Associate Clinical Data Manager
About the Role
We are seeking a motivated and detail-oriented Associate Clinical Data Manager to join our Clinical Data Management (CDM) team. This is an entry-level position ideal for candidates looking to start a long-term career in clinical research and data management. In this role, you will assist with the oversight and coordination of data collection, cleaning, and quality review activities for clinical trials.
You will work under the guidance of experienced Data Managers to ensure the accuracy, completeness, and integrity of clinical trial data in compliance with regulatory guidelines and study protocols.
Key Responsibilities
Assist in the development, testing, and validation of Electronic Data Capture (EDC) systems and Case Report Forms (CRFs)
Support database setup activities including edit check specifications and user acceptance testing (UAT)
Review incoming clinical data for completeness, consistency, and accuracy
Generate, track, and resolve data queries in collaboration with clinical sites
Maintain study documentation and data management files
Participate in cross-functional study team meetings and data review discussions
Support Serious Adverse Event (SAE) reconciliation and external data integration (e.g., labs, central imaging)
Ensure data management activities follow SOPs, study protocols, and regulatory standards (e.g., ICH-GCP, CDISC)
Qualifications
Required:
Bachelor’s degree in a life science, health science, pharmacy, public health, or related field
Strong attention to detail, organizational, and time management skills
Proficiency with Microsoft Office Suite (Excel, Word, PowerPoint)
Effective written and verbal communication skills
Ability to learn and apply technical systems and software (EDC, CTMS, etc.)
Preferred:
Internship or coursework experience in clinical research or data management
Familiarity with clinical trial processes and Good Clinical Practice (GCP)
Experience with EDC systems (e.g., Medidata Rave, Veeva Vault, Medrio) a plus