Senior Medical Writer: Regulatory Submissions (Remote)
Veristat
- Remote job
Veristat is seeking a Principal Medical Writer to play a crucial role in planning and preparing regulatory documents to support product development. This position allows for a flexible, inclusive culture with 70% remote workforce. The ideal candidate will have a Bachelor’s degree, 7+ years of medical writing experience, and strong expertise in regulatory guidelines. Key benefits include flexible time off, medical insurance, and tuition reimbursement. #J-18808-Ljbffr Veristat
$116k - $128k
Veristat, LLC. is looking for a Senior Medical Writer with a clinical focus, responsible for leading... ...role demands a strong background in regulatory writing and clinical documentation, with... ...$116K to $128K and provides a fully remote working option. Benefits include flexible...Remote jobSeniorRegulatoryFlexible hours- A leading data-focused CRO is seeking a Remote Senior Medical Writer to contribute to clinical development documents and mentor team members. Candidates should have strong writing skills, at least three years of experience in the pharmaceutical industry, and an educational...Remote jobSeniorRegulatoryFull time
- ...organization in the United States, seeks a Senior Medical Writer – Clinical Focus to lead document... ...of a delivery team. You will guide regulatory documentation, ensure adherence to guidelines... ...and contribute to the development of submission documents such as CSRs, IMs, and...Remote workSeniorRegulatory
- ...Medical Writer MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries... ...with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents...Remote workSeniorRegulatoryWorldwide
- ...Rodenberg, PhD is hiring a Senior Medical Writer! What stands out most to me working with the Regulatory and Clinical Affairs leadership... ..., but we are also open to remote applicants. The Senior Medical... ...reviews, and regulatory submissions. Plan and report clinical data...Remote workSeniorRegulatoryWork at officeLocal area
$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- ...Senior Medical Writer Company Overview Headquartered in suburban Atlanta, Georgia, Artivion,... ...standards as applicable Writing clinical regulatory documents including annual reports,... ...clinical requirements for regulatory submissions and maintenance. Coordinating company...Remote workSeniorRegulatoryInterim roleWorldwide
- MMS Holdings Inc in Boston is seeking a Medical Writer to evaluate medical literature and... ...This role requires at least 3-5 years of regulatory writing experience in the... ...team members and ensuring high-quality submissions to regulatory authorities. #J-18808-Ljbffr...Remote jobSeniorRegulatory
- ...deep domain expertise in regulatory sciences, clinical... ...compliance, pharmacovigilance, medical information, and R&D... ..., NDA, BLA, MAA, eCTD submission‑level documents).... ...experienced medical writers, as necessary. Adheres... ...While ProPharma supports remote working, we also...Remote workSeniorRegulatoryContract workWork at office
- Sr. Principal Regulatory Medical Writer - Oncology (Preferred) at Syneos Health/ inVentiv Health Commercial LLC is responsible for authoring regulatory documents for global submissions in line with ICH guidelines and internal standards. The role requires steering timelines...SeniorRegulatory
- ...inVentiv Health Commercial LLC is seeking a Sr. Principal Regulatory Medical Writer with expertise in oncology. The role involves developing regulatory... ...with cross-functional teams to ensure successful submissions. Responsibilities include creating Clinical Study Reports...SeniorRegulatory
- ...Senior Medical Writer BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions. Guided by... ...clinical studies and reporting clinical study results for regulatory submissions and publications. Responsibilities: Drafts and...Remote workSeniorRegulatoryFull timeFor contractorsShift work
- 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... ...in supporting clinical research and regulatory submissions. #J-18808-Ljbffr MMS Holdings IncRemote jobSeniorRegulatory
$95k - $210.9k
Syneos Health/ inVentiv Health Commercial LLC is seeking a Sr. Principal Regulatory Medical Writer who will be responsible for developing regulatory documents for submissions worldwide, including Clinical Study Reports and Summaries of Efficacy and Safety. The ideal candidate...SeniorRegulatoryWorldwide$95k - $210.9k
...inVentiv Health Commercial LLC is seeking a Sr. Principal Regulatory Medical Writer in Arizona to develop regulatory documents, manage medical... ...ideal candidate will have extensive experience in preparing submissions for regulatory agencies globally and will be rewarded with...SeniorRegulatoryFlexible hours$95k - $210.9k
