Clinical Data Management Job at Accenture | M Pharm Graduates | Apply Now
Looking for an M. Pharm Job in clinical research and life sciences? Accenture is hiring a Clinical Data Services Associate in Bengaluru. This opportunity is ideal for B. Pharm, M. Pharm graduates interested in clinical trials, medical monitoring, regulatory compliance, and healthcare data management while building a rewarding Accenture Career.
- Job Title: Clinical Data Services Associate
- Location: Bengaluru, Karnataka
About the Company
Accenture is a global professional services company with expertise in digital, cloud, technology, consulting, and operations. Operating in more than 120 countries with over 775,000 employees worldwide, Accenture helps organizations innovate and transform through technology and human ingenuity.
Within its Life Sciences R&D division, Accenture supports leading biopharmaceutical companies through clinical research, pharmacovigilance, regulatory services, patient services, and clinical trial operations, making it an excellent destination for professionals seeking an Accenture Career in healthcare and life sciences.
Job Description
The Clinical Data Services Associate will support clinical trial operations through data management, medical monitoring, protocol review, and clinical data validation activities. This M Pharm Job involves ensuring the accuracy, reliability, and regulatory compliance of clinical trial data while supporting pharmaceutical and biotechnology companies in evaluating the safety and effectiveness of medical treatments.
The role offers exposure to clinical research, regulatory services, pharmacovigilance, and life sciences operations, making it a valuable opportunity for professionals interested in healthcare data and clinical development.
Key Responsibilities
- Support clinical data collection, validation, processing, and analysis.
- Assist in medical monitoring and trial oversight activities.
- Review and validate protocol requirement specifications.
- Ensure data accuracy, consistency, and regulatory compliance.
- Follow applicable SOPs and clinical research guidelines.
- Resolve routine issues using established procedures and guidelines.
- Collaborate with team members and supervisors on assigned tasks.
- Support clinical trial data management activities.
- Contribute to safety monitoring and clinical research operations.
- Maintain documentation related to clinical studies and data services.
Qualification & Experience
- Education:
-
- Bachelor of Pharmacy (B. Pharm)
- Master of Pharmacy (M. Pharm)
Experience: Candidates with 1–3 years of relevant experience are preferred.
Required Skills
- Understanding of clinical research processes.
- Knowledge of clinical trial data management.
- Familiarity with medical monitoring activities.
- Awareness of regulatory and compliance requirements.
