail and the ability to effectively manage time and prioritize assignments.
Primary Duties -
May include, but not limited to the following:
RFPs
Write, organize, edit and format responses to requests for proposals (RFPs)
across all of Heitman's products and geographic regions
Analyze RFP requirements in order to write, answer, organize and edit proposal content
Coordinate sales and investment teams to establish RFP timelines and determine content ownership
Add new, update and maintain existing content within the firm's RFP database
Work with investment team members to develop and write new content
Ensure timely deliverable of quarterly updates, including documents in RFP library and updates to proposal database
Responsible for updating consultant databases on a regular basis
Provide feedback and recommendations to improve processes
Responsible for tracking, analysis and/or reporting on trends and RFP process effectiveness
Thought leadership development
Write, and coordinate development of various thought leadership pieces that can be leveraged across multiple platforms and present the firm's investment capabilities in the context of global secular and cyclical macroeconomic developments and client investment
challenges and objectives
Collaborate with resident experts and author articles to be published in target industry and other publications
Review and edit client communications, including quarterly and annual reports
Responsible for tracking, analysis and/or reporting on effectiveness
Qualifications
EDUCATION
Excellent academic qualifications; Bachelor's degree required. Degrees in Journalism, English, Political Science, Marketing or Communications preferred.
EXPERIENCE
7 years of direct job-related experience required
Financial services, real estate, or professional services industry experience a must
KNOWLEDGE, SKILLS, AND ABILITIES -
The following are essential:
Strong writing, editing, proofreading skills are essential
Direct experience leading, writing, editing and preparing RFPs
Direct experience leading, writing, editing and preparing thought leadership, content programs
Superior project management skills
Excellent interpersonal, verbal and written communication skills
High level of professionalism, client service skills and an enthusiastic team player
Ability to work efficiently and handle multiple projects in a fast-paced environment
Must be a results-oriented self-starter with strong attention to detail
Proficient in MS Office Suite (Word, Excel, PowerPoint), SharePoint
Experience working in PMAPS or Qvidian preferred
Additional Information
Interested professionals should apply via our website at **************** Please make sure to select “careers” under the About tab to submit your cover letter and resume.
If you are a Heitman employee, please make sure to apply using your Heitman email address.
NO PHONE CALLS PLEASE
Equal Employment Opportunity: Heitman is an equal employment opportunity employer and complies with all applicable laws prohibiting discrimination based on race, color, creed, religion, sex, age, national origin or ancestry, physical, medical or mental disability or condition (including, without limitation, HIV and AIDS), developmental disability, handicap, denial of family and medical care leave, denial of pregnancy leave, domestic partner status, status as a victim of sexual or domestic violence (or familial relationship to such victim), veteran status, marital status, sexual orientation, arrest records, citizenship status, criminal history that has been expunged, unfavorable discharge from the military, or any other basis protected by federal, state or local laws.
Specification/Label Editor I
Medical writer job in Lake Forest, IL
US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************
We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well.
Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset.
Job Description
Responsible for compliant change control of documentation and labeling including new and revised procedures, department SOPs, manufacturing specifications and domestic labeling artwork, outside contract and third party manufactured product. Responsibility includes day to day authority to develop, annotate, format, review and approve documentation and labeling. This position is responsible for the timely approval and release of specifications and labeling artwork in accordance with project milestones and customer requirements under the direct supervision of the section manager.
Receives general direction daily from specification/label editor.
Priorities and projects are assigned by the section manager.
Meet deadlines set by agencies
Perform activities related to creation of new and revisions to existing product labeling, manufacturing specifications, test methods, corporate procedures and department SOPs as well as abiding by change control processes to ensure that revisions made are in compliance with domestic regulatory regulations, business and customer expectations, and are properly justified and approved by accountable functional areas and are issued in a timely manner to support production schedules.
Resolve daily issues inherent to domestic product documentation and labeling.
Serve as the primary contact for day to day customer inquiries regarding domestic/international documentation and labeling change status, procedure and format.
Demonstrate financial fitness of documentation and labeling changes to minimize potential destruction by working with the plants and materials management on formulation of an implementation plan using best practices
Manage multiple assignments and meet all required timelines.
