Life Sciences Job at Accenture | Clinical Data Services Associate | Apply Now
Accenture is currently inviting applications for the position of Clinical Data Services Associate within its Life Sciences R&D vertical in Hyderabad. This Life Sciences Job is a specialized role focused on Clinical eTMF (Electronic Trial Master File) Management, ensuring the integrity and regulatory compliance of documentation throughout the clinical trial lifecycle. If you are a graduate seeking a structured Accenture Career that facilitates the delivery of high-quality data to global biopharmaceutical companies, this professional opportunity provides an ideal platform.
- Job Position: Clinical Data Services Associate
- Location: Hyderabad, Telangana, India.
- Job Identification: AIOC-S01629184
About the Company
Accenture is a leading global professional services organization with significant capabilities in digital, cloud, and security. With a workforce of 784,000 employees serving clients in over 120 countries, the company leverages advanced technology and human ingenuity to create shared success. A career within Accenture’s Life Sciences R&D vertical involves supporting the entire enterprise—from research laboratories and clinical trials to pharmacovigilance and regulatory services—helping biopharma companies improve patient outcomes through scientific expertise.
Key Responsibilities
The Clinical Data Associate role is centered on the management and processing of data collected during clinical trials. This process is essential for regulatory compliance and successful trial outcomes.
- TMF Analysis: Analysts work under the guidance of TMF Managers to perform data review and accuracy checks of Trial Master File tables of contents.
- Regulatory Documentation: Manage initial full protocol packages, amended FPP checklists, and end-of-trial checklists.
- Data Reconciliation: Ensure essential document reconciliation and the accurate compilation of clinical study report appendices.
- Lifecycle Management: Utilize specialized software and strategies to manage regulated content across the entire lifecycle of a clinical trial.
- Operational Excellence: Support the validation, storage, and analysis of data to evaluate the safety and efficacy of medical treatments.
Qualifications and Requirements
Accenture is seeking disciplined professionals with a strong background in science and data management.
- Education: A Bachelor of Science (BSc) degree is mandatory.
- Experience: 1 to 3 years of experience in clinical data services or a related function.
- Core Skills: Proficiency in Clinical eTMF Management and familiarity with clinical trial regulated content.
- Competencies:
- Ability to establish and maintain strong client relationships.
- Competence in managing multiple stakeholders and handling disputes professionally.
- Proven ability to meet strict deadlines and perform effectively under pressure.
Applying for the Clinical Data Services Associate position at Accenture Hyderabad is a significant step for professionals aiming to specialize in the operational and regulatory aspects of clinical research. This Life Sciences Job offers exposure to complex data management systems and the opportunity to work within a globally recognized R&D framework. By ensuring the accuracy of the Trial Master File, you will play a critical role in the development of safe and effective medical treatments.
