Clinical Data Services Associate | Bengaluru, India | Full-Time
Location: Bengaluru, Karnataka, India
Experience Required: 0–2 years
Industry: Life Sciences / Clinical Data Management / R&D
Employment Type: Full-Time
About Accenture Life Sciences
Accenture is a global professional services leader, delivering innovative solutions in digital, cloud, and security. With specialized expertise across 40+ industries, we provide Strategy & Consulting, Technology & Operations, and Accenture Song services. With 784,000 professionals in over 120 countries, we combine technology and human ingenuity to help clients achieve measurable outcomes.
Within our Life Sciences R&D vertical, we support global biopharma companies across the clinical research lifecycle, from lab research, clinical trials, regulatory services, pharmacovigilance, to patient services.
Role Overview
The Clinical Data Services Associate will be responsible for managing and processing clinical trial data to ensure accuracy, reliability, and regulatory compliance. This role is essential to support the evaluation of safety and efficacy of medical treatments, enabling high-quality outcomes for clinical research.
You will work within a collaborative team environment, contributing to Clinical, Pharmacovigilance, and Regulatory projects. This role offers exposure to industry-leading processes and technologies in clinical data management.
Key Responsibilities
Collect, validate, and process clinical trial data accurately in line with project protocols.
Maintain high-quality standards for data entry, cleaning, and validation using specialized software systems.
Support integration and availability of data across studies, ensuring compliance with regulatory and NIH guidelines.
Resolve routine data management issues through standard procedures and escalation when needed.
Collaborate with team members and supervisors to ensure timely and precise completion of assignments.
Participate in quality control, reporting, and documentation activities.
Work in rotational shifts, if required, to meet project timelines.
Contribute to continuous improvement initiatives in data management processes.
Qualifications & Experience
Educational Background: Bachelor of Pharmacy (B.Pharm), Master of Pharmacy (M.Pharm), or Master’s in Actuarial Science.
Experience: 0–2 years of experience in clinical data management or related life sciences roles.
Skills Required:
Strong analytical and problem-solving skills.
Proficiency in English (Intermediate level) for domestic communication.
Attention to detail and commitment to data accuracy.
Ability to work effectively in a team environment.
Familiarity with clinical data management systems is a plus.
Why Join Accenture
Gain hands-on experience in clinical data services supporting global biopharma projects.
Exposure to advanced technologies and innovative clinical research processes.
Opportunity for career growth through contract conversion and skill development programs.
Be part of a diverse, collaborative, and inclusive workplace culture.
Competitive benefits and professional development opportunities within a global organization.
Accenture is an equal opportunity employer, committed to creating a workplace free from discrimination. All qualified applicants will receive consideration regardless of race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or veteran status. Reasonable accommodations are provided for qualified individuals with disabilities or for religious observances.
Apply now to join Accenture’s Life Sciences team and contribute to advancing global clinical research through high-quality data services.
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