Demonstrate proficiency on SAP DMS Document Management System.
One to two years' experience in a technical, quality or operations area
Knowledge and familiarity with processing and testing of pharmaceutical products.
Knowledge of industry documentation, labeling and/or change control procedures.
Familiarity of graphics development and operations.
Plans, organizes and monitors workflow.
Prioritizes projects to ensure timely completion
Documentation and labeling control practices must be completed accurately, on time and per business, customer, and domestic agency regulations and requirements.
Quality of the product is directly linked to the accuracy of the documentation and labeling content.
Inaccurate documentation and labeling can delay product approval and launch or cause product quality issues in the field, potentially resulting in field actions and/or recalls.
Additional Information
Sneha
************
Grant Writer
Medical writer job in Hoffman Estates, IL
GiGi's Playhouse Inc.'s was founded in 2003 and our mission is to change the way the world views Down syndrome through national campaigns, educational programs, and by empowering individuals with Down syndrome, their families and the community. All Programs are free and are therapeutic in nature. Each program is designed to work on specific skill development, including speech and language, socialization and fine and gross motor skills. GiGi's Playhouse has 36 locations across North America and growing.
Job Description
GiGi's Playhouse, Inc. is seeking an experienced and enthusiastic grant writer to research and draft local, regional and national grants in support of Playhouse programs, marketing campaigns and capacity building. Some research and drafting efforts may also include helping other Playhouses with their grant, as well as collaboration on grants that leverage the national office for local support criteria. This is a part-time position that we envision to grow into a full-time role with 6-12 months.
This position requires excellent writing, communication and organizational skills, as well as attention to detail and the ability to prioritize and execute tasks in a deadline-oriented environment. The grant writer will work closely with the Development Director, Marketing Director, Founder and other GiGi's staff as needed.
Qualifications
The individual filling the grant writer role must, above all else, have an exceptional work ethic and the ability to confidently manage and optimize research and writing efforts. Additional skills and key strengths include:
· Demonstrated recent success in grant writing for non-governmental funding sources.
· Self-motivated and disciplined.
· Detail oriented and highly organized.
· Ability to work well under pressure.
· Strong research, analysis and reporting skills.
· Experience with online grant research databases.
· Experience with preparing project and proposal budgets.
· Skilled at synthesizing information and communicating it in a compelling and succinct form.
· Technology/computer savvy including familiarity with databases (Donor Perfect a plus).
Specific Accountabilities:
· Ensure all grant proposals represent and communicate GiGi's Playhouse mission and brand.
· Maintain ongoing grant pipeline; documenting all grants in Salesforce at various stages of lifecycle.
· Conduct foundation research, identify new funders and maintain a projected inform/award timeline.
· Define a list of grants to target and maintain timelines to ensure timely preparation and submission.
· Prepare all grant-related documents including letters of inquiry, program and project based cases for support, grant applications and proposals for support, and mid/post grant reports.
· Ensure all grant-related data is collected, summarized and shared with funders as needed, including mid-grant term progress and year-end reports.
· Fulfill additional grant-related writing projects (e.g. special correspondence with grantors, such as thank you letters and holiday cards).
· Support the GiGi's Playhouse network by providing grant templates, language and resources on shared server to ensure all are using the most current and effective grant language.
Additional Information
Competencies
Teamwork: Balances team and individual responsibilities; exhibits objectivity and openness to others' views; gives and welcomes feedback; contributes to building a positive team spirit; puts success of team above own interests; able to build morale and group commitments to goals and objectives; supports everyone's efforts to succeed.
Problem Solving: Identifies and resolves problems in a timely manner; gathers and analyzes information skillfully; develops alternative solutions; works well in group problem solving situations; uses reason even when dealing with emotional topics.
Written and oral communication: Ability to express ideas and thoughts verbally; expresses ideas and thoughts in written form; exhibits good listening and comprehension; keeps others adequately informed; selects and uses appropriate communication methods.
Adaptability: Adapts to changes in the work environment; manages competing demands; changes approach or method to best fit the situation; able to deal with frequent change, delays, or unexpected events.
