Scientific Writer
Harvard Central Administration (CADM) Talent Acquisition
Overview Company Description: By working at Harvard University, you join a vibrant community that advances Harvard's world-changing mission in meaningful ways, inspires innovation and collaboration, and builds skills and expertise. We are dedicated to creating a diverse and welcoming environment where everyone can thrive. Why join Harvard University Central Administration? Harvard University's Central Administration (CADM) is a 5,000+ employee organization that supports the university's overall excellence by understanding and serving the needs of its schools, students, faculty, staff, alumni, and surrounding communities. Through dynamic and collaborative partnerships, CADM provides high-quality and efficient services to the schools to help them achieve their goals. Job Description JOB RESPONSIBILITIES The Harvard Global Health Institute (HGHI) serves as the connective tissue for global health across all 15 Harvard schools. As a university-wide hub, we convene and facilitate collaboration between world-class faculty, students, and global partners to ensure that expertise in multiple disciplines aligns to advance health equity worldwide. Our work is grounded in the belief that we must inform each other\'s work to transform health at every level. HGHI seeks a Scientific Writer to support the institute’s scholarly and research mission. Reporting to the Executive Director and working in collaboration with HGHI’s Faculty Director and, at times, affiliated faculty, this role is responsible for the production of high-quality institutional scholarly products, including grant proposals, technical policy briefs, research reports, and working group publications. This is an institute-level position supporting HGHI’s collective research and programmatic activities. This role requires the ability to navigate both technical and public-facing writing, ensuring that institute outputs meet rigorous academic standards while remaining accessible to diverse stakeholders, including funders, policy makers and, at times, the broader public. Primary responsibilities include: Serve as writing lead for academic outputs, grant proposals, reports, policy briefs as assigned by Executive Director in collaboration with Faculty Director. Research, draft, edit, and produce technical policy briefs on global health topics for the institute, funders, and public. Search literature, compile literature reviews, synthesize complex research evidence into clear, policy-relevant documents that support HGHI’s mission. Revise scientific manuscripts, research papers, and reports for technical and specialist audiences. Ensure accuracy, rigor, and appropriate citation of sources across all institutional publications, adhering to institutional guidelines and publication standards. Scientific Editing and Quality Assurance Provide technical review and editing of public facing communications materials (press releases, newsletters, website content, and social media) produced by the Communications team to ensure scientific accuracy. Maintain consistency in tone, style, and formatting across HGHI’s scholarly and institutional publications. Stay current on trends in scientific communication, publication standards, and ethical and responsible use of AI-assisted writing tools, integrating best practices into HGHI’s writing and editing workflow. Grant Writing and Institutional Proposals Draft, edit and manage the production of grant proposals and funding applications on behalf of HGHI to external funders including foundations, government agencies, and multilateral organizations. Collaborate with the Faculty Director, Executive Director and, when assigned, affiliated faculty to translate research concepts into compelling, well-structured proposals that meet funder requirements. Prepare ancillary proposal materials including budget narratives, letters of support, bio sketches, and compliance documentation in coordination with the Finance Team. Cross-Institutional Coordination Coordinate with internal teams and external collaborators, including partner institutions, co-investigators and journal editors to produce cohesive, polished content for joint projects and publications. Prepare and organize ancillary materials, figures, appendices, graphs, copyright permissions, and other materials to submit to publication platforms, as necessary. Qualifications Basic Qualifications are the minimum threshold a candidate must meet in order to be considered for this role. Five or more years of professional experience in scientific or technical writing, with demonstrated experience writing grant proposals, research reports and technical policy documents. Additional Qualifications and Skills: Master’s Degree (MA, MS, MPH or equivalent) in public health, global health, or a related field. PhD or doctoral degree in a relevant field preferred; equivalent professional experience in grant writing and scientific publishing will be considered. Subject matter expertise in global health, public health, including familiarity with major funders, research frameworks, and policy processes in these fields. Experience writing successful grant proposals for foundations and government agencies. Experience managing or leading writing projects with diverse stakeholders in academic or research institutions. Proficiency in project management tools (e.g., Asana), Microsoft Office Suite, and citation management software (e.g., Zotero, RefWorks, Sciwheel). Familiarity with AI-assisted research and writing tools, with an understanding of their responsible application in scholarly contexts. Additional Information Standard Hours/Schedule: 35 hours per week Visa Sponsorship: Harvard University is unable to provide visa sponsorship for this position Pre-Employment Screening: Harvard University requires pre-employment reference and background screenings: Identity Other Information: Requirements: Two writing samples demonstrating range across technical/scholarly and accessible/public-facing writing (e.g., a grant proposal excerpt, a policy brief or published article). List of publications or representative writing portfolio. This position will have a 3-month orientation and review period. Work Format Details This position has