Job Title: Medical Editor II – Clinical Pharmacology (CSR, IB, Protocol)
Location: Remote, India
Job ID: 25104357
Category: Medical Writing / Clinical Research
Company Overview:
Syneos Health® is a leading global biopharmaceutical solutions organization committed to accelerating clinical development and improving patient outcomes. Operating across 110 countries with 29,000 employees, we combine clinical, medical affairs, and commercial expertise to deliver high-quality, compliant solutions for clinical trials and regulatory submissions.
Role Overview:
We are seeking a Medical Editor II with experience in clinical pharmacology to ensure the accuracy, clarity, and regulatory compliance of critical study documents, including Clinical Study Reports (CSRs), Investigator Brochures (IBs), and protocols. This role focuses on copyediting, quality review, and document management with minimal supervision, ensuring deliverables meet client, regulatory, and industry standards.
Key Responsibilities:
Maintain familiarity with FDA, EMA, and other regulatory guidelines to ensure all documents comply with sponsor and regulatory expectations.
Represent the editorial team in medical writing and cross-departmental project teams as needed.
Monitor project timelines and budgets, providing updates to lead medical writers, project managers, or supervisors when deliverables are at risk.
Copyedit documents for grammar, punctuation, spelling, style (following AMA Manual of Style or custom guidelines), and internal quality standards.
Perform quality reviews of documents to ensure scientific accuracy, consistency, and clarity.
Manage assigned projects according to medical writing SOPs, client standards, and budget requirements with minimal supervision.
Compile medical writing deliverables when required, ensuring content integrity and adherence to submission standards.
Collaborate with medical writing leadership and project teams to resolve content or process issues efficiently.
Qualifications:
Bachelor’s or advanced degree in Life Sciences, Pharmacy, or a related scientific discipline.
3–5 years of experience in medical editing or scientific writing, preferably in clinical pharmacology or clinical research.
Strong knowledge of clinical trial documents (CSR, IB, protocols) and regulatory requirements.
Familiarity with medical writing SOPs, submission standards, and journal/conference guidelines.
Excellent written and verbal communication skills with attention to detail.
Ability to manage multiple assignments independently while adhering to timelines.
Strong organizational and interpersonal skills to work effectively with cross-functional teams.
Why Join Syneos Health:
Work on high-impact clinical trials with global reach.
Access career development, technical training, and recognition programs.
Thrive in an inclusive culture that values diversity, collaboration, and authenticity.
Contribute to the quality and compliance of regulatory and scientific documents across therapeutic areas.
How to Apply:
Apply now to join Syneos Health as a Medical Editor II and play a key role in delivering high-quality clinical pharmacology documents for global clinical development.
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