Innovation: Displays original thinking and creativity; meets challenges with resourcefulness; generates suggestions for improving work; develops innovative approaches and ideas; presents ideas and information in a manner that gets others' attention.
Planning/Organizing: Prioritizes and plans work activities; uses time efficiently; plans for additional resources; sets goals and objectives; organizes or schedules other people and their tasks; develops realistic action plans.
Quality: Demonstrates accuracy and thoroughness; looks for ways to improve and promote quality; applies feedback to improve performance; monitors own work to ensure quality.
Customer Service: Manages difficult or emotional customer situations; responds promptly to customer needs; solicits customer feedback to improve service; responds to requests for service and assistance; meets commitments.
Technical Skills: Assesses own strengths and weaknesses; strives to continuously build knowledge and skills related to technical tools.
GiGi's Playhouse Core Values:
GiGi's challenges all staff and volunteers to embody the following core values:
Enthusiasm: Bringing positive, high energy to our work
Best of All: Always looking to improve in all that we do. Challenge yourself every day.
Get It Done: Making things happen and blasting through barriers when needed
Believe: Believe in ourselves, believe in our mission, believe we can achieve all that we set out to achieve
Locally Concerned, Enterprise Minded: Bringing our Best of All to our local playhouse while being mindful of how our work affects the broader GiGi's network.
Grant Writer
Medical writer job in Chicago, IL
Full-time Description About Enlace Chicago
Enlace Chicago convenes, organizes, and builds the capacity of stakeholders in Little Village to confront systemic inequities and barriers to economic and social access. Dedicated to creating lasting, community-driven change, Enlace fosters a safe and healthy environment, champions opportunities for educational advancement and economic mobility, and promotes social justice and systems change through collaboration and grassroots leadership. Our Education, Community Safety, Clinical Services, Community Health, and Immigration and Advocacy departments work collectively to strengthen the lives and opportunities of Little Village residents.
Position Overview
The Grant Writer plays a critical role in advancing Enlace Chicago's mission by securing and sustaining institutional funding from foundations, corporations, and government sources. This position is responsible for researching, developing, and writing compelling grant proposals and reports, ensuring compliance, and supporting donor stewardship. The Grant Writer collaborates across departments to translate program impact into persuasive narratives that reflect Enlace's values, strategy, and community-driven vision.
Key Responsibilities:
Grant Research and Strategy
Identify and evaluate new public and private funding opportunities aligned with Enlace's mission, strategic priorities, and community impact goals.
Maintain an updated grants calendar tracking proposal and reporting deadlines, renewals, and outcomes.
Support strategic planning for fund development and growth across departments.
Monitor trends in philanthropy and public funding to inform development strategies.
Proposal Development and Submission
Write, edit, and submit clear, persuasive, and tailored proposals and letters of inquiry.
Collaborate with program and finance teams to develop budgets, logic models, and data-driven narratives.
Translate complex program information into accessible, inspiring language that demonstrates outcomes and impact.
Ensure all submissions meet funder requirements and reflect Enlace's mission and tone.
Reporting and Stewardship
Draft, coordinate, and submit timely, accurate progress and final reports.
Support funder stewardship through thank-you letters, updates, and briefing materials.
Maintain meticulous records of all submissions, communications, and awards within the grants management system.
Partner with the Senior Vice President of Development to ensure compliance with all grant obligations and support organization-wide funding priorities.
Core Competencies
Exceptional Writing & Storytelling:
Translates data and program impact into compelling, human-centered narratives.
Project Management:
Balances multiple deadlines, priorities, and stakeholder needs with precision and accountability.
Strategic Collaboration:
Builds strong relationships with staff, funders, and partners to align funding strategies with program needs.
Analytical Thinking:
Synthesizes qualitative and quantitative data to craft persuasive proposals.
Attention to Detail:
Ensures accuracy, consistency, and quality in all writing and documentation.
Requirements
Bachelor's degree in English, Communications, Nonprofit Management, Public Policy, or a related field required; Master's preferred.
Minimum of 3-5 years of demonstrated success in grant writing or development within a nonprofit setting.
