Assoc Clin Data Team Lead

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

ACDTL:

Join Us as a Clinical Data Associate I – Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 Bio-techs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

Role Overview:

As an Associate Clinical Data Team Lead, you will Acts as the assistant lead data manager for one or more projects supporting the lead data manager by performing assigned tasks in study set up, data cleaning, database close-out and other associated tasks.

What You’ll Do:

 Applies relevant components of the project protocol to daily tasks with guidance.

 Delivers study specific training to junior associates for assigned projects.

 Coordinates data cleaning tasks and delegates to appropriate data management

staff to ensure quality standards are maintained and project deliverable timelines

are met with minimal supervision.

 Assists with specified activities that contribute to the creation of database

specifications, database build and user acceptance testing during database and

edit check development.

 Monitors for risks to deadlines and escalates appropriately.

 Creates and maintains data management project documentation.

 Participates in team and client meetings and supports the lead data manager

with risk management on allocated projects.

 Provides input into project forecasting of hours and identification of resource

 Monitors study metrics and runs project-specific status reports for management.

 Reviews data management deliverables for allocated projects following

documented guidelines.

 Produces project-specific status reports for management, PM and/or clients on a

regular basis..

Education and Experience Requirements:

• Bachelor's degree or equivalent and relevant formal academic
• Previous experience (Min 3 to 4.6 Years) that provides the knowledge, skills, and abilities to perform the job
• Should have experience in RAVE / Veeva EDC

Knowledge, Skills and Abilities:

• Good written/ verbal communication skills with a strong command of English language and grammar; good organizational, analytical/problem solving skills and attention to detail
• Ability to apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, SOPs and client expectations
• Ability to work productively and minimal supervision
• Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
• Strong customer focus and excellent interpersonal skills
• Proven flexibility and adaptability
• Ability to work in a team environment and independently as needed
• Ability to train and direct junior team members
• Ability to set and meet timelines or be able to recognize and schedule changes in response to project demands

Working Conditions and Environment:

• Work is performed in an office or clinical environment with exposure to electrical office equipment.
• Occasional drives to site locations. Potential Occasional travel required.

Your Career Growth:

We are hiring a team in India to support our FSP client - a large, globally recognized biopharmaceutical organization with a strong legacy in specialty medicines, vaccines, and scientific innovation. This sponsor is known for its commitment to patients, global research and development, and long-term investment in science. As a client dedicated FSP employee, you will collaborate with our client’s global data science team, contribute to complex and high visibility initiatives, and work within a mature FSP delivery model focused on quality and partnership.

Our FSP model supports continuous learning and career development by offering employees tailored learning pathways, stretch assignments, and mentorship – this allows FSP professionals to expand their horizons. This role opens multiple career paths. You could progress along the Clinical Data Management track (e.g., Senior CDM, CDTL, CDM PM) or transition into Data Standards/Programming, based on skill, impact, and business need.

Why You’ll Want to Join:

• Join our FSP Data Management team and help bring life‑changing medicines to patients worldwide. Accelerate your growth with hands‑on experience in modern CDM, from EDC and data quality to AI‑enabled workflows—building the expertise to lead data‑driven study delivery in a rapidly evolving clinical landscape
• Global exposure:

Work on international clinical studies across phases and therapeutic areas, partner with global teams, CROs, vendors, and country operations.

• End-to-end ownership:

Contribute to every stage of study delivery, from set-up to close-out.

• Analytical & project skills:

Strengthen global project management, financial tracking, data analysis, and risk management abilities. Learn new clinical trial technologies like AI platforms to conduct a global clinical tria

About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, improving patient diagnostics and therapies or making their laboratory work more efficient, we are here to support them. Our distributed team of more than 90,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit www.thermofisher.com. Thermo Fisher Scientific is a Equal employment opportunity

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