Senior Medical Writer — Regulatory CSR/Protocol Lead
$80.6k - $145kSyneos Health/ inVentiv Health Commercial LLC
A leading biopharmaceutical solutions organization in New Jersey is seeking a Senior Medical Writer to manage and complete regulatory documents. Responsibilities include writing clinical study protocols, ensuring adherence to regulatory standards, and mentoring junior writers. The ideal candidate will have over 5 years of experience in medical writing and excellent communication skills. This position offers competitive salary ranging from $80,600 to $145,000, along with a comprehensive benefits package including health insurance and flexible PTO. #J-18808-Ljbffr Syneos Health/ inVentiv Health Commercial LLC
Vacancy posted 5 days ago
Similar jobs that could be interesting for youBased on the Senior Medical Writer — Regulatory CSR/Protocol Lead in New York, NY vacancy
$80.6k - $145k
A leading biopharmaceutical solutions organization is seeking a Senior Medical Writer specialized in regulatory documents. In this role, you'll lead the preparation of clinical documents and manage writing activities while ensuring compliance with regulatory guidelines....SeniorRegulatory- A leading biopharmaceutical solutions organization in Georgia is seeking a Senior Medical Writer specializing in regulatory documents. The selected candidate will lead medical writing deliverables for clinical studies, ensuring compliance with regulatory standards and high...SeniorRegulatory
$80.6k - $145k
Senior Medical Writer - Regulatory Documents - CSR /Protocol - Late Phase Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into...SeniorRegulatoryContract workFlexible hours$80.6k - $145k
A leading biopharmaceutical solutions organization is seeking a Senior Medical Writer specializing in regulatory documents. This role involves managing medical writing activities, ensuring compliance with regulatory standards, and mentoring junior writers. The ideal candidate...SeniorRegulatory$119.3k - $159.3k
...BeiGene, Ltd. is seeking a Regulatory Writer to join its dynamic team in the United States. This role involves developing high-quality clinical and regulatory documents to ensure timely submissions of products. You will also mentor junior writers, ensuring compliance with...SeniorRegulatoryBeiGene
New York, NY3 days ago$101.8k - $152.6k
...Precision Medicine Group is seeking a Medical Writer to lead the development of high-quality clinical study documents. Responsibilities include... ...QC review of critical clinical documents compliant with regulatory guidelines (ICH, FDA). The candidate must have a BS degree...SeniorRegulatoryPrecision for Medicine
New York, NY1 day ago- Syneos Health/ inVentiv Health Commercial LLC is seeking an experienced medical writer in Georgia. The role involves leading medical writing projects, ensuring compliance with regulatory standards, and mentoring junior writers. You will create clinical documents and engage...SeniorRegulatoryFlexible hours
$80.6k - $145k
...Health/ inVentiv Health Commercial LLC in Kentucky is seeking a Medical Writer to lead clear and accurate medical writing projects. The successful... ...include completing clinical documents, adhering to regulatory standards, and mentoring junior writers. The position offers...SeniorRegulatoryContract workFlexible hours- ...Bristol Myers Squibb is looking for a Senior Scientific Writer I to author complex clinical... ...diverse disciplines, ensuring high-quality regulatory submissions. The ideal candidate will... ...documentation standards, and innovate in medical writing while adhering to regulatory...SeniorRegulatory
Bristol-Myers Squibb
New York, NY3 hours ago - ...Overview Senior Medical Writer (Remote) at MMS. Join to apply for the Senior... ...to complex trial data and regulatory submission challenges. With... ...but not limited to clinical protocols, investigator's brochures,... ...clinical study protocols as lead author. Experience leading...SeniorRegulatoryFull timeRemote work
MMS
New York, NY1 day ago $128k - $176k
...Senior Medical Writer Join us as we transform immunology and deliver medicines... ...to develop content for regulatory submissions that is well‑organized... ...content for phase 1‑4 protocols, master ICFs, IBs, and CSRs... ...writing activities. Supports the lead writer and project teams to...SeniorRegulatoryTemporary workargenx SE
New York, NY1 day ago$80.6k - $145k
Job Responsibilities Leads the clear and accurate completion of medical writing deliverables, ensuring... ...include clinical study protocols and clinical study... ...Adheres to established regulatory standards, including, but... ...experienced medical writers on complex projects, as...SeniorRegulatoryContract workFlexible hours$2,000 - $4,500 per month
...med-spa organization is seeking a Senior Legal Compliance and Licensing Specialist to lead compliance across multiple U.S.... ...over 5 years of experience in regulatory compliance within the med-spa or... ...coverage, and implementing operational protocols to maintain compliance. This...SeniorRegulatoryRemote workDermaVe Spa
New York, NY1 day ago$173.7k - $202.65k
...Cytokinetics, Inc. is seeking a Senior Manager, Regulatory Writing to oversee the development of regulatory... ...writing and editing clinical protocols, CSRs, and briefing materials while ensuring... ...be adept in project management and leading documentation efforts across teams. A...SeniorRegulatoryRemote workCytokinetics
New York, NY4 days ago$65k - $95k