been determined by school or unit leaders that some of the duties and responsibilities can be effectively performed at a non-Harvard location. The work schedule and location will be set by the department at its discretion and based upon operational needs. When not working at a Harvard or Harvard-designated location, employees in hybrid positions must work in a Harvard registered state in compliance with the University’s Policy on Employment Outside of Massachusetts. Additional details will be discussed during the interview process. Certain visa types and funding sources may limit work location. Individuals must meet work location sponsorship requirements prior to employment. Salary Grade and Ranges This position is salary grade level 056. Please visit Harvard\'s Salary Ranges to view the corresponding salary range and related information. Benefits Harvard offers a comprehensive benefits package that is designed to support a healthy work-life balance and your physical, mental and financial wellbeing. Because here, you are what matters. Our benefits include, but are not limited to: Generous paid time off including parental leave Medical, dental, and vision health insurance coverage starting on day one Retirement plans with university contributions Wellbeing and mental health resources Support for families and caregivers Professional development opportunities including tuition assistance and reimbursement Commuter benefits, discounts and campus perks Learn more about these and additional benefits on our Benefits & Wellbeing Page. EEO/Non-Discrimination Commitment Harvard University is committed to equal opportunity and non-discrimination. We seek talent from all parts of society and the world, and we strive to ensure everyone at Harvard thrives. Our differences help our community advance Harvard\'s academic purposes. Harvard has an equal employment opportunity policy that outlines our commitment to prohibiting discrimination on the basis of race, ethnicity, color, national origin, sex, sexual orientation, gender identity, veteran status, religion, disability, or any other characteristic protected by law. Harvard\'s equal employment opportunity policy and non-discrimination policy help all community members participate fully in work and campus life free from harassment and discrimination. #J-18808-Ljbffr
- ...and global partners to ensure that expertise in multiple disciplines aligns to advance health equity worldwide. HGHI seeks a Scientific Writer to support the institute’s scholarly and research mission. Reporting to the Executive Director and working in collaboration with...SuggestedWork at officeWorldwide
$90k - $100k
...as project and client management, to join us as Senior Medical Writers in our Medical Communications team. In this role, you will be... ...clients, supervising the project team, and producing high-quality scientific content themselves. They ensure projects are delivered to an...SuggestedPermanent employmentFull timeTemporary workWork at officeImmediate startWork from homeFlexible hours- ...pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission... ...Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature...SuggestedRemote workWorldwide
$105k
...Affairs SOPs. Performs other non-routine duties as assigned. Required Knowledge, Skills and Abilities Bachelors Degree in a relevant scientific discipline, or equivalent combination of education and experience. A minimum of 3 years medical writing experience. Direct...SuggestedTemporary workFixed term contractWork at officeRemote workWorldwideFlexible hours$150k - $190k
...Senior Medical WriterThe Senior Medical Writer will be responsible for authoring and managing clinical regulatory documents in support... ...document standards.QualificationsPhD or advanced degree in a scientific or clinical discipline.4+ years of medical writing or relevant...SuggestedFull time- ...Medical Writer In this role, incumbent will be expected to provide Medical Writing leadership for clinical development, registrational... ...: must be a strong technical leader, manage with excellent scientific, strategic and customer focused leadership. Partner with Clinical...Contract work
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...together. Opportunity Overview As a Senior Medical Communications Writer, you will be responsible for researching, writing, and editing... ...provide writing support for associated materials to the Global Scientific Communications department. Responsibilities and Duties Perform...FreelanceWork at office$95k - $125k
...collaborative, high-performing team known for delivering best-in-class scientific communications and maintaining long-standing client... ...standards, and key statistical concepts You are an exceptional writer, able to translate complex data into clear, compelling, and accurate...Local area$172k - $232.8k
...Principal Medical WriterThe Principal Medical Writer (equivalent to Associate Director) represents medical writing on multi-disciplinary... ...informed consent forms, health authority briefing books, and scientific publications.Independently lead supplemental filings, Type 2...Contract workFor contractors$71.25k - $101.78k
...Payfuture Technologies is seeking a Medical Writer for DynaMedex. This remote/hybrid role requires strong writing skills for medical content and collaboration with experienced colleagues. A Bachelor’s degree and relevant experience are essential for success in summarizing...Remote work- ...the Role Synterex is seeking an organized, motivated, and collaborative individual for our medical writing team. The senior medical writer will partner cross-functionally with client teams in Clinical Development, Clinical Operations, Biostatistics, Regulatory, and...Local areaRemote work
- ...Medical Writer Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional... .../oversee SRLs/FAQs development processes. Includes researching scientific literature and internal research documents and data feeding the...Work at office
- The Massachusetts General Hospital Down Syndrome Program (MGH DSP) seeks a Scientific Writer to draft, edit, and refine manuscripts, grant proposals, and educational materials that clearly communicate Down syndrome research to medical professionals, patients, families,...
