Thermo Fisher Scientific Hiring Clinical Research Associates in India for clinical monitoring roles.
Company Overview
Thermo Fisher Scientific is a globally recognized life sciences organization supporting scientific discovery, healthcare innovation, and clinical research worldwide. Through its advanced research solutions and global clinical capabilities, the company plays a critical role in improving patient outcomes and accelerating the development of new therapies. Hiring Clinical Research Associates
As part of its clinical research ecosystem, Thermo Fisher Scientific delivers end-to-end clinical trial services across diverse therapeutic areas. With a strong focus on quality, compliance, and innovation, the organization provides professionals with the opportunity to work on impactful global studies while building long-term careers in clinical research.
Job Location & Employment Type
- Job Location: India (Onsite role with site visits; position tagged as remote in system)
- Employment Type: Full-time, permanent
- Work Schedule: Monday to Friday (Standard working hours)
- Functional Area: Clinical Operations / Clinical Research
Open Positions / Department Details
Thermo Fisher Scientific is hiring Clinical Research Associates (CRA) across multiple experience levels within its Clinical Operations team, supporting studies managed through its global clinical research services portfolio. Hiring Clinical Research Associates
Available Levels:
- Clinical Research Associate – Level I
- Clinical Research Associate – Level II
- Senior Clinical Research Associate
These roles involve direct responsibility for site monitoring, regulatory compliance, and trial oversight across assigned clinical studies.
Key Roles & Responsibilities
Clinical Research Associates will be responsible for ensuring that clinical trials are conducted in compliance with approved protocols, regulatory requirements, and international quality standards. Hiring Clinical Research Associates
Core Responsibilities Include:
- Managing and executing all clinical monitoring activities from site initiation to study close-out
- Conducting on-site and remote monitoring visits as per the monitoring plan
- Ensuring investigator sites comply with study protocols, SOPs, ICH-GCP guidelines, and applicable regulations
- Performing source data review (SDR), source data verification (SDV), and CRF review to ensure data accuracy
- Reviewing investigational product accountability through physical inventory checks and documentation review
- Identifying site-level issues, deviations, and risks, and ensuring timely resolution through corrective and preventive actions
- Applying risk-based monitoring principles, root cause analysis, and critical thinking to reduce compliance risks
- Preparing monitoring visit reports, follow-up letters, and documentation within defined timelines
- Maintaining regular communication with investigator sites between monitoring visits
- Supporting investigator payments and site management activities
- Ensuring essential trial documents are complete and audit-ready at all times
- Updating study systems such as Clinical Trial Management Systems (CTMS) as per project requirements
- Participating in investigator meetings, site selection activities, and feasibility assessments when required
- Supporting site initiation, interim monitoring, and study close-out activities
- Coordinating effectively with Clinical Team Managers (CTMs), project teams, sponsors, and internal stakeholders
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences or a related discipline
- Nursing qualification (Registered Nurse) or equivalent clinical education
- Relevant academic or vocational qualification related to clinical research
Experience
- Minimum 2+ years of experience as an on-site Clinical Research Monitor
- Experience across investigator site monitoring, regulatory compliance, and trial documentation
- Experience level will determine eligibility for CRA I, CRA II, or Senior CRA designation
- Valid driving license may be required depending on site travel needs
Equivalent combinations of education, training, and relevant experience may be considered. Hiring Clinical Research Associates
Skills Required
- Strong understanding of clinical monitoring processes and site management
- Practical knowledge of ICH-GCP guidelines, regulatory requirements, and clinical SOPs
- Familiarity with risk-based monitoring methodologies
- Ability to conduct root cause analysis and manage corrective actions
- Strong attention to detail with a focus on data quality and patient safety
- Excellent written and verbal communication skills in English
- Ability to interact professionally with investigators, site staff, and sponsors
- Good organizational, time-management, and documentation skills
- Ability to work independently while contributing effectively within project teams
- Proficiency in Microsoft Office and ability to learn clinical trial software systems
Salary & Benefits
Salary: As per company norms and based on experience, level, and project requirements Hiring Clinical Research Associates
Employee Benefits May Include (as per policy):
- Competitive compensation structure
- Health and wellness support programs
- Professional development and training opportunities
- Exposure to global clinical trials and multinational clients
- Structured career progression within clinical research operations
Selection Process
The selection process generally includes:
- Resume shortlisting based on eligibility and monitoring experience
- Technical interview with Clinical Operations leadership
- Final HR discussion and role alignment
Only shortlisted candidates will be contacted for further steps.
How to Apply
Interested candidates can apply online through the official Thermo Fisher Scientific careers portal using the job requisition ID. Hiring Clinical Research Associates
- Job Requisition ID: R-01326248
- Mode of Application: Online application only
Ensure your resume highlights relevant clinical monitoring experience and therapeutic area exposure.
Important Dates
- Last Date to Apply: Not specified (early application recommended)
Why Apply for This Pharma Job?
This opportunity is ideal for Clinical Research Associates seeking exposure to global clinical trials within a structured and quality-driven environment. Working with Thermo Fisher Scientific allows professionals to contribute to meaningful research that directly impacts patient health worldwide. The role provides hands-on involvement across the full clinical trial lifecycle, collaboration with international teams, and long-term growth within clinical operations. For CRAs aiming to strengthen their monitoring expertise while working on diverse therapeutic programs, this position offers strong professional value. Hiring Clinical Research Associates
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent pharmaceutical and clinical research job information platform. We are not affiliated with Thermo Fisher Scientific, its subsidiaries, or recruitment partners. Job details are shared for informational purposes only. Candidates should verify information independently and never pay any fees for recruitment or job applications. Hiring Clinical Research Associates
Final Call-to-Action
Clinical Research professionals with monitoring experience are encouraged to apply promptly and advance their careers in global clinical research. Hiring Clinical Research Associates
