Syneos Health require Medical Writer

Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers achieve their objectives.

Post : Medical Writer II (MLR Reviewer)

Job Description
• Mentors less experienced medical writers on projects, as necessary.
• Performs E2E process related scientific writing that includes but not limited to manage workflow in PubConnect, create publication plan, author approvals, pre-submission queries, submission activities etc.
• Veeva Vault document management - Creates placeholders, upload versions, reference linking, anchoring and linking, monitors the workflows/task completion.
• Reviews documents intended for Veeva submission and ensures they are fully MLR ready by proactively identifying and highlighting content changes needed per standards and guidelines, verifying claims against referenced sources, and streamlining the MLR review process to support first round approval.
• Compiles, writes, and edits medical writing deliverables, and serves as a medical writer within and across departments with minimal supervision.
• Develops or supports a variety of documents that include but not limited to:
• Clinical journal manuscripts, clinical journal abstracts, posters, and oral presentations.
• Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency.
• Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.
• Serves as peer reviewer on internal review team. Addresses team comments accurately to ensure document scientific content, clarity, overall consistency, and proper format.
• Adheres to established regulatory standards, including but not limited to congress/journal guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.

Performs on-line clinical literature searches, as applicable
• Familiarity with publication planning software e.g. Datavision and PubConnect (VeevaVault PromoMats or Medcomms).
• Continues professional development to keep pace with regulatory guidance and client expectations in medical writing that affect medical writing.
• Stays aware of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.
• Completes required administrated tasks within the specified timeframes.
• Performs other work-related duties as assigned.
• Minimal travel may be required (less than 25%).

Additional Information
Location : IND-Remote
IND-Gurugram-Hybrid
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : MLR Reviewer
End Date : 10th October 2026