Clinical Research Associate Jobs at Thermo Fisher Scientific in Mumbai for remote clinical research roles with onsite monitoring experience.
Job Type: Full Time
Work Mode: Fully Remote
Location: Mumbai, India
Experience Required: 1 – 1.5 Years
Education: B.Pharm, M.Pharm, Pharm.D, MSc, BSc Life Sciences
Industry: Clinical Research, CRO, Pharmaceuticals, Biotechnology
Application Mode: Online Application
About the Company
Thermo Fisher Scientific is a global leader in scientific research services, supporting pharmaceutical, biotechnology, and healthcare organizations worldwide. The company plays a critical role in advancing clinical research by enabling high-quality, compliant, and innovative clinical trials across multiple therapeutic areas. Clinical Research Associate Jobs at Thermo Fisher Scientific
Through its clinical research operations, Thermo Fisher Scientific has supported thousands of global studies, collaborating with leading pharmaceutical companies and biotechnology organizations across more than 100 countries.
Job Details
Job Title: Clinical Research Associate (CRA I / CRA II)
Company: Thermo Fisher Scientific
Employment Type: Full Time
Work Model: Fully Remote
Base Location: Mumbai, India
Travel Requirement: Up to 60–75% (as per monitoring plan)
Experience Level: CRA Level I / Level II
Job Description
Thermo Fisher Scientific is hiring Clinical Research Associates (CRA I / CRA II) for a fully remote role based in Mumbai. This position is ideal for clinical research professionals with 1–1.5 years of on-site monitoring experience who want to work on global clinical trials while adhering to ICH-GCP and regulatory standards. Clinical Research Associate Jobs at Thermo Fisher Scientific
The CRA will be responsible for coordinating and overseeing clinical trial activities for assigned sites from start-up through close-out, ensuring subject safety, data integrity, and audit readiness. The role provides exposure to risk-based monitoring, advanced clinical systems, and collaboration with global sponsors and investigational sites. Clinical Research Associate Jobs at Thermo Fisher Scientific
Key Responsibilities
- Coordinate and oversee clinical trial activities from site initiation to close-out
- Conduct on-site and remote monitoring visits as per protocol and monitoring plans
- Perform risk-based monitoring activities, including SDV and SDR
- Review and manage clinical trial data using EDC, CTMS, IWRS, and eTMF systems
- Ensure trial conduct complies with ICH-GCP, SOPs, and applicable regulations
- Maintain audit readiness and support site audits and regulatory inspections
- Prepare and submit accurate monitoring visit reports and follow-up letters
- Track country-level metrics and proactively resolve site-level issues
- Communicate regularly with investigators and site staff regarding study status
- Support development and implementation of CAPAs
- Mentor and support junior CRA team members when required
- Travel to clinical sites as per monitoring plan requirements
- Complete administrative tasks such as timesheets and expense reports on time
Clinical Research Associate Jobs at Thermo Fisher Scientific
Skills / Qualifications
Educational Qualifications
- B.Pharm, M.Pharm, Pharm.D, MSc, or BSc in Life Sciences or related disciplines
Experience Requirements
- Minimum 1–1.5 years of on-site monitoring experience in clinical trials (mandatory)
- Experience working in an FSP model is preferred but not mandatory
- Valid driver’s license where applicable
Equivalent combinations of education, training, and relevant experience may be considered. Clinical Research Associate Jobs at Thermo Fisher Scientific
Required Skills & Competencies
- Strong knowledge of ICH-GCP guidelines and clinical research regulations
- Excellent understanding of clinical trial processes and medical terminology
- Proficiency in clinical systems such as CTMS, EDC, IWRS, and eTMF
- Strong documentation and data review skills
- Excellent verbal and written communication skills in English
- Ability to manage multiple trials and priorities simultaneously
- Strong problem-solving and risk management abilities
- Ability to work independently while collaborating with cross-functional teams
- Familiarity with Risk-Based Quality Management (RBQM) principles
- Digital literacy with Microsoft Office and clinical research software
Clinical Research Associate Jobs at Thermo Fisher Scientific
Benefits / Perks
- Fully remote working model with global exposure
- Opportunity to work on multinational clinical trials
- Structured onboarding, training, and mentoring programs
- Career progression from CRA I to CRA II and beyond
- Exposure to top pharmaceutical and biotechnology sponsors
- Competitive compensation and standard industry benefits
Clinical Research Associate Jobs at Thermo Fisher Scientific
Why You Should Join
- Work with a globally recognized life sciences organization
- Gain hands-on experience in complex, high-quality clinical trials
- Strengthen your career in clinical research and monitoring
- Collaborate with global teams and leading industry experts
- Long-term growth opportunities in clinical development
Clinical Research Associate Jobs at Thermo Fisher Scientific
Frequently Asked Questions (FAQs)
Is this a fully remote role?
Yes, the role is fully remote, with travel required for monitoring visits.
Is on-site monitoring experience mandatory?
Yes, 1–1.5 years of on-site monitoring experience is mandatory.
How much travel is expected?
Travel requirements may range between 60–75%, depending on study needs.
Is this role suitable for both CRA I and CRA II candidates?
Yes, the position is open to both CRA I and CRA II professionals.
Is FSP experience required?
FSP experience is preferred but not mandatory.
How to Apply
Interested and eligible candidates should apply through the official Thermo Fisher Scientific careers portal.
Only shortlisted candidates will be contacted for further stages of the selection process. Clinical Research Associate Jobs at Thermo Fisher Scientific
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