Bachwell Pharma is hiring a Research Scientist – Clinical R&D (Clinical Data Management) for its Pharma Formulation R&D division supporting global regulatory markets. This is an excellent opportunity for M.Pharm (Clinical) professionals with 2–5 years of experience who want to work at the intersection of clinical trials, formulation development, and global regulatory submissions.
Based at ALEAP, Hyderabad, this role plays a critical part in ensuring high-quality, compliant, and submission-ready clinical data for new drug products including tablets, injectables, and topical formulations.
📌 Job Overview
- Position: Research Scientist – Clinical R&D
- Department: Clinical Data Management (Pharma Formulation R&D)
- No. of Vacancies: 01
- Experience: 2–5 Years
- Qualification: M.Pharm (Clinical)
- Location: ALEAP, Hyderabad, India
- Industry: Pharmaceutical Research & Development
- Market Exposure: Global (FDA, EMA, PMDA)
🔬 Key Responsibilities – Clinical Data Management (CDM)
Research Scientist (Clinical R&D – CDM)
As a Research Scientist, you will act as the data architect for clinical studies supporting formulation R&D:
- Design and configure clinical databases using EDC systems such as Oracle Clinical or Medidata Rave
- Develop Case Report Forms (CRFs) aligned with formulation-specific endpoints (adherence, excipient safety, application site data)
- Perform data cleaning and query management, resolving discrepancies with clinical sites
- Conduct User Acceptance Testing (UAT) to validate edit checks and database logic
- Ensure data accuracy, consistency, and traceability throughout the study lifecycle
- Support database lock and clinical data handover to biostatistics teams
This Clinical Data Management job in Pharma R&D directly supports global regulatory filings and formulation performance evaluation.
🎓 Qualifications & Skills Required
- M.Pharm (Clinical) – Mandatory
- 2–5 years of experience in Clinical Data Management or Clinical R&D
- Hands-on experience with EDC systems (Oracle Clinical, Medidata Rave, or equivalent)
- Strong understanding of GCP guidelines and clinical trial workflows
- Working knowledge of CDISC standards (SDTM/ADaM) preferred
- Excellent communication skills for cross-functional coordination
🌍 Why Join Bachwell Pharma?
- Opportunity to work on global formulation R&D projects
- Direct exposure to FDA, EMA, and PMDA-aligned clinical studies
- Career growth in Clinical Data Management for global markets
- Scientifically driven environment with a focus on innovation and compliance
- Work location in Hyderabad’s ALEAP pharma R&D ecosystem
💰 Salary & Benefits
- Estimated Salary Range: ₹6,00,000 – ₹10,00,000 per annum (CTC)
- Performance-linked growth opportunities
- Exposure to global regulatory submissions
- Professional development in clinical and regulatory domains
(Salary may vary based on experience and technical expertise.)
📧 How to Apply
Interested and eligible candidates can apply by sending their updated CV to:
📱 WhatsApp Contact: +91 9014502249
⚠️ Only shortlisted candidates will be contacted. Bachwell Pharma prioritizes profiles already available in its internal database when relevant opportunities arise.
