Senior Medical Writing Lead, Regulatory Submissions Remote
Travere Therapeutics
- Remote job
Travere Therapeutics in San Diego is looking for an Associate Director, Medical Writing to oversee regulatory submissions and manage related documentation. This role requires at least 6 years of experience in medical writing within the biopharmaceutical sector and a Master’s degree in a related field; a PhD or PharmD is preferred. The Associate Director will lead a team of medical writers, ensuring high-quality deliverables are completed on time. Strong writing and communication skills are critical, alongside knowledge of regulatory standards and project management abilities. Remote work is available, but face-to-face interactions in San Diego are essential. #J-18808-Ljbffr Travere Therapeutics
- ...seeking an Associate Director for Medical Writing to oversee regulatory submissions of critical documents related to life... ...to quality. This role will lead document development strategies and... ...junior writers. The position is mainly remote with a focus on collaboration...Remote workSeniorMedicalRegulatory
$150k - $195k
...Therapeutics is seeking an Associate Director, Medical Writing to oversee regulatory submissions and ensure compliance with medical writing standards. You will lead medical writing projects and... ...writing. This position is mainly remote but requires availability for virtual...Remote workSeniorMedicalRegulatory$150k - $195k
Travere Therapeutics is seeking an Associate Director, Medical Writing to oversee regulatory submissions. The candidate will manage medical writing projects,... ...skills are essential. This role allows for remote work but may require occasional travel. Competitive salary...Remote workSeniorMedicalRegulatory$150k - $195k
...Therapeutics is looking for an Associate Director, Medical Writing, responsible for leading regulatory submissions and ensuring high-quality documentation.... ...collaboration with cross-functional teams and entails remote work with some onsite presence in San Diego. #J-...Remote workSeniorMedicalRegulatory- ...Therapeutics is actively seeking a Senior Manager for Medical Writing. This role involves leading the creation and management of important regulatory documents while ensuring... ...writing and regulatory submissions. The position is partially remote and requires collaboration...Remote jobSeniorMedicalRegulatory
- Travere Therapeutics in San Diego is seeking an Associate Director of Medical Writing to oversee regulatory submissions and ensure compliance with writing standards. You will lead a team of writers and collaborate with cross-functional partners to deliver high-quality documents...SeniorMedicalRegulatory
- INC Research is seeking a Senior Medical Writer to support clinical study and regulatory project teams. This position is home... ...while managing complex medical writing tasks across various therapeutic... ...like clinical protocols, IND submissions, and more, adhering to regulatory...Remote jobSeniorMedicalRegulatoryWork from home
- Travere Therapeutics is seeking an Associate Director of Medical Writing to lead regulatory submission efforts, ensuring adherence to quality and strategic oversight. The role requires collaboration with cross-functional teams and involves authoring a range of regulatory...SeniorMedicalRegulatory
- Jobtailor in San Diego seeks a Senior Medical Writer with oncology focus to... ...and operational medical writing for complex clinical and regulatory documents. You will lead authoring and end-to-end development for health authority submissions. Requirements include a PhD preferred...SeniorMedicalRegulatory
- Itlearn360 is seeking a Senior Medical Writer in South San Francisco. This role involves overseeing... ...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
- Travere Therapeutics is seeking an Associate Director, Medical Writing to lead regulatory submissions, ensuring compliance and high-quality document delivery. In this role, you will provide strategic guidance, collaborate with cross-functional teams, and mentor junior...SeniorMedicalRegulatory
$150k - $195k
Travere Therapeutics is seeking an Associate Director, Medical Writing to lead the development and oversight of regulatory submissions. The ideal candidate will have at least 6 years of experience in medical writing within a biopharmaceutical environment. This position...SeniorMedicalRegulatory- Alnylam Pharmaceuticals is looking for a Senior Manager, Medical Writing to join our team in Cambridge, Massachusetts. This role involves... ...years of medical writing experience, familiarity with regulatory submissions, and excellent project management skills. A comprehensive...SeniorMedicalRegulatoryContract work
- Sobi in San Diego is seeking a Principal Medical Writer who will lead the authoring of clinical and regulatory documents. This role requires 8-10 years of experience, focusing on clarity and credibility in submissions to fulfill regulatory needs. The ideal candidate will...SeniorMedicalRegulatory
- A leading staffing firm is seeking a Medical Author to document clinical data and regulatory submissions to support drug development. This role requires expertise in analytical writing, project management, and collaboration with product teams to ensure high-quality deliverables...SeniorMedicalRegulatory
- A leading healthcare intelligence firm is seeking a Principal Medical Writer to lead the development of regulatory and clinical documents. The ideal candidate will... ...and significant medical writing experience, particularly in regulatory submissions. This role offers a...Remote jobMedicalRegulatoryFlexible hours
- GlaxoSmithKline is seeking a Principal Medical Writer for their Durham office. The ideal candidate will lead complex medical writing projects and collaborate with cross-functional teams on regulatory submissions. Key requirements include over 5 years in medical writing...Remote jobMedicalRegulatoryWork at office
$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- ...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 workSeniorMedicalRegulatoryFlexible hours
- ...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
- ...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 workSeniorMedicalRegulatoryFlexible hours
- 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. The role involves managing timelines and collaborating across functions to produce high-quality materials...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- 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...Remote jobSeniorMedicalRegulatory
- 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... ...complex research into regulatory documents and... ...experience in medical writing and a strong background... ...with the potential for remote work. #J-18808-Ljbffr...Remote workSeniorMedicalRegulatory$137.2k - $205.8k
...Pharmaceuticals in Boston is looking for a Medical Writing Science Senior Manager to independently author... ...documents. This hybrid role allows for remote work two days a week, ensuring flexibility while leading critical regulatory writing activities. The ideal candidate...Remote workSeniorMedicalRegulatory2 days per week$121k - $185k
...compliance story. As our Senior GRC Security Lead, you will be the... ...aligned with evolving regulatory requirements, industry... ...policy and standards writing ability — capable of... ...Gongsters a variety of medical, dental, and vision... ...help you succeed in a remote environment. The...Remote workSeniorMedicalRegulatoryWork from homeFlexible hours$132k - $172k
Travere Therapeutics in San Diego is seeking a Senior Manager, Medical Writing to oversee the authoring and management of regulatory, clinical, and safety documents. This role requires leadership in document strategy and adherence to compliance while working closely with...SeniorMedicalRegulatory
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