Remote Senior Medical Writer - Clinical & Regulatory Strategy
MSD Malaysia
New York, NY
- Remote job
Merck & Co., Inc. is seeking a seasoned Medical Writer to lead complex regulatory document development within the CRSC group, ensuring compliance with evolving guidelines. You will manage cross-functional teams of medical writers, review data for accuracy, and mentor junior staff while advancing publication quality and project timelines. This remote-friendly role offers a competitive salary, comprehensive benefits, and opportunities to influence regulatory content across development programs. #J-18808-Ljbffr MSD Malaysia
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Remote Senior Medical Writer - Clinical & Regulatory Strategy in New York, NY vacancy
- ...Inc. is seeking an experienced Clinical Operations leader to create... ...aligning resources with product strategy and ensuring timely delivery.... ..., budgeting, SOPs and regulatory compliance (FDA/ICH-GCP), build... ...travel as needed for trials; this remote role offers flexibility while...Remote jobSeniorRegulatory
- Alira Health is seeking a Senior Director of Clinical Operations to lead the company’s clinical development operations, manage cross-functional teams, and translate strategy into execution across regulatory, quality, and manufacturing functions. This role reports to the...Remote jobSeniorRegulatory
- ...Biostatistics to oversee statistical leadership in clinical trials and regulatory submission strategies. Your role includes collaborating with internal and... ...with regulatory authorities. The position supports remote work within the U.S. but involves travel to the corporate...Remote workSeniorRegulatory
- ...Therapeutics in San Diego, CA seeks an Associate Director, Clinical Pharmacology to design and lead pharmacology strategies across development programs, integrating PK/PD and DDI assessments to support dosing and regulatory submissions. You will partner with Research,...Remote jobSeniorRegulatory
- MMS Holdings Inc is seeking an experienced Medical Writer located in Bridgeport, Connecticut, to support... ...industries. The role involves writing clinical development documents and requires a strong background in regulatory writing alongside exceptional writing and organizational...Remote jobSeniorRegulatory
- MMS Holdings Inc is seeking an experienced Medical Writer based in Denver, Colorado. The role involves writing and editing clinical documents, evaluating medical literature,... ...mentoring team members. A strong background in regulatory writing and at least 3 years of experience...Remote jobSeniorRegulatory
- Stryker is hiring a Senior Staff Medical Writer for the Endoscopy Division, remotely anywhere in the United States. The role focuses on developing regulatory and clinical documentation to support global registrations and lifecycle management, partnering with Regulatory...Remote jobSeniorRegulatory
- ...based in Michigan, is seeking an experienced Medical Writer to take on critical analysis and writing responsibilities for clinical development documents. The ideal candidate will have 3-5 years of experience in regulatory writing and anticipate working closely with clients...Remote jobSeniorRegulatory
- 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. The...Remote jobSeniorRegulatory
- ...Rahway, NJ, USA seeks a Principal Medical Writer for the CRSC group to lead design,... ...-quality regulated documents with regulatory and health literacy compliance. You... ...improvements while applying deep clinical development knowledge. Remote work options available. #J-18808-...Remote workSeniorRegulatory
- MMS Holdings Inc in Austin, Texas seeks a skilled Medical Writer to evaluate medical literature and write essential clinical documents. Candidates should have 3-5 years of regulatory writing experience within the pharmaceutical industry. The Medical Writer is responsible...Remote jobSeniorRegulatory
- Stryker is hiring a Senior Staff Medical Writer for the Endoscopy Division. This role is based remotely within the United States, collaborating with Regulatory Affairs, Clinical Affairs, Quality, R&D, and Marketing to translate complex clinical data into regulatory and...Remote jobSeniorRegulatory
- MMS Holdings Inc is seeking a skilled Medical Writer in Chicago. The successful candidate will have a strong background in regulatory writing, including clinical protocols and study reports. They will ensure quality documentation while mentoring fellow team members and...Remote jobSeniorRegulatory
- MMS Holdings Inc in Baltimore, Maryland is seeking a Medical Writer to critically evaluate and write clinical documents for regulatory submissions. This role demands experience in the pharmaceutical industry and exceptional writing skills to produce high-quality documentation...Remote jobSeniorRegulatory
- ...Jersey City, NJ, is looking for an experienced Medical Writer to evaluate medical literature and produce essential clinical documents for pharmaceutical projects. The... ...candidate should have at least 3-5 years of regulatory writing experience, a degree in a relevant scientific...Remote jobSeniorRegulatory
- Merck & Co. seeks a skilled medical writer to prepare clinical regulatory and public-facing documents, ensuring regulatory compliance. You will lead cross-functional teams, apply lean writing and health literacy principles, and mentor junior writers to deliver high-quality...SeniorRegulatory
