Clinical Research Associate I Jobs in India Remote at Thermo Fisher Scientific | Apply Online with travel requirement.
IndiaPharmaJobs.in brings an exciting remote clinical research opportunity for experienced professionals looking to grow in the field of clinical monitoring. Thermo Fisher Scientific is inviting applications for the position of Clinical Research Associate I (CRA I) for candidates based in India. This role is ideal for professionals with prior monitoring experience who are ready to handle global clinical trials while working remotely with structured travel requirements.
If you have hands-on experience in site monitoring, knowledge of ICH-GCP guidelines, and strong documentation skills, this could be your next career advancement step in clinical research. Clinical Research Associate I Jobs in India
Company Overview
Thermo Fisher Scientific is a globally recognized organization serving the pharmaceutical, biotechnology, healthcare, and research industries. The company supports drug development programs, laboratory services, and clinical research operations worldwide. With operations across multiple countries, Thermo Fisher plays a crucial role in advancing scientific innovation and supporting clinical trials from early development to post-marketing phases.
Through its clinical research services division, the company collaborates with leading pharmaceutical and biotech firms to ensure regulatory compliance, patient safety, and high-quality data management throughout the clinical trial lifecycle. Clinical Research Associate I Jobs in India
Job Location & Employment Type
- Location: Remote (India-based candidates)
- Employment Type: Full-Time
- Work Schedule: Monday to Friday
- Travel Requirement: 60–80% travel including on-site visits and occasional overnight stays
- Requisition ID: R-01342870
This role offers work-from-home flexibility combined with significant field monitoring responsibilities across assigned clinical trial sites.
Open Position Details
- Position Title: Clinical Research Associate I (CRA I)
- Department: Clinical Operations / Clinical Monitoring
- Industry: Clinical Research / CRO Services
The CRA I will be responsible for overseeing clinical trial sites to ensure adherence to study protocols, regulatory requirements, and sponsor expectations. Clinical Research Associate I Jobs in India
Key Roles & Responsibilities
Clinical Trial Monitoring
- Conduct routine on-site and remote monitoring visits using risk-based monitoring methodologies.
- Perform Source Data Verification (SDV) and Source Data Review (SDR) to ensure data accuracy.
- Review Case Report Forms (CRFs) for completeness and protocol compliance.
- Identify and document protocol deviations and implement corrective and preventive actions.
- Ensure study conduct aligns with ICH-GCP guidelines and regulatory standards.
Site Initiation & Closeout Activities
- Support site initiation visits (SIV), interim monitoring visits, and close-out visits.
- Confirm investigator site files are complete and audit-ready.
- Ensure regulatory documents and essential study records are properly maintained.
- Coordinate with investigators and site staff for smooth study execution.
Risk Management & Compliance
- Apply root cause analysis (RCA) techniques to identify issues affecting study quality.
- Monitor investigational product accountability and storage conditions.
- Escalate compliance concerns to clinical management in a timely manner.
- Ensure subject safety and data integrity across assigned sites.
Documentation & Reporting
- Prepare comprehensive monitoring visit reports within defined timelines.
- Draft follow-up letters and action plans for site corrections.
- Update Clinical Trial Management System (CTMS) regularly.
- Assist with sponsor audits and regulatory inspections.
Stakeholder Communication
- Maintain regular communication with sponsors, investigators, and cross-functional teams.
- Collaborate with project managers, regulatory teams, and data management units.
- Support site payments and administrative coordination when required.
Clinical Research Associate I Jobs in India
Eligibility Criteria
Education
Candidates must possess one of the following qualifications:
- Bachelor’s degree in Pharmacy (B.Pharm)
- Master’s degree in Pharmacy (M.Pharm)
- Pharm.D
- B.Sc or M.Sc in Life Sciences
- Nursing (Registered Nurse – RN)
- Equivalent life science qualification
Experience
- Minimum 2 years of clinical monitoring experience is mandatory.
- Prior experience working in clinical trials, CROs, hospitals, or research environments preferred.
- Exposure to multi-center or global clinical trials will be advantageous.
Skills Required
- Strong knowledge of ICH-GCP guidelines and regulatory frameworks.
- Experience in Risk-Based Monitoring (RBM) approach.
- Sound understanding of clinical trial documentation processes.
- Proficiency in Microsoft Office tools (Word, Excel, PowerPoint).
- Excellent written and verbal English communication skills.
- Analytical mindset with problem-solving capabilities.
- Ability to manage frequent travel and site coordination responsibilities.
Clinical Research Associate I Jobs in India
Salary & Benefits
- Estimated Salary Range: ₹6,00,000 – ₹9,00,000 per annum (CTC)
- Compensation may vary based on experience level, therapeutic area exposure, and monitoring expertise.
- Additional benefits are offered as per company policies.
Selection Process
The hiring process may include:
- Application screening
- HR discussion
- Technical/functional interview
- Final managerial interview
- Offer release
Candidates shortlisted after application review will be contacted for further assessment. Clinical Research Associate I Jobs in India
How to Apply
Interested and eligible candidates must apply through the official online application portal of Thermo Fisher Scientific.
- Application Mode: Online Application
- Candidates should search using Requisition ID: R-01342870
Ensure that your resume highlights monitoring experience, therapeutic exposure, and compliance knowledge before submitting your application.
Important Dates
- Application Deadline: Not specified (Apply at the earliest to avoid missing the opportunity)
Why Apply for This Pharma Job?
- Opportunity to work with a globally respected clinical research organization.
- Exposure to international multi-country clinical trials.
- Remote working flexibility combined with structured monitoring operations.
- Strong compliance-oriented environment that enhances regulatory expertise.
- Career growth potential within clinical operations and project management pathways.
- Competitive salary package aligned with industry standards.
This position is ideal for professionals seeking stability, global exposure, and structured career progression within the clinical research industry. Clinical Research Associate I Jobs in India
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform that shares employment opportunities for the pharmaceutical and healthcare industry. We are not affiliated with Thermo Fisher Scientific or any other company mentioned above. Candidates are advised to apply only through the official company website and verify all job-related information independently. Clinical Research Associate I Jobs in India
Final Words
If you meet the eligibility criteria and have hands-on experience in clinical trial monitoring, do not miss this remote opportunity with a global leader in scientific services. Update your resume, highlight your monitoring expertise, and apply online as soon as possible to take the next step in your clinical research career. Clinical Research Associate I Jobs in India
