Clinical Research Associate (CRA) – Level II
Location: Remote, India
Work Mode: Fully Remote
Job Type: Full-Time
Category: Clinical Research
Job ID: R-01331413
Work Schedule: Monday to Friday (Standard Business Hours)
Job Overview
Thermo Fisher Scientific is hiring an experienced Clinical Research Associate (CRA) – Level II to support global clinical trials within its PPD® Clinical Research Services portfolio. This role is ideal for clinical research professionals with strong on-site monitoring experience who are ready to take ownership of complex studies and ensure regulatory compliance, data integrity, and operational excellence.
As part of a leading global Contract Research Organization (CRO), you will contribute to advancing innovative therapies that address critical global health challenges.
Key Responsibilities
Coordinate and lead all aspects of assigned clinical trials to ensure data quality, subject safety, and regulatory compliance.
Perform and oversee on-site monitoring activities, including site initiation, routine monitoring, and close-out visits.
Collaborate with cross-functional teams to implement study protocols and achieve key project milestones.
Monitor study progress, timelines, and deliverables, ensuring adherence to project plans.
Maintain accurate, complete, and inspection-ready trial master file (TMF) and site documentation.
Ensure strict compliance with ICH-GCP, Indian regulatory requirements, sponsor SOPs, and company guidelines.
Identify, escalate, and support resolution of study risks, deviations, and issues.
Contribute to continuous process improvement and best practices in clinical operations.
Experience Requirements
Minimum 3 years of proven experience as a Clinical Research Associate, with hands-on on-site monitoring responsibilities.
Experience working on interventional clinical trials across one or more therapeutic areas is preferred.
Educational Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related discipline.
Advanced certifications in clinical research are an added advantage.
Required Skills & Competencies
Strong knowledge of ICH-GCP, Indian regulatory guidelines, and clinical trial processes.
Excellent organizational and time management skills with the ability to manage multiple studies.
Strong analytical and problem-solving abilities.
Ability to prioritize tasks and meet deadlines in a fast-paced environment.
Excellent written and verbal communication skills.
Proven ability to work independently while collaborating effectively with global teams.
High level of motivation, accountability, and attention to detail.
Location Flexibility
While the role is fully remote, candidates should be based in or willing to operate from major metro cities, including:
Mumbai, Delhi NCR, Bengaluru, Hyderabad, or Ahmedabad, to support site monitoring and travel requirements.
Why Join Thermo Fisher Scientific
Work with a world-class global CRO at the forefront of clinical research innovation.
Gain exposure to complex, multinational clinical trials.
Be part of a collaborative, inclusive, and performance-driven culture.
Access structured career development opportunities and long-term growth pathways in clinical research.
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, enabling customers to make the world healthier, cleaner, and safer. With a global workforce of more than 90,000 professionals, the company delivers innovative technologies, pharmaceutical services, and clinical research solutions across the life sciences industry.
Thermo Fisher Scientific is an Equal Employment Opportunity Employer, committed to diversity, equity, and inclusion.
Apply Now
If you are an experienced Clinical Research Associate passionate about advancing science and improving patient outcomes, apply now and be part of Thermo Fisher Scientific’s mission to drive clinical innovation globally.a
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Frank Scottile Blvd |Missouri :
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