Associate Clinical Data Team Lead (ACDTL) – Clinical Data Management
Location: Remote, India
Job Type: Full-Time
Category: Clinical Research / Data Management
Experience Required: 3 – 5 years in Clinical Data Management
Job Overview
We are seeking an Associate Clinical Data Team Lead (ACDTL) to support lead data managers in managing clinical data across one or more projects. This role focuses on study setup, data cleaning, database close-out, and quality deliverables. The ACDTL will coordinate junior team members, provide study-specific training, and ensure all CDM activities are completed efficiently, accurately, and in compliance with regulatory guidelines.
Key Responsibilities
Data Management Support
Assist lead data manager in end-to-end data management activities, including study setup, database build, edit checks, and data cleaning
Review project protocols and apply relevant components to daily CDM tasks
Monitor data quality, track project metrics, and escalate risks to the lead data manager
Ensure database specifications and eCRF updates are implemented accurately
Maintain and update project-specific CDM documentation
Team Coordination & Training
Deliver study-specific training to junior CDM associates
Delegate data cleaning tasks to team members and ensure timely completion of deliverables
Mentor junior associates and provide guidance to maintain quality standards
Project & Client Collaboration
Participate in team and client meetings, supporting lead data manager with study operations and risk management
Contribute to resource forecasting, project timelines, and identification of potential out-of-scope activities
Generate project-specific status reports for management and clients
Education & Experience
Education:
Bachelor’s degree or equivalent in Life Sciences, Pharmacy, or related field
Experience:
3 – 4.6 years of experience in clinical data management
Hands-on experience with RAVE / Veeva EDC
Skills & Competencies
Strong knowledge of clinical trial protocols, CDM processes, SOPs, and GCP guidelines
Excellent written and verbal communication skills in English
Ability to lead, train, and guide junior associates effectively
Strong organizational, analytical, and problem-solving skills
Attention to detail and commitment to data quality
Ability to work independently and collaboratively in a remote environment
Maintain confidentiality of clinical data and client proprietary information
Flexibility and adaptability to changing project demands
Career Growth & Global Exposure
Progression opportunities along the Clinical Data Management track (e.g., CDTL, Senior CDM, CDM PM)
Exposure to international clinical studies and cross-functional teams
Hands-on experience with modern CDM tools, EDC systems, and AI-enabled workflows
Develop expertise in inspection-ready datasets, data validation, and study metrics
Why Join
Global Impact: Contribute to studies delivering life-changing therapies worldwide
End-to-End Ownership: Engage in all stages of study delivery, from setup to database close-out
Professional Development: Mentorship, stretch assignments, and career growth opportunities
Innovation: Work with AI-enabled platforms and modern clinical trial technologies
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