Associate Clinical Data Team Lead (ACDTL) – Remote, India
Job ID: R-01338261
Location: Remote, India
Job Type: Full-Time
Category: Clinical Research / Clinical Data Management
Work Mode: Fully Remote
Work Schedule: Standard (Monday to Friday)
About the Role
We are seeking a highly motivated Associate Clinical Data Team Lead (ACDTL) to join our global Clinical Research Services team. This role supports high-impact clinical trials conducted for leading pharmaceutical and biotechnology organizations worldwide. As part of a global Contract Research Organization (CRO) supporting the PPD® clinical research portfolio, you will contribute directly to delivering high-quality clinical data that accelerates the development of life-changing therapies.
The Associate Clinical Data Team Lead acts as an assistant lead data manager on one or more clinical studies, supporting the Lead Data Manager across study start-up, data cleaning, database lock, and close-out activities while ensuring compliance with regulatory standards, SOPs, and project timelines.
Key Responsibilities
Support the Lead Data Manager in end-to-end clinical data management activities across assigned studies
Apply protocol requirements to daily data management tasks with appropriate guidance
Coordinate and oversee data cleaning activities, delegating tasks to data management team members while maintaining quality and timelines
Deliver study-specific training to junior clinical data associates
Assist in database specifications, database build activities, edit check development, and user acceptance testing (UAT)
Monitor project timelines, identify risks, and escalate issues proactively
Create, maintain, and review clinical data management documentation in compliance with SOPs and regulatory guidelines
Review data management deliverables to ensure accuracy, completeness, and adherence to documented standards
Prepare and distribute project-specific status reports for management, project managers, and clients
Monitor study metrics, support project forecasting, and assist with resource planning
Participate in internal and client meetings, contributing to risk management and operational excellence
Education and Experience Requirements
Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related scientific discipline (or equivalent formal qualification)
Minimum 3 to 4.6 years of relevant clinical data management experience
Proven experience working with RAVE and/or Veeva EDC systems
Prior experience in the pharmaceutical, biotechnology, or CRO industry preferred
Required Skills and Competencies
Strong written and verbal communication skills with excellent command of the English language
High attention to detail with strong organizational and analytical skills
Solid understanding of clinical data management processes, regulatory requirements, and SOPs
Ability to work independently with minimal supervision while managing multiple priorities
Demonstrated ability to train, guide, and coordinate junior team members
Strong problem-solving skills and proactive risk management approach
High standards of confidentiality and data integrity
Customer-focused mindset with strong interpersonal and stakeholder management skills
Flexibility and adaptability in a fast-paced, global project environment
Working Conditions
Work performed remotely or in an office-based clinical environment
Occasional travel to clinical sites or client locations may be required
Career Growth and Development
This role supports a Functional Service Provider (FSP) engagement with a globally recognized biopharmaceutical sponsor known for innovation in specialty medicines, vaccines, and advanced research. As an FSP-dedicated professional, you will collaborate closely with global data science and clinical teams on high-visibility studies.
The FSP delivery model emphasizes long-term partnership, quality, and professional growth. Employees benefit from structured learning pathways, mentorship, and stretch assignments. Career progression opportunities include advancement within Clinical Data Management (Senior CDM, CDTL, CDM Project Manager) or transitions into Data Standards, Programming, or related domains based on performance and business needs.
Why Join This Opportunity
Contribute to global clinical trials that bring life-changing therapies to patients worldwide
Gain hands-on exposure to modern clinical data management practices, including EDC, data quality oversight, and emerging AI-enabled workflows
Work on international, multi-phase studies across diverse therapeutic areas
Develop strong project management, analytical, and risk management capabilities
Collaborate with global stakeholders, CRO partners, vendors, and cross-functional teams
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding USD 44 billion. The company’s mission is to enable customers to make the world healthier, cleaner, and safer. With more than 90,000 colleagues globally, Thermo Fisher Scientific delivers innovative technologies, pharmaceutical services, and industry-leading solutions through trusted brands including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, and Patheon.
Thermo Fisher Scientific is an equal opportunity employer and is committed to fostering an inclusive and diverse workforce.
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