$95k - $125k
...their team dedicated to improving patient outcomes through impactful communications. This role involves developing high-quality scientific content and collaborating closely with cross-functional teams to deliver client-ready materials across various therapeutic areas....$71k - $76.5k
...This role is available in our Boston office. About the Role The Analyst and Medical Writer positions are ideal for recent graduates in the sciences, and those with experience in scientific research, who are seeking the opportunity to apply their knowledge to real‑world...Permanent employmentFull timeWork at officeWork from homeFlexible hours$71k - $76.5k
...is available in our Boston office About the Role The Analyst and Medical Writer positions are ideal for recent graduates in the sciences, and those with experience in scientific research, who are seeking the opportunity to apply their knowledge to real-world...Permanent employmentFull timeTemporary workWork at officeImmediate startRemote workWork from homeWorldwideFlexible hours$70k - $98k
...content and presentation outline. Collaborates with authors and account management team on content revisions and works with clinical writers, account teams, production, and other staff to increase ease of project completion. Represent department at internal start up and...Work at officeFlexible hours- [Voronoi, Inc.] Medical Writer (Hybrid Work) Medical Writer - Oncology Clinical Trials Location: minimum 2 days onsite in Waltham, MA... ...a proven track record of preparing high-quality regulatory and scientific documents in support of clinical development programs. Key...For contractors
$100k - $120k
...on programs to meet strategic objectives Work closely with the Associate Medical Director in managing multiple accounts from a scientific perspective including all scientific and strategic aspects of medical communication tactics, meetings, and programs Participate...InternshipLocal areaRemote workFlexible hours- Principal / Senior Medical Writer - with proven strong clinical document writing experience Updated: Yesterday Location: Remote, NH,... ...accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately. Manages medical...Contract workRemote work
- A clinical-stage biotechnology company is seeking a Medical Writer to lead the development of regulatory and clinical documents. The role requires expertise in medical writing and collaboration with various teams to ensure high-quality documentation. Candidates should...
- MMS Holdings Inc in Boston is seeking a Medical Writer to evaluate medical literature and prepare clinical documents, including clinical protocols and study reports. This role requires at least 3-5 years of regulatory writing experience in the pharmaceutical industry....Remote job
$150k - $180k
...centralized infrastructure. Description of Role The Senior Medical Writer will author and manage clinical regulatory documents in support... .... Qualifications Advanced degree: PhD, PharmD, Master’s in a scientific/clinical field or English. 4+ years of medical writing or...Full time- The Principal Medical Writer represents medical writing on multi-disciplinary teams, collaborates on the development of clinical documents in accordance with all applicable regulations, Good Clinical Practices, and Standard Operating Procedures (SOPs), and oversees the...Contract work
- Voronoi, Inc. is seeking an experienced Medical Writer with a strong background in oncology clinical trials. This hybrid role requires... ...in Waltham, MA / Cambridge area, supporting regulatory and scientific documents for oncology programs. The candidate will write, edit...
$80k - $100k
...opportunity for an outstanding individual to join a rapidly growing digital health company as a Medical Policy Writer. You will work closely with scientific literature researchers, clinical leadership, subject matter experts, and stakeholders to ensure the smooth flow...Remote workFlexible hours$21 - $46 per hour
Dart Solutions is looking for an intern for its Medical Writing Operations team based in Boston. This role involves supporting the finalization activities of clinical documents by performing detailed QC checks, edits, and ensuring compliance with regulatory standards. Ideal...Remote jobHourly payInternship- ...Job Description Job Description Job Title: Scientific Writer (Onsite Consultant)Location: Cambridge, MAAbout the Role:We are seeking an experienced Scientific Writer with a strong background in scientific editing and publication to support our research and communications...
- MMS is an innovative CRO focused on regulatory-grade trial data and submissions. The Medical Writer will evaluate literature, draft protocols, summaries, and regulatory documents with expert accuracy under timelines. Ideal candidates have 3+ years in pharma regulatory...
- Alnylam Pharmaceuticals in Cambridge, MA, is seeking a Principal Medical Writer (equivalent to Associate Director) to lead medical writing on multi-disciplinary teams and oversee contract writers on the clinical program. You will develop key clinical documents in accordance...Contract work
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