Proven track record of securing grants from foundations, corporations, or government sources.
Strong knowledge of program budgeting and outcome-based reporting.
Proficiency with Microsoft Office, Google Workspace, and donor databases (e.g., Salesforce, Foundant, or similar).
Excellent interpersonal and communication skills.
Ability to work both independently and collaboratively in a fast-paced environment.
Commitment to Enlace Chicago's values of social justice, equity, and community empowerment.
Bilingual (English/Spanish) strongly preferred.
Compensation: The salary range for this position annually is between $55,000 and $65,000. Salary is commensurate with experience in addition to the generous benefits package listed below.
Benefits:
Health benefits. Enlace Chicago offers you and your family access to a low-cost comprehensive health care plan, which includes medical (Bluecross Blue Shield), dental (Guardian), and vision (VSP) coverage.
Enlace Chicago also provides life insurance coverage and short-term and long-term disability insurance at no cost to you with options of additional coverage.
Retirement program. Enlace Chicago offers a voluntary 403(B) plan which begins at a 1% contribution. Enrollment is available after a 90-day grace period beginning on the first day of employment. An enrollment packet will be mailed to you.
Paid time off. You will receive 96 hours of Upon Hire hours, which will be prorated depending on your start date. After your 3rd month, you will accrue 3.33 hours per pay period or a total of 6.66 per month . All vacation days are considered above and beyond the approved holiday schedule. Enlace has 12 paid holidays with a Holiday week between Christmas and New Year's Day that will not be deducted from your PTO.
Our Commitment to Diversity, Equity, & Inclusion: At Enlace Chicago, we are deeply committed to fostering a diverse, equitable, and inclusive environment where all voices are heard and valued. We believe that diverse perspectives are essential to addressing the complex social challenges we seek to solve, and we strive to create a culture that promotes belonging, respect, and opportunity for all. Our mission is rooted in uplifting the stories of those who have been historically marginalized, and we actively work to ensure that our programs, partnerships, and workplace reflect these values. We welcome individuals from all backgrounds and encourage candidates who share our passion for social justice, equity, and inclusion to apply.
Enlace Chicago is an Equal Opportunity Employer. All applicants will be considered for employment without attention to race, color, sex, sexual orientation, gender identity, national origin, veteran or disability status.
Deadline for submission: Open until filled.
Salary Description 55K- 65K
Intern - Copywriting
Medical writer job in Chicago, IL
Hi there! We're Razorfish. We've been leading the marketing industry with our digital expertise since the start of the internet. But in 2020, we did a full reboot. What's different? It all starts with people. Weird, wonderful, complex people - with diverse backgrounds in strategy, creative and technology. But no matter how different we are, we all have one thing in common. We believe our differences are our strength. So we push for inclusion, challenge convention and bring in new perspectives, to inspire new ideas. Because when we connect by understanding what makes people different, we can create unforgettable experiences that enrich lives. Join us at razorfish.com.
Overview
Razorfish Summer Internship Program - 2026
Curious about what's next in marketing, technology, and creativity?
At Razorfish, we don't just follow trends-we help shape them. Our 2026 Summer Internship Program is designed for bold thinkers who want hands-on experience, meaningful collaboration, and exposure to real client work.
Applications are now open for college juniors, seniors, and recent graduates (up to six months post-graduation) who are eager to learn, contribute, and grow alongside industry leaders.
Program Details
Internship Dates: June 1 - July 31, 2026
In-Office: Hybrid (3 days per week in-office) - designed for collaboration, creativity, and connection
Office Locations: Chicago | Miami | New York | Birmingham, MI
Responsibilities
The wordsmith. The hashtag creator. Copywriters are the cunning linguists who write what you read, hear, and see. Also, the art director's partner in crime-professionally speaking, that is.
The Day-to-Day: Copywriters are responsible for writing copy on a variety of mediums; social media, blog posts, newsletters, brochures, product packaging, email marketing campaigns, etc. Prior to copywriting for a client, it is expected that copywriters research their subject matter, follow AP guidelines when writing copy, and develop their own tone of voice. Copy revisions are also a part of the copywriting process, so staying close to email/communication updates from their clients is crucial.
