Clinical Research Associate (CRA) – Level II
Location: Remote, India
Job Type: Full-time
Experience Required: Minimum 3 years in clinical research (on-site monitoring)
About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in serving science, empowering life sciences and healthcare organizations to make the world healthier, cleaner, and safer. Our Clinical Research team drives innovation in drug development, collaborating with top pharmaceutical and biotechnology companies worldwide. As part of our global Contract Research Organization (CRO), you will contribute to clinical trials that transform patient care and advance medical science.
Role Overview
We are seeking a Clinical Research Associate (Level II) to coordinate and monitor clinical trials across diverse therapeutic areas. This role ensures regulatory compliance, data integrity, and timely execution of study protocols. The CRA II will collaborate with cross-functional teams and participate in projects that have high scientific and global impact.
Key Responsibilities
Coordinate, monitor, and manage clinical trials to ensure compliance with regulatory requirements and study protocols.
Conduct site visits, audits, and monitoring activities to ensure adherence to Good Clinical Practices (GCP).
Collaborate with cross-functional teams including Project Management, Data Management, and Clinical Operations to implement study protocols effectively.
Maintain accurate and detailed documentation of all trial activities in alignment with company SOPs and regulatory guidelines.
Identify and resolve study-related issues, reporting progress and deviations to project leads.
Ensure timely completion of deliverables while maintaining high-quality standards in clinical trial execution.
Required Qualifications & Experience
Minimum 3 years of clinical research experience with hands-on exposure to on-site monitoring.
Strong knowledge of Indian regulatory requirements and GCP guidelines.
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or related field.
Excellent organizational, time management, and multi-tasking skills.
Strong written and verbal communication skills to interact with study sites, sponsors, and internal teams.
Ability to prioritize tasks, meet deadlines, and manage multiple projects simultaneously.
Willingness to be based in a major metropolitan city (Mumbai, Delhi NCR, Bengaluru, Hyderabad, Ahmedabad).
Preferred Skills
Experience in cross-functional collaboration and global clinical trial operations.
Familiarity with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
Problem-solving mindset with a proactive approach to addressing site and study issues.
Why Join Thermo Fisher Scientific
Work on high-impact clinical trials that drive scientific innovation and improve patient outcomes.
Collaborate with a global, multidisciplinary team of clinical research professionals.
Gain exposure to cutting-edge technologies and global clinical trial practices.
Opportunities for professional development, career growth, and global exposure.
Apply Now
Join Thermo Fisher Scientific and contribute to life-changing clinical research. Help bring innovative therapies to patients worldwide while advancing your career in a supportive and inclusive environment.
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Siliguri |Illinois :
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Atlanta | Augusta | Rome |Maine :
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Frank Scottile Blvd |Missouri :
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Sheffield |Oxfordshire :
Witney |Ontario :
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Niš |Bohemia :
Prague |Chile :
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