Are you a Life Sciences graduate with 5-8 years of experience in clinical research? Tata Consultancy Services (TCS), a global leader in IT and consulting, is hiring for the role of Study Delivery Specialist (Clinical Research Associate) in Mumbai, Pune, and Bangalore. This is an excellent opportunity for professionals looking to advance their careers in clinical trial management, study operations, and project delivery within the pharmaceutical and healthcare domain.
Job Details:
- Position: Study Delivery Specialist (SDS) / Clinical Research Associate
- Location: Mumbai, Pune, Bangalore (On-site)
- Experience: 5-8 years in clinical research or study management
- Qualification: Any Life Sciences graduate
- Job Type: Full-time
- Posted: Recently (High applicant volume – Apply soon!)
Key Responsibilities:
As a Study Delivery Specialist at TCS, you will be responsible for:
1. Study Operational Activities
- Managing end-to-end clinical trial processes.
- Ensuring compliance with regulatory and protocol requirements.
- Coordinating with cross-functional teams for smooth study execution.
2. Trial Master File (TMF) Management
- Maintaining accurate and inspection-ready TMF documentation.
- Ensuring all study documents are filed and archived properly.
3. Study Budget Management
- Tracking study expenses and ensuring cost efficiency.
- Handling vendor payments and financial reconciliations.
4. Vendor and Contract Management
- Overseeing third-party vendors (CROs, labs, etc.).
- Managing contracts and service agreements.
5. System Data Accuracy
- Ensuring data integrity across clinical trial systems.
- Performing quality checks on study databases.
6. Quality Management
- Implementing quality control measures for study compliance.
- Supporting audits and corrective action plans.
Why Join TCS?
- Work with a global leader in IT and healthcare solutions.
- Career growth in clinical research and project management.
- Competitive salary and employee benefits.
- Collaborative work environment with industry experts.
Who Should Apply?
- Life Sciences graduates with 5+ years in clinical research, study management, or trial operations.
- Professionals experienced in TMF, budget tracking, vendor management, and regulatory compliance.
- Strong project management and communication skills.
How to Apply?
- Easy Apply option available – Submit your resume now!
- Tailor your resume to highlight clinical research and study management experience.
- Premium applicants can get AI-powered job-fit analysis.