- Merck & Co. seeks a Clinical/Regulatory Medical Writer to develop and review regulated content across protocols, CSR, and public-facing documents, ensuring regulatory compliance and health-literacy standards. The role supports the CRSC within GCTO and partners with cross...SeniorRegulatory
- Jobtailor in New Jersey is seeking an experienced Medical Writer to prepare clinical regulatory documents and public-facing materials. You will design, plan, author, edit, and review high-quality documents, collaborating with cross-functional teams and mentoring junior...SeniorRegulatory
- Veristat, a global clinical research company, is seeking a Senior Medical Writer with a clinical focus to lead document authorship across service lines. The role... ...The qualified candidate will apply expertise in regulatory writing to support Clinical Study Reports, Investigator...Remote jobSeniorRegulatory
- ...development and execution of medical writing strategies for clinical research projects, the full-time Senior Medical Writer will manage the... ...the flexibility to work remotely or onsite. Key responsibilities... ...research, biostatistics, and regulatory affairs to analyze...Remote workSeniorRegulatoryFull time
Virtual Vocations Inc
United States1 day ago - ...issues today and address the medical challenges of tomorrow. We... .... Job Description The Senior Strategic Medical Writer is responsible for leading and writing clinical and regulatory documents for drug and/or... ...understanding of submission strategies. Coordinates the review, approval...Remote workSeniorRegulatoryTemporary work
Allergan
Brooklyn, NY2 days ago - SimulStat Inc. seeks a Sr. Medical Writer to support the development of global regulatory documentation strategy and the execution of tactics. You will conceptualize and develop... ...communications for reviewer-friendly clinical documents to support regulatory agency review...Remote jobSeniorRegulatory
$142k - $153k
Veristat in the United States is seeking a Principal Medical Writer to independently plan and prepare regulatory documents and medical communications across... ...working with cross-functional teams. This role offers remote work options, a competitive salary range of $142K-...Remote jobSeniorRegulatory- Syneos Health is seeking a principal medical writer to lead the development and review of complex regulatory and scientific documents, ensuring accuracy and alignment with client goals and regulatory guidelines. The role includes mentoring junior writers, coordinating cross...Remote jobSeniorRegulatory
$126.9k - $215.4k
Your Role As the Senior Principal Medical Writer, you will lead the end-... ...development of complex regulatory submission documents... ...define document strategy, shape submission timelines... ...stakeholders across clinical, regulatory affairs,... ...management and remote leadership. Strong...Remote workSeniorRegulatory- ...exciting opportunity for a Medical Writer ! Key Accountabilities : Author Clinical Documents Gather,... ...for submission to regulatory authorities, including... ...formalize a sound business strategy. Knowledge and... .... #LI-KW1 #LI-REMOTE...Remote workSeniorRegulatoryInterim roleFlexible hoursRemotea month ago
- ## Job Details: Senior Manager, Medical/Regulatory WriterFull details of the... ...Medical/Regulatory Writer || | VN831 || | Full... ...Gaithersburg, MD, Radnor, PA, Remote, US || | Regulatory... ..., PV, preclinical, clinical, translational... ...messaging strategy in collaboration with...Remote workSeniorRegulatoryFull timeContract work
$90k - $100k
...Position Summary The Senior Medical Writer serves as an... ...compelling and relevant clinical communications and commercial... ...of scientific strategies and tactics. This is... ...Lambertville (NJ)—or remotely within the US,... ...client medical/legal/regulatory reviews by highlighting...Remote workSeniorRegulatoryWork experience placementCasual workWork at officeNight shiftWeekend work2 days per week$110.1k - $183.4k
...Stryker is hiring a Senior Staff Medical Writer to join our... ...Division, to be based remotely anywhere within the... ...develop scientific and clinical documentation that supports global regulatory compliance and market... ...develop clinical evidence strategies, regulatory...Remote workSeniorRegulatoryFull timeTemporary workFlexible hoursStryker
Portland, OR24 days ago- ...Leading data management activities for clinical studies, the full-time remote Senior Clinical Data Manager will oversee... ...processes, data management, and regulatory obligations within the CRO... ...Proven leadership skills in project strategy and team motivation Ability to mentor...Remote workSeniorRegulatoryFull time
Virtual Vocations Inc
United States27 minutes ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Remote Senior Medical Writer - Clinical & Regulatory Strategy. Be the first to apply!
Related searches
- medical editor New York, NY
- freelance medical copywriter New York, NY
- medical writer remote New York, NY
- freelance medical writer New York, NY
- medical writer New York, NY
- senior medical writer New York, NY
- junior remote developer New York, NY
- college summer internship remote New York, NY
- remote senior salesforce administrator New York, NY
- remote transcription New York, NY