Remote Oncology QC Medical Writer - Regulatory Docs
Sumitomo Pharma
- Remote job
Sumitomo Pharma America, Inc. is seeking a QC Medical Writer to perform QC audits of clinical regulatory documents and support the Medical Writing team. This role ensures QC findings are addressed and documents meet company standards. Primarily remote with periodic on-site meetings; travel domestically and internationally as needed. Requires minimum 3 years of QC experience in biotech/pharma, oncology experience preferred, and knowledge of GCP, FDA regulations, ICH guidelines, and AMA style #J-18808-Ljbffr Sumitomo Pharma
$100.9k - $126.1k
...addressing patient needs in oncology, urology, women's... ...Executive Director, Medical Writing Oncology and... ...for the position of QC Medical Writer. The QC Medical Writer... ...) review of clinical regulatory documents.... ...Requirements Primarily remote role with periodic on...Remote workRegulatoryWork experience placementWork at officeWorldwideFlexible hours- ...Senior Medical Writer/Principal Medical Writer The Senior Medical Writer... .../formatting, and performing QC review. Develops documents in... ..., Precision SOPs, applicable regulatory guidelines (ie, ICH, FDA, GCP... ...Advanced degree (MS/PhD) Oncology and/or rare disease experience...Remote workRegulatory
- ...professionals specializing in medical writing,... .... Synterex offers remote or on-site... ...The senior medical writer will partner cross... ...Operations, Biostatistics, Regulatory, and Program... ...quality control [QC], publishing) to ensure... ...a relevant field Oncology, Infectious...Remote workRegulatoryLocal area
- ...Medical Writer Celerion is committed to swift, exceptional clinical research... ...-time Medical Writer to work remotely. This position will analyze... ...safety text. Perform peer QC function of safety text prior... ...compliant with applicable regulatory standards (i.e. Good Clinical...Remote workRegulatoryFull time
$120k - $159k
...Company, is hiring Senior/Principal Medical Writers (USA) to support our growing company in producing regulatory documentation for the... ...time); may work either fully remotely or a hybrid schedule (in office... ...coordinating other writers and QC specialists assisting on documents...Remote workRegulatoryLive inWork at officeWork visa- ...Medical Writing Specialist For the past 25 years,... ...deep domain expertise in regulatory sciences, clinical research... ...experienced medical writers, as necessary.... ...deliverables. Coordinates QC reviews of documents and... ...Whilst ProPharma supports remote working, we also...Remote workRegulatoryContract workWork at office
- ...address significant unmet need in oncology and rare diseases. See Yourself at Telix The Medical Writer will contribute to the... ...preparing a variety of clinical and regulatory documents necessary for all... ...medicine. We have hybrid and remote employees located all around...Remote workRegulatory
$90k - $140k
...Senior Medical Writer Everest Clinical Research ("Everest") is a full... ...Canada on-site location, or remotely from a home-based office anywhere... ...documents supporting regulatory submissions for clinical trial... ...Follow up on the quality control (QC) findings until they are properly...Remote workRegulatoryContract workTemporary workWork from homeWorldwide- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy,... ...high-quality medical writing. This is a remote contractor role requiring strong writing...Remote jobRegulatoryFor contractors
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents with a focus on scientific accuracy and regulatory compliance. The role emphasizes high-quality medical writing, CSR authoring...Remote jobRegulatory
$70 - $80 per hour
...specializing in IT is looking for a Senior Medical Writer to manage the medical writing function.... ...drafting clinical study protocols, regulatory documents, and managing review timelines... .... This full-time position is primarily remote, with a competitive pay range of $70 -...Remote jobRegulatoryHourly payFull timeContract work- ...YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy... ...documentation quality initiatives within a remote contract setting. Strong written...Remote workRegulatoryContract workTemporary work
- YO AI Labs is seeking a Medical Writer Expert for a remote contract to develop, review, and evaluate clinical and regulatory documents with scientific precision and regulatory compliance... ...teams in a fast-paced environment. Oncology and haematology experience is preferred....Remote jobRegulatoryContract work
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy,... ...collaboration across cross-functional teams in a remote contractor capacity. #J-18808-Ljbffr YO...Remote jobRegulatoryFor contractors
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop and review regulatory documents with a focus on accuracy and compliance. The role involves interpreting protocols, ensuring ICH E3 alignment, and producing high-quality CSRs and related...Remote jobRegulatory
