Veeda Clinical Research (Veeda CR), a leading clinical research organization in India, is hiring for two key positions in the Biopharmaceutics Department at its Ahmedabad facility. These roles are ideal for B.Pharm / M.Pharm graduates with experience or strong exposure to clinical research, ICH-GCP guidelines, QC documentation, and clinical study report writing.
This is an excellent opportunity for early-career professionals seeking long-term growth in clinical research, regulatory documentation, and biopharmaceutics quality operations.
🧪 Open Positions at Veeda CR
1️⃣ Quality Control – Biopharmaceutics Department
Experience: 0–2 Years
CTC: ₹3 – 4 LPA
Openings: 1
Location: Ahmedabad
🔹 Key Responsibilities
- Review and comment on clinical trial protocols, Informed Consent Documents (ICDs), CRFs, and related documents as per SOPs and ICH-GCP guidelines
- QC review of clinical study reports, appendices, and final e-CTD submissions
- Ensure documents are reviewed within defined timelines and priorities
- Review sponsor comments and regulatory observations; ensure timely responses
- Review and implement departmental SOPs and process updates
- Ensure corrective and preventive actions (CAPA) for QC findings
- Coordinate with cross-functional teams and reporting managers
2️⃣ Report Writer – Biopharmaceutics Department
Experience: 1–3 Years
CTC: ₹3.5 – 5.5 LPA
Openings: 2
Location: Ahmedabad
🔹 Key Responsibilities
- Prepare Clinical Study Reports (CSR) for BA/BE studies and patient-based clinical trials (PK, PD, clinical endpoint studies)
- Compile e-CTD submissions, including:
- Module 2 – Summary Reports
- Module 5 – Clinical Study Reports, appendices, literature, BR reports
- Coordinate with Project Managers, Sponsors, Bioanalytical, and Statistics teams
- Address sponsor comments and submit finalized reports as per SOPs and regulatory standards
- Ensure compliance with ICH-GCP, regulatory guidelines, and client templates
🎓 Eligibility & Qualifications
- UG: B.Pharm (Any Specialization)
- PG: M.Pharm / MS / M.Sc (Science)
- Knowledge of ICH-GCP, clinical research processes, and regulatory documentation
- Strong attention to detail, compliance mindset, and documentation skills
💼 Why Join Veeda CR?
- Work with a reputed global clinical research organization
- Exposure to regulatory-compliant clinical documentation and e-CTD submissions
- Structured SOP-driven environment enhancing regulatory expertise
- Competitive salary aligned with industry standards
- Long-term career growth in clinical research & biopharmaceutics
📨 How to Apply
Application Link For Quality Control – Biopharmaceutics Department
Application Link For Report Writer – Biopharmaceutics Department