Senior Medical Writing Lead - Regulatory & Clinical (Remote)
Travere Therapeutics
Detroit, MI
- Remote job
Travere Therapeutics is looking for a Senior Manager, Medical Writing to lead the creation and management of regulatory documents. This role involves ensuring scientific accuracy, compliance, and timely delivery of documents across clinical development phases. The ideal candidate will have at least 7 years of experience in medical writing, excellent writing and communication skills, and a deep understanding of drug development processes. A bachelor's degree in Life Sciences is required, with advanced degrees preferred. Benefits include comprehensive health plans, retirement options, and competitive pay. #J-18808-Ljbffr Travere Therapeutics
Vacancy posted 3 days ago
Similar jobs that could be interesting for youBased on the Senior Medical Writing Lead - Regulatory & Clinical (Remote) in Detroit, MI vacancy
$132k - $172k
Travere Therapeutics is seeking a Senior Manager, Medical Writing to lead the creation of regulatory, clinical, and safety documents. This role provides strategic guidance and ensures compliance, with responsibilities spanning all phases of clinical development. The ideal...Remote jobSeniorMedicalRegulatory- Travere Therapeutics is seeking a Senior Manager, Medical Writing to lead the creation and management of regulatory, clinical, and safety documents. This role ensures scientific accuracy, regulatory compliance, and timely delivery of all materials. The ideal candidate will...Remote jobSeniorMedicalRegulatory
$132k - $172k
Travere Therapeutics is seeking a Senior Manager in Medical Writing to lead the development of critical regulatory documents, ensuring scientific accuracy and compliance.... ...functions to produce high-quality materials for clinical programs. With a requirement of at least 7...Remote jobSeniorMedicalRegulatory- Travere Therapeutics is actively seeking a Senior Manager for Medical Writing. This role involves leading the creation and management of important regulatory documents while ensuring scientific... .... The position is partially remote and requires collaboration with cross...Remote jobSeniorMedicalRegulatory
$132k - $172k
Travere Therapeutics is seeking a Senior Manager, Medical Writing, to lead the creation and management of regulatory documents. Responsibilities include ensuring scientific... ...comprehensive benefits. This position is primarily remote, but some on-site presence in San Diego is...Remote jobSeniorMedicalRegulatory- ...Veristat, a leading clinical research organization in the United States, seeks a Senior Medical Writer – Clinical Focus to lead document authorship across service lines... ...as part of a delivery team. You will guide regulatory documentation, ensure adherence to guidelines...Remote workSeniorMedicalRegulatory
Veristat
Oklahoma City, OK3 days ago - A leading global clinical research organization is seeking a Senior Medical Writer I for a 12-month FTC, fully remote. In this role, you will spearhead the development... ...execution of medical writing initiatives supporting... ...communication and regulatory knowledge. Competitive...Remote jobSeniorMedicalRegulatoryFixed term contract
$89k - $148k
A leading healthcare company is seeking an experienced medical writer to lead projects for Clinical Research Scientists and other stakeholders... ...research into regulatory documents and... ...experience in medical writing and a strong... ...the potential for remote work. #J-18808-Ljbffr...Remote workSeniorMedicalRegulatory- 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... ...mentor junior writers while managing complex medical writing tasks across various therapeutic areas. The role...Remote jobSeniorMedicalRegulatoryWork from home
$106k - $149k
...Lifesciences Belgium is seeking a Sr. Specialist in Clinical Science/Medical Writing. This role focuses on supporting regulatory and clinical document development for the... ...affairs are required. This position is US Remote based and offers competitive pay ranging from...Remote workSeniorMedicalRegulatoryEdwards Lifesciences
Phoenix, AZ3 days ago$106k - $149k
...Edwards Lifesciences Belgium is seeking a Sr. Specialist in Clinical Science/Medical Writing to support regulatory and clinical documentation for TMTT products. This US remote position involves literature searches, data extraction, and document development to optimize...Remote workSeniorMedicalRegulatoryEdwards Lifesciences Belgium
Seattle, WA3 days ago$137.2k - $205.8k
...Pharmaceuticals in Boston is looking for a Medical Writing Science Senior Manager to independently author complex clinical study documents. This hybrid role allows for remote work two days a week, ensuring flexibility while leading critical regulatory writing activities. The ideal...Remote workSeniorMedicalRegulatory2 days per week- Itlearn360 is seeking a Senior Medical Writer in South San Francisco. This role involves... ...high-quality documents for clinical trials and regulatory submissions. The ideal candidate should have 8-10 years of scientific writing experience, including expertise in neuromuscular...Remote jobSeniorMedicalRegulatoryHourly payTemporary work
$116k - $128k
