Associate Director, Medical Writing - Lead Regulatory Docs
Rhythm Pharmaceuticals
Location: Boston, Massachusetts, United StatesCompany: Rhythm Pharmaceuticals Inc.Posted: 2026-08-03Rhythm Pharmaceuticals Inc. in Boston is seeking an experienced Associate Director of Medical Writing to independently author and oversee clinical, regulatory, medical, and safety documents across the development lifecycle.You will partner with cross-functional stakeholders to advance Rhythm’s mission of delivering precision medicines to patients with rare neuroendocrine diseases. The ideal candidate brings strong scientific judgment and regulatory writing expertise, plus the ability to lead#J-18808-Ljbffr
$154.4k - $242.55k
...and Precision Medicine The Global Regulatory Labeling Strategy Lead (Associate Director), Plasma-Derived Therapies... ...strategically interprets scientific, medical, and regulatory data and information... ...convey ideas verbally and in writing Innovation Disruptive thinker with...MedicalRegulatoryMinimum wageFull timeTemporary workLocal area- Merida Biosciences is seeking a Director, Medical Writing to lead development of clinical and regulatory documents supporting our advancing pipeline in a fast-paced biotech environment. Reporting to the Senior Director, Regulatory Affairs & Medical Writing, you will author...MedicalRegulatory
- Synterex, Inc. is seeking a senior medical writer to lead planning and preparation of high-quality regulatory documents within our medical writing team. You will partner across Clinical Development, Regulatory, and Program Management to deliver protocols, study reports,...MedicalRegulatoryRemote job
$142.73k - $237.88k
...Position Summary The Device Lead of Global MSAT Drug... ...post-approval regulatory change management, continued... ...820, (EU) 2017/745, Medical Device Regulation (MDR... ...93. Support Device Director, Device Strategy and Device... ...Awareness, Scientific Writing, Technology Transfer•...MedicalRegulatoryFull timeLocal area$100k - $186.3k
...experienced Senior Scientist/Associate Director to support and help lead operations of our state-... ...including other Harvard Medical School-affiliated... ...Support: Contribute to grant writing, progress reports, and... ...: Ensure adherence to regulatory, ethical, and institutional...MedicalRegulatoryFull time$120 - $170 per hour
Associate Director, Clinical Program Quality Leader Base pay... ...Unit (OBU) and Global Medical Marketed Products Development... ...are in place. Leads the clinical pre-... ...confirmed violations to regulatory authorities. Lead... ...problems. Strong technical writing skills; able to write...MedicalRegulatoryTemporary workFor contractorsWork at officeImmediate startNight shift2 days per week$167k - $286k
...to “Reimagine Possible”, we are leading the charge toward a world in which... ...of disease.Description: The Director/Associate Director, Platform and Pipeline Medical Affairs Lead will be responsible... ...discovery and developmentExperience writing and publishing clear, concise,...MedicalContract workTemporary workSummer workWork at officeLocal area$169.4k - $266.2k
...As part of the Global Medical Affairs Oncology team, you will report to the Director, Global Scientific Communications Group Lead. This is a hybrid role... ...stakeholder needsManage medical writing agency, including... ...analysesCompliance and Regulatory: Excellent...MedicalRegulatoryMinimum wageTemporary workFor contractorsFreelanceLocal areaRemote work- Job DescriptionGeneral Summary:The Associate Director, Medical Writing Science manages the overall operations... ...for document development for regulatory filings and coordinates the clinical... ...offerings also include inclusive market-leading benefits to meet our employees...MedicalRegulatoryFull timeWork experience placementSummer workWork at officeRemote workRelocation packageFlexible hours2 days per week3 days per week
$161.5k - $218.5k
...PharmaceuticalsPosted: 2026-08-16Overview The Associate Director, Medical Education Marketing, US Congress and TLL Asset Lead will lead national strategy and execution... ...to ensure all educational initiatives meet regulatory standards and strategic objectives.Performance...MedicalRegulatoryFull timeTemporary workLocal area- ...might include: Leading efforts of the... ...issues in regulatory agency meetings.... ...in professional associations, conferences, and... ...As an Associate Director, responsible for... ...Interact with Medical Directors, Clinical... ...Management, Medical Writing, and others to design...MedicalRegulatoryFull time
$172k - $237k
About This Role As the Associate Director for the Safety Surveillance... ...You’ll Do Serve as the lead PV Scientist for a... ...Clinical Development, Medical Affairs, Clinical Operations, and Regulatory colleagues.Respond to regulatory... ...safety reports writing in both clinical trial...MedicalRegulatoryFull timeTemporary workWork at officeLocal area$183k - $252k
About the RoleThe Global Associate Medical Director, Evidence Generation and Education... ...Disease Global Medical Lead and supporting the Global... ...Research, Value and Access, Regulatory, Patient Advocacy, Regional... ....Experience with technical writing and development of medical...MedicalRegulatoryFull timeTemporary workLocal areaWorldwide$185.37k - $308.95k
Associate Director, Medical Review Lead, MSRM Who we are At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive,... ...investigational and marketed products, ensuring medical accuracy, regulatory compliance, and high-quality safety data to support...MedicalRegulatoryTemporary workRemote workWork from homeFlexible hours3 days per week$148k - $222k
