Senior Medical Writer - Regulatory & Clinical Documentation
Syneos Health, Inc.
Syneos Health, Inc. is looking for a Senior Medical Writer based in Morrisville, NC. This role involves writing, editing, and coordinating clinical and regulatory documents while serving as a technical contact. Candidates should possess strong medical writing skills with 3–5 years of experience in the biopharmaceutical or CRO industry. In this full-time position, you will lead writing deliverables, coordinate activities across departments, and mentor junior writers. Benefits include medical coverage, 401(k) matching, flexible PTO, and various other perks. #J-18808-Ljbffr Syneos Health, Inc.
$80.6k - $145k
...Senior Medical Writer - Regulatory Documents - CSR /Protocol - Late Phase Syneos Health is a leading fully-integrated life sciences services organization... ...complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development...SeniorRegulatoryContract workFlexible hours- ...Syneos Health, Inc. is seeking a Senior Medical Writer in Morrisville, NC, to lead and execute... ...across departments to meet regulatory standards. The ideal candidate will... ...capability to produce critical documentation, including clinical study protocols and regulatory submissions...SeniorRegulatory
$80.6k - $145k
...Health, Inc. is looking for a Sr Medical Writer specializing in redaction for clinical trial transparency. Located in Morrisville... ...ensuring compliance with regulatory standards and providing quality assurance on various clinical documents. Ideal candidates are detail-...SeniorRegulatoryFlexible hours- ...TG Therapeutics, Inc. in Morrisville, North Carolina is seeking an experienced Medical Writer to develop and manage high-quality clinical, regulatory, and scientific documents. This role involves close collaboration with cross-functional teams in a biotechnology environment...SeniorRegulatoryFull timeContract work
$95k - $210.9k
Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred Syneos Health® is a leading fully-integrated... ...I is responsible for the development of clinical documents for submissions to regulatory authorities...SeniorRegulatoryContract workFlexible hours$80.6k - $145k
Sr Medical Writer, Redaction (Clinical Trial Transparency) Syneos Health® is a leading fully-integrated life... ...QC/Review and/or editing of pertinent documents such as: Clinical study documents or any other documents for regulatory submission i.e., clinical study...SeniorRegulatoryContract workFlexible hours- ...Syneos Health, Inc. is seeking a Sr. Principal Regulatory Medical Writer located in Morrisville, NC. You will develop regulatory submissions... ...candidate will have substantial experience in regulatory documentation and strong project management skills, with eCTD submission...SeniorRegulatory
$70.1k - $145k
...Syneos Health, Inc. is looking for a Medical Writer II to lead the creation and management of critical medical documents. This role requires 3-5 years of relevant experience... ...writing and a strong understanding of FDA regulatory standards. Responsibilities include...SeniorRegulatoryFlexible hours$80.6k - $145k
...Syneos Health/ inVentiv Health Commercial LLC is seeking a Senior Medical Writer specializing in regulatory documents, responsible for leading the medical writing process for clinical studies and ensuring document accuracy against regulatory standards. The ideal candidate...SeniorRegulatoryFlexible hours- ...expertise that empowers biotech, medical device, and pharmaceutical... ...deep domain expertise in regulatory sciences, clinical research solutions,... ...diagnostics, or disclosures documents) across all phases of... ...less experienced medical writers, as necessary. Adhere to established...SeniorRegulatoryContract work
- ProPharma in Raleigh, North Carolina, seeks a skilled medical writer with at least 5 years of experience. The role involves authoring a variety of clinical and regulatory documents while ensuring adherence to regulatory standards. The ideal candidate will demonstrate strong...SeniorRegulatory
$95k - $210.9k
Sr. Principal Regulatory Medical Writer - Oncology Preferred Updated: Yesterday Location: Morrisville, NC, United... ...Job Responsibilities Develop regulatory documents for submission to regulatory agencies globally—including Clinical Study Reports, Clinical Summaries of...SeniorRegulatoryContract workFlexible hours$84.4k - $211.1k
...Senior Medical Writer page is loaded## Senior Medical Writerlocations: Durham, North... ...writing projects. Prepares assigned documents in accordance with IQVIA... ...medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments...SeniorRegulatoryFull timePart timeLocal areaImmediate startWorldwide- GlaxoSmithKline in 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...RegulatoryRemote job
$62k - $108.6k
