Veeda Clinical Research (Veeda CR), a leading Contract Research Organization (CRO), is inviting applications for the role of Report Writer in its Biopharmaceutics & Project Management Department. This full-time opportunity is perfect for pharma professionals with experience in medical writing, regulatory submissions, and clinical study reporting.
Advertisement
If you’re looking to advance your career in clinical research with a reputed CRO, this opening offers the right platform.
Key Responsibilities
As a Report Writer at Veeda CR, you will:
- Prepare clinical study reports of BABE and patient-based clinical trials (PK/PD/clinical endpoint studies).
- Finalize project reports with appendices as per eCTD guidelines (Modules 2 & 5).
- Submit final compilations with eCTD compliance to clients.
- Collaborate with Project Managers, Bioanalytical teams, and Statisticians to compile complete reports.
- Draft final reports, address sponsor comments, and ensure timely submission.
Qualifications & Requirements
- Education:
- UG: B.Pharm (Any Specialization)
- PG: M.Pharm (Any Specialization)
- Experience: 1–3 years in medical writing, clinical research, or regulatory submissions.
- Skills:
- Knowledge of eCTD submission process
- Understanding of regulatory standards, SOPs, and client reporting templates
- Strong coordination and documentation abilities
Benefits of Working with Veeda CR
- Competitive salary: ₹3–5 LPA
- Opportunity to work on global clinical research projects
- Exposure to regulatory submissions and eCTD
- Collaborative work culture in a reputed CRO
How to Apply
Advertisement
