Roles & Responsibilities
• Support Clinical Data Services with a focus on Medical Monitoring activities
• Provide medical expertise for clinical trial oversight and safety evaluation
• Support data collection, validation, storage, and analysis during clinical trials
• Ensure clinical data accuracy, reliability, and regulatory compliance
• Create, review, and validate protocol requirement specifications as per applicable SOPs
• Assist in evaluating safety and efficacy data for ongoing clinical trials
• Solve routine clinical data issues using standard guidelines and established procedures
• Collaborate primarily with immediate team members and supervisors
• Follow detailed to moderate instructions for daily tasks and new assignments
• Ensure high-quality data outputs to support successful trial outcomes
• Work as an individual contributor within a defined scope of responsibilities
• Willingness to work in rotational shifts, as required
Qualification
• BE / Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm)
Experience
• 1–3 years of experience in:
– Clinical Data Services
– Clinical Data Management
– Medical Monitoring or clinical trial support roles
Skills
• Strong analytical and problem-solving skills
• Adaptable and flexible working style
• Ability to work under defined guidelines and processes
• Attention to detail and data accuracy
• Ability to work effectively as part of a team
About the Organisation
Accenture is a global professional services company with leading capabilities in digital, cloud, security, and life sciences. With over 699,000 professionals across 120+ countries, Accenture supports the entire life sciences value chain-from research and clinical trials to regulatory, pharmacovigilance, and patient services-helping biopharma companies deliver safe, effective treatments and improve patient outcomes worldwide.