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. You will author and review CSRs...Remote jobRegulatory
- YO AI Labs is seeking an experienced Medical Writer Expert to develop, review, and evaluate clinical and regulatory documents remotely as a contractor. The role emphasizes scientific accuracy, regulatory compliance, and collaboration with cross-functional teams. You will...Remote jobRegulatoryFor contractors
- Veristat LLC is seeking a full-time Principal Medical Writer to independently plan and prepare regulatory documents and medical communications. This remote role involves supporting all phases of product development while collaborating with cross-functional teams. The ideal...Remote jobRegulatoryFull time
- ...pharmaceutical advertising agency, to find a Freelance Senior Medical Writer. This remote temporary role starts ASAP and goes until the end of year... ...promotional materials to ensure accuracy and regulatory compliance. Conduct detailed scientific fact-checking...Remote workRegulatoryTemporary workFreelanceImmediate start
$117k - $143k
...offering flexibility to work remotely and from our headquarters in Watertown... ...is seeking an experienced Medical Writer to lead and coordinate the scientific and clinical regulatory writing aspects of documents... ..., perform quality control (QC) review and substantive editing...Remote workRegulatoryFlexible hours- ...FSP has an exciting opportunity for a Medical Writer ! Key Accountabilities Author Clinical... ...finalize clinical documents for submission to regulatory authorities, including but not limited... ...Sciences or equivalent. #LI-KW1 #LI-REMOTE EEO Disclaimer Parexel is an equal...Remote workRegulatoryInterim roleFlexible hours
- ...Description THE POSITION: Medical Affairs is a key customer-... ...accuracy, editorial excellence, regulatory compliance, and data integrity... ...management. Partner with writers, MLR coordinators, and MLR reviewers... ..., proofreading, and final QC review, including source-to-...Remote workRegulatoryFull timeWork at officeLocal areaHome officeFlexible hoursShift work
- ...strategies for lab data collection and providing end-to-end analytical and logistical solutions. The Medical Writer is responsible for authoring clinical trial and regulatory documents, through independent assignment and oversight as well as engagement within a cross-...Remote workRegulatoryTemporary workLive outWork at officeFlexible hours
$85k - $98k
...Haymarket Media, Inc. is seeking a Medical Writer to join the PRI team. This... ...team flex day) and two days remote. Job Overview: The Medical... ...participate in client medical/legal/regulatory reviews as needed Maintain an... ...Google Suite such as Slides, Docs in addition to online medical...Remote workRegulatoryWork at officeLocal areaFlexible hours- A leading health research institute is seeking an experienced Source Writer with QA/QC/Regulatory expertise. You will ensure high standards of scientific excellence while contributing to transformative liver health initiatives. Responsibilities include generating source...Remote jobRegulatory
- Medical Writer II job at US Tech Solutions. Remote. Location: Remote. Duration: 12 months contract. Job Description Defines scope of quality control activities... ...processes. Maintain strong knowledge of clinical regulatory documents requiring quality control review and...Remote jobRegulatoryContract work
- ...Life Sciences with a focus in Hematology and/or Oncology research for a full-time, office-based Medical Writer position. The Medical Writer will lead development... ...and maintain high-quality, complex clinical and regulatory documents, including, but not limited to, clinical...RegulatoryFull timeWork at officeLocal areaFlexible hours
$150k - $211k
...approved medicines in oncology and other disease states... ...management, and global regulatory submissions of complex... ...various SMEs from MSAT, QA, QC, CMC, External... ..., US but will consider remote applicantsDomestic and... ...includes benefits such as medical, dental, vision, flexible...Remote workRegulatoryTemporary workWorldwideFlexible hours$175k - $205k
...Manager/Assoc Director, CMC Regulatory Affairs San Diego, CA,... ...San Francisco, CA or remote Erascais a clinical-stage precision oncology company focused on discovering... ...support through QC review of submission components... ..., and sick leave; medical, dental and vision plans...Remote workRegulatoryTemporary workCasual workLocal areaWorldwideFlexible hours- ...City headquarters, with some remote flexibility available. Duration... ...contract rates The Role The QC Lead performs rigorous quality... ...pharmacology submission documents and regulatory responses. Responsibilities... ...Direct experience in oncology drug development. Prior success...Remote workRegulatoryPermanent employmentFull timeContract workPart time
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