...Strategies, LLC is looking for a Senior Medical Writer specializing in clinical documentation. This role involves leading document authorship,... ...and over 3 years of regulatory writing experience. A strong proficiency... ...benefits including remote work options and medical...Remote workSeniorMedicalRegulatorySynchrogenix Information Strategies
Oklahoma City, OK4 days ago- Precision Medicine Group seeks a Senior Medical Writer to lead development of high-quality clinical study documents, ensuring on-time delivery and regulatory compliance across ICH, FDA, GCP and... ...Responsibilities include planning, writing, editing, formatting, and QC of...SeniorMedicalRegulatory
- A biotech research company in South San Francisco seeks an Associate Director of Medical Writing to lead the development of high-quality clinical and regulatory documents. The ideal candidate must possess a Master's degree and over 8 years of experience in scientific writing...SeniorMedicalRegulatory
- MMS Holdings Inc is seeking an experienced Medical Writer located in Bridgeport, Connecticut, to... ...pharmaceutical and biotech industries. The role involves writing clinical development documents and requires a strong background in regulatory writing alongside exceptional writing and...Remote jobSeniorMedicalRegulatory
- 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 jobSeniorMedicalRegulatory
- RegDev, Inc. is seeking an experienced Medical Writer Consultant to assist in authoring clinical protocols and regulatory filings. This position demands expertise in translating... .... The role offers flexibility, with the potential for remote work. #J-18808-Ljbffr RegDev, Inc.Remote workSeniorMedicalRegulatory
- Edwards Lifesciences is seeking a Sr. Specialist in Clinical Science/Medical Writing to support regulatory and clinical documents for their Transcatheter Mitral... ...of experience in medical or clinical affairs. This remote position offers competitive salaries and a wide range...Remote workSeniorMedicalRegulatory
- ...Holdings Inc is looking for a skilled Medical Writer to join their team in Atlanta, Georgia... ...minimum of 3-5 years of experience in regulatory writing within the pharmaceutical industry and... ...medical literature, writing various clinical documents, and mentoring junior writers...Remote jobSeniorMedicalRegulatory
- 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 jobSeniorMedicalRegulatory
- 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 jobSeniorMedicalRegulatory
- Precision Medicine Group seeks a Senior Medical Writer/Principal Medical Writer to lead development of clinical study documents with high quality and on-time delivery. The role emphasizes planning, writing, editing, formatting, and QC across protocols, IBs, ICFs, DSURs...Remote jobSeniorMedical
$116k - $128k
Veristat, LLC. is looking for a Senior Medical Writer with a clinical focus, responsible for leading document authorship across... ...demands a strong background in regulatory writing and clinical documentation,... ...to $128K and provides a fully remote working option. Benefits...Remote jobSeniorMedicalRegulatoryFlexible hours- ...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... ...scientific field and experience in leading teams. This role is vital in...Remote jobSeniorMedicalRegulatory
- ...Durham, North Carolina is seeking a Principal Medical Writer to lead regulatory document preparation for complex clinical projects. This role demands excellent communication... ...skills and a strong background in medical writing, with a focus on HIV-related treatments. You...Remote jobMedicalRegulatory
$270k - $360k
...Medical Director/Senior Medical Director, Clinical Development TenvieTherapeutics is developing... ...Director to lead early‑ and mid‑... ...This role can be remote, hybrid, or on‑site... ...quality clinical and regulatory documentation Lead... ...and medical writing skills; able to produce...Remote workSeniorMedicalRegulatoryLocal areaTenvie Therapeutics
South San Francisco, CA2 days ago- ...Reports to: Clinical Affairs Manager Workplace... ...Us At Capstan Medical, we are driven by... ...We are seeking a Senior Clinical Research... ...sites, engineering, regulatory teams, biostatisticians... ...on-site and remote site qualification... ...ICF development, writing clinical sections...Remote workSeniorMedicalRegulatoryInterim roleWork at officeFlexible hours
Capstan Medical, Inc.
Santa Cruz, CA23 hours ago - ...Health/ inVentiv Health Commercial LLC is seeking a Sr Medical Writer for remote-based work. The role involves leading the medical writing efforts for scientific documents and ensuring compliance with regulatory standards. The ideal candidate will possess strong medical...Remote workSeniorMedicalRegulatoryFlexible hours
Syneos Health/ inVentiv Health Commercial LLC
Virginia, MN4 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Medical Writing Lead - Regulatory & Clinical (Remote). Be the first to apply!
Related searches
- senior app developer Detroit, MI
- senior international account manager Detroit, MI
- senior magento developer Detroit, MI
- senior quantitative risk analyst Detroit, MI
- senior business development director Detroit, MI
- sr marketing manager Detroit, MI
- sr technical product manager Detroit, MI
- senior information technology consultant Detroit, MI
- senior manager pmo Detroit, MI
- senior accountant part time Detroit, MI