Senior Medical Writer, Regulatory CTD Lead (Remote)
Veristat
New York, NY
- Remote job
Veristat is seeking a Principal Medical Writer to independently plan and prepare regulatory documents and medical communications across product development. You will organize, analyze, interpret, and present scientific data per ICH guidelines and company standards, and collaborate with cross-functional internal and external teams. Ideal candidates have 7+ years in regulatory writing, a Bachelor's degree with MS or PhD preferred, and strong leadership to guide submission-level documents and #J-18808-Ljbffr Veristat
Vacancy posted 5 days ago
Similar jobs that could be interesting for youBased on the Senior Medical Writer, Regulatory CTD Lead (Remote) in New York, NY vacancy
- Syneos Health, Inc. seeks a Senior/Principal Medical Writer with a regulatory focus to lead and manage medical writing deliverables... ...timelines within budget. Remote work is available in the US, UK,... ...requires extensive experience with CTD modules, CSRs, IBs, and regulatory...Remote jobSeniorRegulatory
- ...inVentiv Health Commercial LLC is seeking a Sr Medical Writer Publications to lead the completion of medical writing deliverables remotely. This role involves managing writing activities, ensuring adherence to regulatory standards, and mentoring junior writers. The ideal...Remote workSeniorRegulatory
Syneos Health/ inVentiv Health Commercial LLC
United States2 days ago - ...inVentiv Health Commercial LLC is looking for a Sr Medical Writer Publications to manage and lead medical writing activities effectively. This remote role entails ensuring scientific accuracy in deliverables, adhering to regulatory standards, and coordinating efforts across...Remote workSeniorRegulatoryFlexible hours
Syneos Health/ inVentiv Health Commercial LLC
Hartford, CT1 day ago - Syneos Health is seeking a Senior Medical Writer Publications - Sponsor Dedicated - Remote Based to lead and manage medical writing deliverables across studies. You will ensure accuracy, maintain regulatory compliance, and mentor junior writers while coordinating with data...Remote jobSeniorRegulatory
- Synterex, Inc. is seeking a Senior Medical Writer to join their team remotely. This role involves leading the planning and preparation of clinical regulatory documents while collaborating with various departments. The ideal candidate has over 5 years of experience in medical...Remote jobSeniorRegulatory
- ...Health Commercial LLC is looking for a Sr Medical Writer Publications to lead the completion of medical writing deliverables. This remote-based role requires deep expertise in medical writing, ensuring compliance with regulatory standards, and mentoring less experienced...Remote jobSeniorRegulatoryFlexible hours
- ...Health/ inVentiv Health Commercial LLC is seeking a Sr Medical Writer Publications to lead medical writing deliverables and ensure clarity in scientific communication. This remote-based role involves adhering to regulatory standards, coordinating quality reviews, and...Remote jobSeniorRegulatoryFlexible hours
- Syneos Health/ inVentiv Health Commercial LLC is seeking a Senior Medical Writer to lead and manage medical writing deliverables. This remote-based role involves ensuring scientific clarity and adhering to regulatory standards in documents such as journal manuscripts and...Remote jobSeniorRegulatoryFlexible hours
- INC Research is seeking a Senior Medical Writer to support clinical study and regulatory project teams. This position is home based anywhere in the US. The ideal candidate will mentor junior writers while managing complex medical writing tasks across various therapeutic...Remote jobSeniorRegulatoryWork from home
- Syneos Health, Inc. is seeking a Senior Medical Writer (FSP) with proven experience in clinical document... ...and IBs. The role emphasizes meeting regulatory standards while delivering high-... ...documents on schedule. The position supports remote work with flexibility across EST/CST...Remote jobSeniorRegulatory
$126.9k - $215.4k
Your Role As the Senior Principal Medical Writer, you will lead the end-to-end development of complex regulatory submission documents—ensuring high communication... ...books, etc.). Solid CTD/CTD-like knowledge;... ...management. Vendor management and remote leadership. Strong...Remote workSeniorRegulatory- ## Job Details: Senior Manager, Medical/Regulatory WriterFull details of the... ...Medical/Regulatory Writer || | VN831 || | Full... ...Gaithersburg, MD, Radnor, PA, Remote, US || | Regulatory... ...be accountable for leading and overseeing the... ..., labelling, and CTD/BLA/MAA...Remote workSeniorRegulatoryFull timeContract work
- ...Scientific community. We are currently looking for a REMOTE Associate Director Medical Writer to work for a leading San Diego biotech company. Responsibilities... ...with Clinical Development, Biostatistics, and Regulatory teams to translate complex data into clear, high...Remote workSeniorRegulatoryWork at office
BioPhase
United States1 day ago - ...Leading the development and execution of medical writing strategies for clinical research projects, the full-time remote Senior Medical Writer will manage the preparation and editing of clinical study... ...skills Strong understanding of regulatory requirements for clinical...Remote workSeniorRegulatoryFull time
Virtual Vocations Inc
