Sr Medical Writer, Redaction (Clinical Trial Transparency)
$80.6k - $145kSyneos Health Inc
Sr Medical Writer, Redaction (Clinical Trial Transparency) Updated: April 29, 2026 Location: Morrisville, NC, United States Job ID: 25105719-OTHLOC-1500-2DMD-2DR The Sr Medical Writer will focus on the redaction and quality assurance of clinical trial transparency documents, ensuring compliance with regulatory submission standards and company processes. The role requires meticulous attention to detail, strong written communication skills, and the ability to work collaboratively with multidisciplinary teams. Job Responsibilities Executes project specific activities with high quality and in defined timelines according to standard processes and operating procedures. Marks, quality assures, reviews and edits pertinent documents such as clinical study reports, patient narratives, clinical summaries, and other regulatory submissions for regulations including EMA policy 0070, Health Canada PRCI, EUCTR, and NIH final rule. Prepares protocol and results summaries to support clinical trial disclosure commitments. Systematically performs quality control checks of documents prepared by colleagues against pre‑specified checklists generated in the project or SOP. Performs detailed analyses on a planned and ad hoc basis, relating to processes and their outputs. Ensures adherence to client processes and requirements. Completes internal and client‑specific training as required. Assists in mentoring and training of team members depending upon project requirements. Benefits Benefits may include a company car or car allowance, medical, dental, and vision coverage, 401(k) matching, employee stock purchase plan eligibility, commission/bonus opportunities, and flexible paid time off and sick time per state regulations. Salary Range $80,600.00 - $145,000.00 Additional Information Tasks, duties, and responsibilities listed are not exhaustive. The Company may assign additional duties at its discretion. Equivalent experience, skills, or education may also be considered. The Company is committed to compliance with the Americans with Disabilities Act and provides reasonable accommodations when appropriate. #J-18808-Ljbffr Syneos Health Inc
$80.6k - $145k
Sr Medical Writer, Redaction (Clinical Trial Transparency) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization...SeniorContract workFlexible hours$80.6k - $145k
Syneos Health, Inc. is looking for a Sr Medical Writer specializing in redaction for clinical trial transparency. Located in Morrisville, NC, the role involves ensuring compliance with regulatory standards and providing quality assurance on various clinical documents. Ideal...SeniorFlexible hours$95k - $210.9k
Sr. Principal Regulatory Medical Writer - Oncology Preferred Updated: Yesterday Location: Morrisville, NC, United States Job ID: 25108891-OTHLOC-1500-... ...complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug‑development...SeniorContract workFlexible hours$80.6k - $145k
...Leads the clear and accurate completion of medical writing deliverables, ensuring... ...a variety of documents that may include clinical study protocols and protocol amendments;... ...Mentors and leads less experienced medical writers on complex projects. Develops deep expertise...SeniorContract workFlexible hours- Principal Medical Writer - Publications As a Principal Medical Writer at Syneos Health, you will lead the development, review, and finalization of a broad range of medical documents for clinical studies and regulatory submissions. You will collaborate closely with clinical...SuggestedContract work
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- Syneos Health, Inc. is seeking a Sr. Principal Regulatory Medical Writer located in Morrisville, NC. You will develop regulatory submissions, manage writing projects, and collaborate with cross-functional teams to ensure high-quality deliverables. The ideal candidate will...Senior
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