Clinical Data Services Associate – Life Sciences R&D | Bengaluru, India (Full-Time)
Experience Required: 0–2 years | Qualification: BE
Company Overview
Accenture is a global leader in professional services, delivering innovative solutions across digital, cloud, and security domains. Serving clients in over 120 countries, we combine technology and human ingenuity to help businesses transform and thrive. Within Life Sciences, Accenture partners with leading biopharma organizations to optimize clinical development, regulatory compliance, pharmacovigilance, and patient-focused services. Learn more at www.accenture.com.
Role Overview
The Clinical Data Services Associate will be part of the Clinical Data Management (CDM) team within the Life Sciences R&D vertical. You will support clinical trials by managing, reviewing, and validating clinical data, ensuring accuracy, completeness, and compliance with regulatory standards. This is an entry-level to early-career role ideal for candidates seeking exposure to global clinical research and data management operations.
Key Responsibilities
Clinical Data Management:
Perform data management activities including discrepancy review, query generation, and resolution.
Assist in creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines.
Identify protocol deviations in clinical databases and escalate as required.
Support edit check validation by preparing test cases and test scripts.
Assist in database validation (UAT) against specified CRF/eCRF.
Develop and review edit checks, patient profile listings, reports, preprocessing checks, and map datasets for validation based on study requirements.
Collaboration & Stakeholder Support:
Work closely with team members and supervisors to execute daily tasks effectively.
Support clinical data management projects, ensuring adherence to quality standards and timelines.
Contribute to the documentation of processes and findings for audits and compliance purposes.
Tools & Systems:
Gain experience with clinical data management tools and systems such as SAS, Cognos, J-Review, or equivalent platforms.
Candidate Profile
Educational Qualification:
Bachelor of Engineering (BE) in any relevant discipline.
Experience:
Freshers or candidates with 0–2 years of experience in clinical data management, clinical research, or related fields.
Skills & Competencies:
Adaptable and detail-oriented with strong problem-solving abilities.
Good understanding of clinical trial processes and electronic data capture (EDC) systems.
Strong communication and teamwork skills.
Ability to manage tasks independently while following SOPs and study protocols.
Flexibility to work in rotational shifts, if required.
Why Join Accenture
Work at the forefront of clinical data management in Life Sciences supporting global biopharma clients.
Gain exposure to end-to-end clinical trial operations and regulatory compliance.
Access to continuous learning, skill development, and certifications to advance your career.
Be part of a diverse and inclusive workplace fostering innovation, collaboration, and career growth.
Contribute to projects that improve patient outcomes worldwide.
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