...University of New York at Buffalo is looking for a Pulmonology Research Coordinator II to lead and oversee research programs. This role involves protocol development, regulatory compliance, and team supervision. Ideal candidates will have a Bachelor’s degree plus five...SeniorRegulatoryFull time- ...argenx SE is seeking a Senior Medical Writer to author and manage contributions for regulatory submissions, ensuring compliance with medical writing standards. The successful candidate will have a strong background in pharma or biotech, with at least 3 years of clinical...SeniorRegulatory
argenx SE
New York, NY4 days ago - ...Senior Lead Cybersecurity Architect Play a vital role in shaping the future of an iconic... ...standards and maintain compliance with regulatory requirements and internal policies.... ...standards: NIST, OWASP, MITRE, encryption protocols. Experience with multi-cloud strategies...SeniorRegulatory
Chase
Jersey City, NJ5 days ago - ...A leading biopharmaceutical company is looking for a Senior Medical Writer to develop clinical documents for regulatory submissions. The candidate will manage medical writing projects, lead timelines, and collaborate with cross-functional teams. Key qualifications include...SeniorRegulatoryRemote work
Itlearn360
New York, NY1 day ago - ...A leading biopharma company is seeking a Senior level Medical Writer to support clinical and regulatory writing projects. The role requires at least 8 years of medical writing experience in the biopharma industry and involves authoring key clinical documents, collaborating...SeniorRegulatoryContract workRemote work
Beacon Hill Inc
New York, NY6 days ago $136.5k
...Senior Director, Fraud Hub Lead At BNY, our culture allows us to run our company better and enables... ...standards that are adaptable to local regulatory requirements across functions. Oversee... .... Approve and oversee testing protocols to validate the effectiveness of fraud...SeniorRegulatoryTemporary workWork experience placementLocal areaWorldwideBNY
New York, NY1 day ago- ...A leading medical communications agency is seeking a Principal Medical Writer to lead scientific content development for various therapeutic areas. This fully remote role combines scientific leadership with mentorship, ensuring the quality of educational materials. Candidates...SeniorRemote work
Precision for Medicine
New York, NY1 day ago $95k - $105k
...A leading healthcare communications firm is seeking a Principal Medical Writer to develop high-quality medical content targeted toward healthcare professionals. The ideal candidate should have an advanced degree in a healthcare-related field and at least 3 years of experience...SeniorMJH Life Sciences, LLC
New York, NY1 day ago- ...A leading healthcare intelligence firm is seeking a Principal Medical Writer to lead the development of regulatory and clinical documents. The ideal candidate will have an advanced degree in life sciences and significant medical writing experience, particularly in regulatory...RegulatoryRemote workFlexible hours
ICON Strategic Solutions
New York, NY6 days ago - ...Senior Lead Cybersecurity Architect Join a team where you can play a crucial role in shaping... ...including MCP (Model Context Protocol) and post-quantum cryptography (PQC) for... ...resolutions Collaborate on audit and regulatory engagements, risk activities, and project...SeniorRegulatory
Chase
Jersey City, NJ5 days ago $80.6k - $145k
...Health/ inVentiv Health Commercial LLC is seeking a Medical Writer in Oklahoma. This role involves leading medical writing activities, ensuring the clarity... ...accuracy of various clinical documents, and adhering to regulatory standards. Candidates should have 3-5 years of...SeniorRegulatoryFlexible hours$80.6k - $145k
Syneos Health/ inVentiv Health Commercial LLC is seeking an experienced Medical Writer to ensure clear and accurate medical writing deliverables. The role demands 3-5 years of relevant experience, strong knowledge of FDA/ICH regulations, and a track record in the biopharmaceuticals...Senior- ...Senior Lead Architect Shape secure digital experiences and drive Customer Identity and... ...platforms, aligning with business goals and regulatory requirements. Designs, implements,... ...Deep knowledge of CIAM platforms, protocols (OAuth 2.0, OpenID Connect, SAML), and...SeniorRegulatory
Chase
Jersey City, NJ4 days ago $80.6k - $145k
...Health/ inVentiv Health Commercial LLC is looking for a Medical Writer in Delaware. The role involves leading medical writing deliverables, ensuring accuracy and... ...include writing clinical documents, adhering to regulatory standards, and mentoring junior writers. The...RegulatoryFlexible hours£190k - £200k per year
001 Brown & Brown, Inc is looking for an Associate Director as Employee Benefits Compliance Attorney to lead the Regulatory & Legislative Strategy team. This role involves developing strategies regarding health and welfare benefit regulations and collaborating across multiple...SeniorRegulatory001 Brown & Brown, Inc
New York, NY20 hours ago- ...Precision for Medicine is seeking a Senior Medical Writer responsible for developing high-quality clinical documents. The role involves planning, writing, and reviewing documents in compliance with regulatory guidelines. The ideal candidate will have a BS degree in a...SeniorRegulatory
Precision for Medicine
New York, NY4 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Medical Writer — Regulatory CSR/Protocol Lead. Be the first to apply!
Related searches
- medical editor New York, NY
- medical writer New York, NY
- freelance medical writer New York, NY
- medical writer remote New York, NY
- senior medical writer New York, NY
- freelance medical copywriter New York, NY
- senior game producer New York, NY
- senior manager process engineering New York, NY
- senior manufacturing engineer New York, NY
- senior director fp&a New York, NY