Looking to start your career in clinical data management jobs in India? Here’s an excellent opportunity for freshers and early-career professionals. Ascentrik Research Services is hiring a Clinical Data Associate in Pune (Wakad) for candidates with a strong background in clinical research, clinical trials, and data analysis.
This role is ideal for candidates aiming to build expertise in clinical trial data management, drug development processes, and secondary research within the pharmaceutical and life sciences industry.
Advertisement
📌 Job Overview
- Role: Clinical Data Associate
- Company: Ascentrik Research Services
- Location: Pune (Wakad)
- Experience: 0–1 Years
- Salary: ₹1.5–2 LPA
- Openings: 5
🔬 Key Responsibilities
- Organize and monitor clinical trial phases across multiple drug studies
- Track updates from clinical trial registries (ClinicalTrials.gov, PubMed, etc.)
- Perform clinical data collection, validation, and quality checks (100%)
- Analyze data related to efficacy, safety, biomarkers, and bioavailability
- Extract insights from scientific publications, conferences, and reports
- Maintain accurate documentation for clinical data management workflows
- Coordinate changes and updates in ongoing clinical research projects
- Work in a deadline-driven environment handling multiple assignments
🎓 Qualifications & Eligibility
Required:
- M.Pharm (Pharmaceutics, Pharmacology) OR
- M.Sc (Biotech, Microbiology, Biochemistry, Molecular Biology, Clinical Research, Genetics, Immunology, Drug Development)
Preferred:
- Candidates with published research papers
- Knowledge of drug development and clinical trials
- Familiarity with pre-clinical and clinical studies
- Strong Excel and analytical skills
- Experience in secondary research
Also Eligible:
- B.Pharm + 1 year experience in clinical research/clinical data management
Not Eligible:
- Pharmacognosy (M.Pharm)
- Botany, Zoology, Environmental Science, Ecology (M.Sc)
🧠 Required Skills
- Clinical Data Management
- Clinical Research & Clinical Trials
- eTMF (Electronic Trial Master File)
- Scientific literature review
- Data validation and quality assurance
- Strong communication skills
💼 Why This Role is Valuable
- Entry into high-demand clinical data associate jobs
- Exposure to global clinical trial processes
- Work on oncology, autoimmune, and neurological research domains
- Develop expertise in drug safety and data handling
- Build a foundation for careers in:
- Clinical Data Management
- Pharmacovigilance
- Medical Writing
- Regulatory Affairs
📥 How to Apply