Sr. Medical Editor (Regulatory Documents + QC) - US Home based Syneos Health® is a leading fully-integrated... ...and accelerate progress. Our Clinical Solutions team members act with a drug... ...projects and updates the lead medical writer, project manager, and/or direct...SeniorRegulatoryContract workWork from homeFlexible hours- ...Syneos Health, Inc. is seeking a Principal Medical Writer to lead the development and finalization of medical documents for clinical studies and regulatory submissions. The role involves collaborating with clinical and medical teams to ensure clarity and compliance. Key...Regulatory
- ...ProPharma seeks an experienced Medical Writer in Raleigh, NC, to author and manage medical writing deliverables across clinical research phases. The ideal candidate will have at... ...least 5 years of experience in clinical or regulatory writing and a Bachelor's degree in a...SeniorRegulatoryRemote work
- 1001 Syneos Health, LLC is seeking a Clinical Research Associate II to manage site activities, ensuring compliance with regulatory requirements and ICH/GCP guidelines. The role... ...site qualification, monitoring, and documentation activities. Ideal candidates hold a Bachelor...SeniorRegulatoryRemote work
- ...Senior Manager, Clinical Data Management Department: Clinical Employment Type... ...data quality, integrity, and regulatory compliance throughout the... ..., biostatistics, medical monitoring, regulatory affairs... ...management, including TMF documentation. Identify process improvement...SeniorRegulatoryFull timeTemporary workWork at officeHome officeFlexible hours
$80.6k - $145k
...organization located in Morrisville, NC is seeking an experienced Medical Writer to ensure the accurate completion of medical writing... ...role involves managing complex writing projects, adhering to regulatory standards, and mentoring junior writers. The successful candidate...SeniorRegulatory- .../inVentiv Health Commercial LLC is looking for a Medical Writer in North Carolina. This role involves leading medical... ...writing deliverables, managing activities for clinical studies, and ensuring compliance with regulatory standards. The ideal candidate should have 3-5...SeniorRegulatory
- ...Aerogen is looking for a Clinical Trial Manager (CTM) in Morrisville, NC to manage multiple aspects of clinical trials, including study... ..., and vendor oversight. The CTM will ensure compliance with regulatory standards, handle subject safety, and facilitate successful trial...SeniorRegulatory
- Providence Health and Services is seeking a Clinical Documentation Specialist, Registered Nurse (RN) in a remote position. This role involves... ...quality reviews for OASIS admission documents and ensuring regulatory compliance. Ideal candidates must hold an Oregon RN License...RegulatoryRemote job
- ...Syneos Health, Inc. is seeking an Experienced Clinical Research Associate based in Morrisville, NC. The role involves overseeing the... ...qualification and monitoring activities to ensure compliance with regulatory standards. The ideal candidate will hold a Bachelor’s degree...SeniorRegulatoryFlexible hours
- Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator... ...adherence to protocols and regulatory guidelines. Responsibilities... ...and submitting regulatory documents, managing subject recruitment... ...skills. We provide medical benefits, paid time off, and...SeniorRegulatory
- ...A leading biopharmaceutical solutions organization is seeking an Experienced Clinical Research Associate to oversee site monitoring, ensuring compliance with regulatory requirements and clinical protocols. Responsibilities include conducting site visits, managing site...SeniorRegulatoryRemote workWorldwide
- ...Clinical QA Systems and Documentation Specialist Location: NC-RTP, US Contract Type: Regular Full-Time Area... ...documentation to meet company and regulatory requirements. Process change... ...pregnancy, childbirth, or related medical conditions; status as a protected veteran...RegulatoryFull timeContract workWork at office
- ...Clinical Documentation Principal Trainer Clinical Documentation Principal Trainer responsible for developing and delivering EHR training,... ...simulations Ensure training content aligns with system updates, regulatory requirements, and organizational standards EHR &...Regulatory
$49.34 - $76.59 per hour
Position Clinical Documentation Specialist, Registered Nurse (RN) - Providence Home Services Oregon... ...and Home Health leadership to promote regulatory compliance, patient outcomes, and reimbursement... ...Care. Experience with an Electronic Medical Record (EMR) system. Preferred...RegulatoryHourly payFull timeRemote workShift workDay shiftWeekday work- A leading clinical development firm in Raleigh, North Carolina is seeking a professional to provide... ...understanding of clinical trials and regulatory submissions. This role involves coordinating data, writing clinical documents, and ensuring effective communication across...SeniorRegulatory
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