...Health/ inVentiv Health Commercial LLC is seeking a Sr. Principal Regulatory Medical Writer to join their team in California, Missouri. The candidate will develop regulatory documents for global submissions and manage medical writing projects, collaborating with cross-...SeniorRegulatory$95k - $210.9k
Syneos Health is seeking a Sr. Principal Regulatory Medical Writer with expertise in developing regulatory documents for global submission, particularly in oncology. Responsibilities include managing medical writing projects and participating in cross-functional meetings...SeniorRegulatoryFlexible hours$95k - $210.9k
...Health/ inVentiv Health Commercial LLC is looking for a Sr. Principal Regulatory Medical Writer with expertise in oncology. This role involves developing regulatory documents for global submission and managing medical writing projects. The candidate will work with cross...SeniorRegulatoryFlexible hours- Veristat seeks a Principal Medical Writer to independently plan and prepare regulatory documents and medical communications across product development stages... ...high‑quality documents for diverse regulatory submissions in a remote-friendly environment. #J-18808-Ljbffr...Remote workSeniorRegulatory
- 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... ...deliverables like clinical protocols, IND submissions, and more, adhering to regulatory standards. Applicants...Remote jobSeniorRegulatoryWork from home
- ...subsidiary of Eli Lilly and Company, is seeking a Senior Medical Writer to author and manage clinical regulatory documents across its development programs,... ...Biostatistics, Pharmacovigilance, and CMC teams to support submissions. #J-18808-Ljbffr Centessa Pharmaceuticals, a...SeniorRegulatory
- 6AM City, LLC is seeking an experienced Senior Medical Writer to join its team in Massachusetts. The role involves writing and editing clinical reports and documents required for regulatory submissions. Ideal candidates should have 10+ years of medical writing experience...SeniorRegulatory
- Syneos Health/ inVentiv Health Commercial LLC is seeking a Sr. Principal Medical Writer responsible for regulatory submission documents, specifically within the Oncology therapeutic area. You will lead medical writing projects, ensuring compliance with regulatory standards...SeniorRegulatory
$95k - $210.9k
Syneos Health/ inVentiv Health Commercial LLC is looking for a Senior Principal Medical Writer to oversee the development of clinical documents for regulatory submissions globally. This role requires at least 5 years of experience in medical writing within the biopharmaceutical...SeniorRegulatory- Prometrika, Llc in Cambridge, MA is seeking a Senior Medical Writer to create and edit clinical and scientific reports crucial for regulatory submissions. The ideal candidate will have at least 6 years in medical writing, including 4 years specifically in regulatory scenarios...SeniorRegulatory
- Itlearn360 is seeking a Senior Medical Writer in South San Francisco. This role involves overseeing high-quality documents for clinical trials and regulatory submissions. The ideal candidate should have 8-10 years of scientific writing experience, including expertise in...Remote jobSeniorRegulatoryHourly payTemporary work
- ...Health/ inVentiv Health Commercial LLC is looking for a Sr. Principal Medical Writer to develop high-quality clinical documents for global submissions. The role requires extensive knowledge of regulatory standards and substantial experience in the biopharmaceutical...SeniorRegulatoryFlexible hours
- ...inVentiv Health Commercial LLC is seeking a Sr. Principal Medical Writer to develop clinical documents for global submissions. Ideal candidates possess extensive medical writing experience and a strong knowledge of regulatory standards, particularly in oncology. This role...SeniorRegulatory
- Syneos Health/ inVentiv Health Commercial LLC seeks a Sr. Principal Medical Writer to lead the development of clinical documents for global regulatory submissions. The ideal candidate will possess strong medical writing experience, organizational skills, and the ability...SeniorRegulatoryFlexible hours
- Syneos Health, a leader in life sciences, is hiring a Sr. Principal Medical Writer for submissions to regulatory authorities. Responsibilities include developing clinical documents, providing strategic direction to teams, and mentoring junior staff. The ideal candidate...SeniorRegulatoryFlexible hours
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