What You'll Experience
* Real Client Work: Gain hands-on real-world experience working with leading brands, and see your ideas move from concept to execution.
* Mentorship & Support: Learn from experienced teammates who provide guidance, feedback, and insight into agency life.
* A Culture That Values Your Voice: We encourage fresh perspectives and thoughtful ideas. You'll be invited to participate, share, and challenge our thinking.
* Professional Development: Build your skills through a guided campaign pitch competition, with access to industry-leading learning tools.
* Connection & Growth: Collaborate with cross-disciplinary teams and build relationships across the agency. High-performing interns may be considered for full-time opportunities, with continued growth supported through our early career development programs.
Qualifications
Who You Are
* A college junior, senior, or recent graduate (up to six months post-graduation)
* A student or recent graduate in Marketing, Advertising, Communications, Business, or a related field
* A strong communicator with an interest in storytelling, branding, and digital marketing
* Collaborative, adaptable, and comfortable working in a fast-paced, team-oriented environment
Additional information
At Publicis Groupe, we offer medical and voluntary benefits to our freelancers and temporary employees. Voluntary benefit options include supplemental medical insurance, transportation, and parking benefits, legal benefits, pet insurance, and auto and home insurance. You must be actively employed for 90 consecutive calendar days in order to be eligible for Publicis medical and voluntary benefits. You will also be eligible to participate in the Publicis 401(k) Plan after you complete 1,000 work hours in a consecutive 12-month period.
Razorfish is an Equal Opportunity Employer. Our employment decisions are made without regard to actual or perceived race, color, ethnicity, religion, creed, sex, sexual orientation, gender, gender identity, gender expression, pregnancy, childbirth and related medical conditions, national origin, ancestry, citizenship status, age, disability, medical condition as defined by applicable state law, genetic information, marital status, military service and veteran status, or any other characteristic protected by applicable federal, state or local laws and ordinances.
If you require accommodation or assistance with the application or onboarding process specifically, please contact *****************************.
All your information will be kept confidential according to EEO guidelines.
Compensation Range: $20/hr. This is the pay range the Company believes it will pay for this position at the time of this posting. Consistent with applicable law, compensation will be determined based on the skills, qualifications, and experience of the applicant along with the requirements of the position, and the Company reserves the right to modify this pay range at any time. Temporary roles may be eligible to participate in our freelancer/temporary employee medical plan through a third-party benefits administration system once certain criteria have been met. Temporary roles may also qualify for participation in our 401(k) plan after eligibility criteria have been met. For regular roles, the Company will offer medical coverage, dental, vision, disability, 401k, and paid time off. The Company anticipates the application deadline for this job posting will be April 1, 2026.
Grant Writer
Medical writer job in Chicago, IL
Summary: The Grant Writer is responsible for conducting the full range of grants management activities required to research, cultivate, prepare, submit, and manage grant proposals to foundation, government, and corporate sources.
Responsibilities
Solicits, prepares, and submits grant proposals and reports with support of program staff for BSCO.
Assists the Director of Resource Development in creating and implementing strategies to augment the organization's public, corporate, foundation and congregational donors.
Assists the Director of Resource Development to develop relationships with prospective institutional donors, including cultivation of immediate and long term prospects.
Co-leads site visits with prospect and current institutional donors.
Works with program staff to determine funding needs and help match program needs, both current and future, with potential funding sources.
Works with program directors to collect and report on previous and current year's outcomes and achievements.
Participates in prospect research activities on a regular and ongoing basis to identify new corporate, foundation, and public funding opportunities.
Ensures timely submission of grant proposals and reports.
Works with the Finance team to prepare the timely delivery of financial reports and related financial documents.
Develops systems to ensure compliance with all funder requirements, policies, and procedures.
Maintains electronic and hard files of all grant research, program background data, proposal submissions and funder communication using the organization's database and other tracking vehicles.
Maintains and updates calendar system to track grant deadlines, grant status, and communicates submissions, confirmations and declines to program staff and administration.
Contributes to the maintenance of agency database.
Perform other duties as assigned.
