Remote Clinical Research Associate Hiring at Thermo Fisher
- Clinical Research Associate Openings for Life Science Graduates | Remote India
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Education
- Experience
- Skills & Competencies
- Location & Salary
- Location
- Work Environment
- Application Process
- FAQs
- 1. Who can apply for the CRA roles?
- 2. Is this a remote position?
- 3. What skills are required for a CRA position?
- 4. Does Thermo Fisher accept candidates from biotech or nursing backgrounds?
- 5. How do I apply?
- Summary Table
Clinical Research Associate Openings for Life Science Graduates | Remote India
Apply for CRA Level I–Sr CRA roles for BSc, MSc, BPharm graduates. Remote India positions with Thermo Fisher Scientific.
Thermo Fisher Scientific is hiring Clinical Research Associates (CRA Level I, Level II and Senior CRA) for its clinical operations team in India. These remote full-time openings are suited for candidates with hands-on clinical monitoring experience and a solid background in life sciences or nursing. This role supports global clinical trials across therapeutic areas, helping advance drug development with accuracy, compliance, and high scientific standards.
Company Overview
Thermo Fisher Scientific is a global leader in scientific research, laboratory solutions, and clinical development services. Through its PPD clinical research portfolio, the company supports studies in more than 100 countries and provides end-to-end clinical trial services. The organization is known for its strong commitment to scientific integrity, patient safety, and regulatory compliance. Professionals working here contribute to the development of life-changing therapies and the improvement of health outcomes worldwide.
Job Role & Responsibilities
As a Clinical Research Associate, you will manage clinical monitoring and site oversight activities to ensure trial compliance, data accuracy and audit readiness.
Key Responsibilities
- Conduct on-site and remote monitoring visits following ICH-GCP, study protocol and regulatory requirements.
- Use risk-based monitoring, root cause analysis and critical thinking to identify site issues and corrective actions.
- Verify source data through SDR, SDV and CRF checks.
- Review investigational product accountability, documentation and regulatory files.
- Prepare monitoring reports, follow-up letters and site communication in line with business writing standards.
- Escalate compliance issues to clinical management and track resolutions.
- Maintain ongoing communication with investigative sites to ensure adherence to study timelines.
- Participate in site initiation, close-out visits, and investigator meetings.
- Track study progress and update systems such as CTMS.
- Support investigator payments and documentation workflows.
- Ensure essential documents are complete and audit-ready.
- Collaborate with cross-functional teams to resolve operational challenges.
- Handle administrative tasks such as expense submission and timesheets.
Eligibility / Qualifications
Education
- Bachelor’s degree in a life science field (BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Life Sciences) or equivalent.
- BPharm, MPharm, MSc Life Sciences, or Registered Nursing certification also accepted.
Experience
- Minimum 2+ years of onsite clinical monitoring experience.
- Strong working knowledge of ICH-GCP and clinical research regulations.
Skills & Competencies
- Proven clinical monitoring ability.
- Solid understanding of medical terminology and therapeutic areas.
- Strong communication and documentation skills.
- High attention to detail and accuracy.
- Organizational and time-management strength.
- Ability to work independently and within cross-functional teams.
- Proficiency in Microsoft Office and willingness to learn new software.
Location & Salary
Location
- Remote, India (Full-time, standard Monday–Friday schedule).
Work Environment
- Office-based remote structure.
- Requires regular communication with diverse groups.
- Includes independent travel for monitoring visits.
- Exposure to healthcare or laboratory environments may occur.
- Must work efficiently under pressure while managing multiple priorities.
Application Process
Eligible candidates can apply directly via the company career portal. Ensure your resume highlights clinical monitoring experience, therapeutic exposure and familiarity with ICH-GCP.
Apply Here: https://jobs.thermofisher.com/global/en/job/R-01326248/CRA-Level-I-Level-II-and-Sr-CRA
FAQs
1. Who can apply for the CRA roles?
Candidates with BSc, MSc, BPharm, MPharm, Nursing or equivalent life science qualifications with at least 2 years of monitoring experience.
2. Is this a remote position?
Yes. The role is fully remote within India but involves travel for site visits.
3. What skills are required for a CRA position?
Strong knowledge of ICH-GCP, communication skills, risk-based monitoring, document accuracy and site management capabilities.
4. Does Thermo Fisher accept candidates from biotech or nursing backgrounds?
Yes. Biotechnology, Microbiology, Nursing, Pharmacy and Life Science graduates are eligible.
5. How do I apply?
Submit your application through the official Thermo Fisher job link provided above.
Summary Table
| Category | Details |
|---|---|
| Company | Thermo Fisher Scientific |
| Vacancies | CRA Level I, Level II, Senior CRA |
| Required Education | BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Life Sciences, BPharm, MPharm, MSc Life Sciences, Nursing certification |
| Experience | Minimum 2+ years of onsite clinical monitoring experience |
To apply for this job please visit jobs.thermofisher.com.