United States5 days ago - ...pharmaceutical, biotech, and medical device industries with a proven... ...to complex trial data and regulatory submission challenges. With a... ...minimal supervision, the Medical Writer will critically evaluate,... ...study protocol experience, as lead author, required Experience leading...Remote workSeniorRegulatoryWorldwide
MMS Holdings
United States5 days ago - ...collaborative individual for our medical writing team. Theseniormedical writer will partner cross-... ...,Biostatistics,Regulatory, and Program Management... ...underbrisktimelines. Location: Fully remote in the US, but must be... ...Responsibilities Lead theexecution of...Remote workSeniorRegulatoryLocal area
TransPerfect
Princeton, NJ2 days ago - ...professionals specializing in medical writing, submission... ...support.Synterexoffers remote or on-site services,... ...team.Theseniormedical writer will partner cross-functionallywith... ...,Biostatistics,Regulatory, and Program Management... ...Responsibilities Lead theexecution of...Remote workSeniorRegulatoryLocal area
Synterex Inc
Princeton, NJ1 day ago - ...Clinical Regulatory Document Specialist Company Overview Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons' most difficult challenges in...Remote workSeniorRegulatoryInterim roleWorldwide
Artivion
United States4 days ago - ...400670Reference26-00910Remote50% Remote Job Description Key Responsibilities · Lead FDA audit and inspection readiness... .../interface for FDA inspections, regulatory meetings, and compliance discussions... ...industries such as Pharma, Medical Devices, Biotechnology, or Healthcare...Remote workSeniorRegulatory
Katalyst Healthcares & Life Sciences
Bothell, WA2 days ago - ...Senior Medical Writer BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions. Guided by our purpose to develop... ...studies and reporting clinical study results for regulatory submissions and publications. Responsibilities:...Remote workSeniorRegulatoryFull timeFor contractorsShift work
BioMarin Pharmaceutical
United States1 day ago $115k - $185k
...A medical device company is seeking a Senior Regulatory Affairs Specialist to lead regulatory submissions and strategy for new product development. This role offers flexibility in levels and can be remote, aligned with US East Coast hours. Candidates should have a Bachelor...Remote workSeniorRegulatoryLexington Medical, Inc.
United States5 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 medical communications for reviewer-friendly clinical documents to support regulatory agency...Remote jobSeniorRegulatory
- MMS Holdings Inc is seeking an experienced Medical Writer based in Denver, Colorado. The role involves writing and editing clinical documents... ..., and mentoring team members. A strong background in regulatory writing and at least 3 years of experience in the pharmaceutical...Remote jobSeniorRegulatory
$145k - $155k
Terumo Group is seeking a Sr. Medical Writer for a remote role in Los Angeles. This position involves collaborating with clinical and regulatory teams to produce a range of medical documents for regulatory submissions, including clinical evaluation reports and study protocols...Remote jobSeniorRegulatory$55 - $75 per hour
A leader in biotechnology is seeking a Senior Medical Writer to draft and manage clinical documentation. This remote contract position offers a competitive hourly rate... ...writing skills, and a deep understanding of regulatory requirements. This role is crucial in supporting...Remote jobSeniorRegulatoryHourly payContract work$105k - $125k
...Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Senior Regulatory Medical Writer (FSP ; Remote; US ) At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale...Remote workSeniorRegulatoryTemporary workWork at officeLocal areaFlexible hoursThermo Fisher Scientific
United States1 day ago- MMS Holdings Inc is looking for a skilled Medical Writer to join their team in Atlanta, Georgia. The ideal candidate should have a minimum of 3-5 years of experience in regulatory writing within the pharmaceutical industry and possess strong writing capabilities. Responsibilities...Remote jobSeniorRegulatory
- ...inVentiv Health Commercial LLC in Idaho seeks an experienced medical writer to lead the completion of scientific deliverables for individual... ...minimal supervision. You will mentor junior writers, ensure regulatory compliance (ICH E3 and templates), manage budgets, and deliver...SeniorRegulatory
- 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
- Join MMS, an award-winning data-focused clinical research organization, as a Medical Writer. This full-time, UK-remote role focuses on producing regulatory medical writing deliverables with rigorous scientific standards. You will write and edit protocols, investigator...Remote jobSeniorRegulatoryFull time
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Medical Writer, Regulatory CTD Lead (Remote). Be the first to apply!
Related searches
- medical writer New York, NY
- senior medical writer New York, NY
- medical editor New York, NY
- medical writer remote New York, NY
- senior service associate New York, NY
- senior safety specialist New York, NY
- senior learning manager New York, NY
- senior vice president of business development New York, NY
- senior service designer New York, NY
- senior sales recruiter New York, NY