Copywriting & Content Strategy Internship
Medical writer job in Chicago, IL
What's This All About? Perfect Search offers a Copywriting & Content Strategy Internship that provides interns with experience in a strategic approach to copywriting and content within a digital marketing agency.
The internship includes responsibilities like search engine optimization (SEO) copywriting, blogging, ad copy creation, content strategy, and more.
At Perfect Search, we love our interns! In fact, many of our current employees began here as interns. This position is a great stepping stone for professional growth.
Duration of Internship: Flexible, 3 months preferred (timing TBD based on availability)
Availability: Flexible, 3 days preferred. Must be able to work in United States Central Time Zone Business Hours for training and meetings.
Must be eligible to work in the United States.
Available for college credit.
Applicants will be required to send a 1-3 page writing sample that displays their unique voice.
What You'll Learn
-Write and optimize a variety of content for clients (website content, blog posts, ad copy, etc.)
-Create content strategy plans with keyword research, user experience, conversion rate optimization, and SEO in mind
-Contribute to Perfect Search's internal content, including the blog and social media accounts
-Basics of PPC & SEO
-Collaboration between digital marketing and copywriting teams
-Work with fun people in a fun atmosphere
What You Need
-Excellent communication skills, both verbal and written
-Proficient in Microsoft Word, Excel, Google Sheets, Docs, and other reporting tools
-Background in Journalism, English, Communications, or a related field
-Knowledge of SEO a plus
Grant Writer (12-Month Retainer)
Medical writer job in Rolling Meadows, IL
Job Title: Contract Grant Writer (12-Month Retainer) Department: NeuroPoint Alliance (NPA) Reports To: Senior Manager, Outcomes Science FLSA Status: Part-time, retainer-based contract Contract Term: 12 months (with potential for renewal) Compensation: $40,000 total contract ($3,333.33 monthly retainer); 1099 contractor
Location: Remote (in-office appointments as needed)
About AANS, NPA, and NREF
The American Association of Neurological Surgeons (AANS) is a scientific and educational association with over 12,000 members worldwide, dedicated to advancing the specialty of neurological surgery and promoting the highest quality of patient care.
The NeuroPoint Alliance (NPA) serves neurosurgical and related practices, hospitals, industry, and patients through the collection, analysis, and reporting of clinical data. By leveraging high-quality data, NPA advances outcomes research, supports quality improvement, and drives evidence-based care.
The Neurosurgery Research & Education Foundation (NREF) supports research and education that advance the specialty of neurosurgery and improve patient care.
Together, NPA and NREF rely on philanthropic and grant support to expand their missions and impact.
Position Summary
AANS is seeking an experienced Contract Grant Writer to serve on a 12-month retainer to support both the NPA and NREF. This role will be responsible for identifying grant opportunities, drafting and submitting proposals, and assisting in the development of funding strategies to expand the organizations' impact.
The contractor will collaborate closely with AANS staff, leadership, and volunteer physician leaders to develop compelling cases for support and ensure compliance with grant requirements.
Key Responsibilities
Research and identify public and private funding opportunities aligned with NPA and NREF missions.
Develop high-quality, tailored grant proposals, letters of inquiry, and applications.
Maintain a calendar of grant deadlines, submissions, and reporting requirements.
Collaborate with staff and volunteer leadership to gather data, financials, and program information.
Prepare and submit required progress and final reports to funders.
Advise on grant strategies, donor trends, and long-term funding sustainability.
Provide monthly updates to AANS leadership regarding grant activity and progress.
Qualifications
Proven track record of securing grants from foundations, corporations, and/or government agencies.
Minimum of 5 years' professional grant writing experience, preferably in health care, medical research, or nonprofit organizations.
Strong research, writing, and editing skills with keen attention to detail.
Ability to translate complex scientific, educational, or policy concepts into clear, compelling narratives.
Knowledge of compliance requirements for federal and private grant funding.
Excellent organizational skills with the ability to manage multiple deadlines.
Experience working in a contract/consulting capacity preferred.
