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Are you searching for high-growth Life science Jobs in the clinical trials industry? Here’s a powerful opportunity under Thermo Fisher Career for the position of CRA I (Immediate Joiners). If you are aiming to build a long-term career in clinical research associate jobs, this fully remote role allows you to work at the forefront of global clinical innovation while ensuring regulatory compliance and patient safety.
- Job Title: CRA I
- Location: Remote, India
- Job Id: R-01342870
- Job Type: Full-time
About the Company
Thermo Fisher Scientific is a global leader in serving science with a mission to make the world healthier, cleaner, and safer. Through its PPD clinical research portfolio, the company operates as a leading Contract Research Organization (CRO), supporting pharmaceutical and biotech companies worldwide. With operations across 100+ countries and thousands of clinical trials managed globally, Thermo Fisher delivers high-quality clinical monitoring and regulatory expertise.
Key Responsibilities
- Conduct risk-based monitoring using root cause analysis (RCA)
- Perform SDR, SDV, and CRF review for data accuracy
- Assess investigational product inventory and records
- Ensure protocol, ICH-GCP, and regulatory compliance
- Prepare monitoring reports and escalate issues to management
- Initiate, monitor, and close out clinical trial sites
- Maintain essential documents as per regulatory standards
- Provide trial status tracking and progress reports
- Facilitate communication between sites, sponsors, and project teams
- Ensure audit readiness and regulatory inspection support
Education and Experience Requirements
- Bachelor’s degree in a life sciences related field.
- Minimal clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years) in a clinical environment where experience is gained in clinical trials, medical terminology, medical research, clinical research or health care or experience in a health sciences field with formal training in medical terminology and anatomy may be considered.
- Valid driver’s license where applicable.
Skills Required
- Strong understanding of ICH-GCP guidelines
- Knowledge of clinical trials processes
- Critical thinking and problem-solving skills
- Good organizational and time management skills
- Strong written and oral communication skills
- Ability to manage Risk Based Monitoring concepts
- Proficiency in Microsoft Office and clinical systems
If you are aiming for impactful Life science Jobs, this CRA I opportunity under thermo Fisher Career offers global exposure, remote flexibility, and hands-on experience in clinical trials. For professionals seeking stable and growth-oriented clinical research associate jobs, this is your chance to work with one of the world’s leading CRO organizations.
