Clinical Research Associate (CRA) – Level II
Location: Remote, India
Job ID: R-01331413
Employment Type: Full-time
Work Schedule: Standard (Monday–Friday)
Category: Clinical Research / Remote
About the Company
Thermo Fisher Scientific is a global leader in life sciences and clinical research solutions. Our Clinical Research Services (CRS) team drives the development of innovative therapies by ensuring the highest quality in clinical trial execution. As part of a leading Contract Research Organization (CRO), our professionals deliver scientific expertise and operational excellence to support life-changing drugs across therapeutic areas.
Joining Thermo Fisher Scientific means becoming part of a world-class, collaborative team where innovation, inclusion, and professional growth are at the forefront.
Role Overview
The Clinical Research Associate (CRA) – Level II will be responsible for the management, monitoring, and oversight of clinical trials across India. The role ensures compliance with regulatory requirements, Good Clinical Practice (GCP), and company standards, while maintaining data integrity and study quality. This position works closely with cross-functional teams to implement study protocols and achieve project milestones.
This is a fully remote role, with the expectation that candidates are based in major metro cities in India (Mumbai, Delhi NCR, Bengaluru, Hyderabad, Ahmedabad) for periodic on-site activities as required.
Key Responsibilities
Coordinate and oversee all aspects of clinical trial conduct to ensure adherence to study protocols, GCP, and regulatory requirements.
Conduct on-site monitoring visits, including source data verification, site management, and documentation review.
Collaborate with cross-functional teams including project managers, data managers, and medical monitors to ensure smooth study execution.
Track and report study progress, milestones, and deviations to ensure timely completion of deliverables.
Maintain accurate, complete, and up-to-date study documentation in accordance with company and regulatory standards.
Identify, report, and follow up on study-related issues, ensuring effective resolution and compliance.
Support site training and provide guidance to site staff on protocol requirements and study conduct.
Required Qualifications and Experience
Education
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or related scientific discipline.
Experience
Minimum 3 years of clinical research experience in on-site monitoring or CRA-level responsibilities.
Demonstrated experience with clinical trial management in India and knowledge of Indian regulatory requirements.
Strong understanding of Good Clinical Practices (GCP) and industry regulations.
Skills and Competencies
Excellent organizational and time management skills with the ability to manage multiple projects simultaneously.
Strong analytical, problem-solving, and decision-making skills.
Effective written and verbal communication skills in English, with the ability to collaborate with diverse teams.
Ability to prioritize tasks and meet deadlines in a fast-paced environment.
High degree of professionalism, attention to detail, and accountability.
Self-motivated, ambitious, and proactive in driving study success.
Work Environment and Benefits
Fully remote role with flexible work arrangements.
Opportunity to work on global clinical trials with cutting-edge therapies.
Exposure to professional development and career growth within a leading CRO.
Collaborative and inclusive work culture that values innovation, scientific excellence, and team engagement.
Apply Now
Advance your career in clinical research by joining Thermo Fisher Scientific. Contribute to high-impact studies, ensure patient safety, and help deliver life-changing therapies globally.
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Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Arizona | Buffalo Grove | Clayton | Downers Grove | fairmont | Georgia | Keene | Michigan | Mt. Pleasant | New Jersy | OH | Piedmont | Salisbury | United States | Whitesboro | Winston-Salem |Georgia :
Atlanta | Augusta | Rome |Maine :
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Detroit | Houghton Lake | Macomb | Southfield |North Dakota :
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Frank Scottile Blvd |Missouri :
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Copenhagen | Denmark |Europe :
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Istanbul | Turkey |Norway :
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Donegal |Meath :
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Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
Harrogate |South Yorkshire :
Sheffield |Oxfordshire :
Witney |Ontario :
Uxbridge | North York | Richmond Hill | Renfrew | Mississauga | Australia |Canada :
Canada |Quebec :
Montreal |Brussels :
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Argentina | Peru |Brazil :
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Croatia |Zagreb :
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Estonia | Tartu |Harju County (Maakond) :
Tallinn |Hà Nội :
Hà Nội | Hanoi |Ho Chi Minh :
Ho Chi Minh City |Italy :
Italy |Lombardy :
Rho |Jakarta :
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Japan | Saitama |Tokyo :
Otemachi |North Ostrobothnia :
Oulu |Southwest Finland (Varsinais-Suomi) :
Turku |Remote Korea :
Remote Korea |Republic of Korea :
Seoul |Kazakhstan :
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New Mexico | Ciudad de México |Dubai :
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Kyiv |Lima Region :
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South Africa | Midrand |Nišava District :
Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
Sarajevo |Singapore :
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Sofia |Sweden :
Sweden |Taipei :
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