Application Process
Interested candidates should submit the following materials:
Resume/CV highlighting relevant grant writing experience
Cover letter outlining qualifications and approach to grant development
Two writing samples (preferably successful grant proposals or excerpts)
List of references
Working at AANS
AANS offers a mission-driven, collaborative environment focused on advancing neurological surgery. We provide competitive compensation, hybrid flexibility, generous benefits, and professional development opportunities.
Salary Description $40,000 annual contract ($3,333.33/month retainer)
Medical Writer
Medical writer job in Chicago, IL
Reporting directly to the Vice President of Clinical Development, the Medical Writer will be responsible for leading and executing all medical writing activities supporting Xeris' clinical programs. The individual will have a strong scientific background, exceptional writing skills, and a proven ability to translate complex clinical and scientific data into clear, accurate, and regulatory-compliant documents tailored to diverse audiences.
Responsibilities
Develop and author a broad range of clinical and regulatory documents, including but not limited to: clinical study protocols, investigator brochures (IBs), clinical study reports (CSRs), and sections of regulatory submissions (e.g., IND, NDA, etc.).
Ensure accuracy, clarity, consistency, and compliance with internal standards, applicable regulatory guidelines (e.g., ICH, FDA, EMA), and company SOPs.
Collaborate cross-functionally with colleagues in Clinical, Regulatory Affairs, Medical Affairs, and other internal stakeholders to gather relevant data and ensure consistency of messaging across documents.
Translate highly technical and statistical information into clear, concise content suitable for a wide variety of audiences including regulators, healthcare professionals, and non-scientific business leaders, as required.
Contribute to the development of communication materials, including slide decks, manuscripts, abstracts, and presentations, to support internal and external scientific communications.
Maintain document quality control through proofreading, editing, and adherence to templates, style guides, and version control procedures.
Manage timelines and priorities for multiple projects simultaneously, ensuring timely and accurate delivery of high-quality documents.
Provides detailed medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copy editing and content review.
Ensures document content and style adheres to FDA/EMA or other appropriate regulatory guidelines and complies with departmental SOPs and style guidelines.
Performs literature searches and reviews as necessary to obtain background information and provide literature references.
Provide input on processes, templates, and other business needs within the medical writing function.
Coordinate and/or manage review cycles to triage, incorporate, and resolve team comments, and lead discussion on document revision and finalization for both internally written and outsourced documents.
Serve as a point person for medical writing guidance and document-related problem resolution.
Qualifications
Bachelor's degree in Life Sciences or a related field is required; advanced degree (PhD, PharmD, or MS) strongly preferred.
Minimum of 5 years of medical writing experience in the pharmaceutical, biotechnology, or clinical research industry, with a focus on late-stage clinical development (Phase 3).
Demonstrated experience in writing regulatory submission documents in compliance with regulatory agency guidelines.
Proficiency in Microsoft Office Suite and familiarity with document management systems and version control tools.
Competencies: Attention to Detail, Organizational skills, Adaptability, Multi-Tasking, Strong Written & Verbal Communication skills, Independent Judgement, Cross-Team Collaboration, Critical Thinking, Problem Solving
Working Conditions: Position may require periodic evening and weekend work, as necessary to fulfill obligations. Periodic overnight travel.
This is a hybrid position located in Xeris' Chicago office and requires three days per week on-site. On-site requirement may change at management's discretion.
The level of the position will be determined based on the selected candidate's qualifications and experience.
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As an equal employment opportunity and affirmative action employer, Xeris Pharmaceuticals, Inc. does not discriminate on the basis of race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, veteran status, genetics or any other characteristic protected by law. It is our intention that all qualified applications are given equal opportunity and that selection decisions be based on job-related factors.
The anticipated base salary range for this position is $75,000 to $150,000. Final determination of base salary offered will depend on several factors relevant to the position, including but not limited to candidate skills, experience, education, market location, and business need. This role will include eligibility for bonus and equity. The total compensation package will also include additional elements such as multiple paid time off benefits, various health insurance options, retirement benefits and more. Details about these and other offerings will be provided at the time a conditional offer of employment is made. Candidates are always welcome to inquire about our compensation and benefits package during the interview process.
NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization.
Auto-ApplySenior Technical Writer
Medical writer job in Chicago, IL
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: *******************
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