...SummaryThe Quality Systems Associate Director supports strategic... ...following:-Process Lead for Annual Product... ...with procedures and regulatory requirements Monitor... ...Excellent technical writing, presentation and communication... ...aspirations. From medical, dental and vision...MedicalRegulatoryFull timeSummer workLocal areaRemote workFlexible hours2 days per week$169.4k - $266.2k
About the Role The GMAO External Engagement Lead will be responsible for collaboratively... ...role supports Takeda Oncology’s global medical affairs objectives by driving impactful engagement... ...with Ethics & Compliance, Legal, and Regulatory to ensure compliant execution of all...MedicalRegulatoryMinimum wageTemporary workLocal area- Travere Therapeutics is looking for an Associate Director, Medical Writing who will oversee regulatory submissions and lead medical writing projects. The ideal candidate will have a Master's degree in Life Sciences, with at least six years of progressively responsible...MedicalRegulatoryRemote job
$133.5k - $192.83k
Job title: Associate Director, Field Learning & Development -... ...incorporate all appropriate regulatory and legal compliance... ...of the following: leading national training... ...both verbally and in writing.Ability to influence,... ...experience (Marketing, Sales, Medical, Compliance) strongly...MedicalRegulatoryFull timeTemporary work$160k - $240k
...seeking an experienced, highly motivated Associate Director of Medical Writing (MW) to independently author and oversee clinical, regulatory, medical, and safety documents across the... ...regulatory submissions, and response documents Lead medical writing activities for assigned...MedicalRegulatoryWork at office$92.5k - $124.25k
Ready to lead? Join ERM and help shape the future of sustainable... ...complex environmental and regulatory landscapes. In this role, you... ...transmission projects.Exceptional writing, communication, and strategic... ...time off, parental leave, medical, dental, vision, life, disability...MedicalRegulatoryFull timeFixed term contractCasual workWork at officeRemote workFlexible hours$122.25k - $176.58k
Job title: Lead, US Public Affairs & Patient Advocacy... ...societies, and associated institutions to build... ...including Corporate Affairs, Medical Affairs, Commercial,... ...Medical Affairs, Regulatory Affairs, Market Access... ...of strategy, analysis, writing, and decision-making rather...MedicalRegulatoryFull timeRemote work$105.8k - $175k
...Senior Environmental Permitting Lead to drive the successful... ...environmental permitting strategy, regulatory interface, and high-quality... .... Strong technical writing, editing, and communication skills... ...future. Employees have access to medical, dental, vision, and basic life...MedicalRegulatoryFull timeLocal areaRemote workShift work- Position Summary The Associate Director, Medical Writing provides strategic, operational, and people leadership for a team or major... ...of work within Medical Writing. This role leads the development of clinical and regulatory documents that support global regulatory filings...MedicalRegulatory
$175k - $190k
The Associate Director, Medical Writing provides strategic and operational leadership for medical writing activities... ..., fit‑for‑purpose clinical and regulatory documents aligned with program and... ...strategy, planning, and execution; leads clinical content development for complex...MedicalRegulatoryWork at officeLocal area3 days per week$237.2k - $372.79k
...shine? Join us as a Global Medical Lead, Dermatology in our Cambridge... ...brand team, market access, and regulatory strategies. This role leads... ...Expertise in study designs, writing protocols, analysis and... ...assess, and mitigate risks associated with clinical trials, regulatory...MedicalRegulatoryMinimum wageTemporary workWork at officeLocal areaRemote workWeekend work- ...LifeScience in the United States is seeking a Clinical Regulatory Writing Associate Director to lead complex regulatory writing across drug development... ...timely, compliant submissions. The role requires extensive medical writing experience in pharma or CROs, strong...MedicalRegulatory
$150k - $200k
A biopharmaceutical company is seeking a Medical Writing Lead to oversee the creation of clinical documents across drug development stages.... ...over 7 years of medical writing experience and expertise in regulatory submissions. This hybrid role allows employees to work from...MedicalRegulatory- Alnylam Pharmaceuticals is looking for a Senior Manager, Medical Writing to join our team in Cambridge, Massachusetts. This role involves... ...6 years of medical writing experience, familiarity with regulatory submissions, and excellent project management skills. A comprehensive...MedicalRegulatoryContract work
- ...an experienced Clinical Scientist, Associate Director to support oncology development efforts... ...strong data interpretation, medical writing, and regulatory submission capabilities, with occasional... ...business needs require. You will lead clinical data reviews, support medical...MedicalRegulatoryRemote job
- Agomab Therapeutics seeks a Senior Director of Medical Writing to anchor our hybrid medical writing model... ...will balance AI-enabled tools with regulatory rigor, partnering with Regulatory... ...ensure audit-ready submissions. You will lead CRO relationships, set standards,...MedicalRegulatoryRemote job
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