Senior Associate, Data Manager, Clinical Data Sciences
Location: India – Chennai
Job Type: Full-Time
Experience Required: 3–6 Years
Work Mode: On-Premise
Job ID: 4952888
Overview
An exciting opportunity is available for a Senior Associate, Data Manager within Clinical Data Sciences. This role is part of the Clinical Data and Information Sciences (CDIS) function, a critical unit supporting clinical development and operations. The position focuses on ensuring high-quality clinical data management, integrity, and compliance across clinical trials, contributing directly to the successful delivery of clinical programs.
Key Responsibilities
You will act as a Data Manager for one or more clinical trials with minimal supervision, taking ownership of end-to-end clinical data management activities. This includes the selection and implementation of data acquisition standards, database design, and the development and maintenance of Data Management Plans.
The role involves configuring and testing clinical data collection tools such as Case Report Forms (CRFs) and non-CRF systems using Electronic Data Capture (EDC) platforms. You will be responsible for data review, query management, and ensuring data accuracy, consistency, and completeness throughout the study lifecycle.
You will collaborate closely with Clinical Data Scientists to drive operational excellence and ensure alignment across all CDIS deliverables. Responsibilities also include managing data cleaning, e-data processing, data visualization, and reporting of data management metrics.
Additionally, you will oversee database release activities and contribute to submission readiness by ensuring all study-related documentation in the Trial Master File (TMF) is accurate, complete, and audit-ready. All activities must be conducted in compliance with applicable standard operating procedures and regulatory requirements.
Educational Qualifications
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Clinical Research, or a related field.
Experience Requirements
3 to 6 years of experience in clinical data management within the pharmaceutical, biotechnology, or CRO industry.
Required Skills and Competencies
Strong expertise in clinical data management processes and clinical trial workflows
Hands-on experience with EDC systems and clinical database design
Proficiency in data review, query management, and data cleaning processes
Familiarity with CDISC standards and clinical data regulations
Understanding of Trial Master File (TMF) processes and documentation requirements
Strong analytical, problem-solving, and organizational skills
Excellent communication and collaboration abilities
Ability to manage multiple studies and deliver within timelines
Why Join
This role offers the opportunity to work in a high-impact clinical data environment, contributing to global clinical trials and regulatory submissions. You will gain exposure to advanced data management systems, cross-functional collaboration, and global clinical development processes, enabling strong career growth in clinical data sciences.
Uttar Pradesh :
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