CRA Job Opportunity at Thermo Fisher Scientific | Apply Now
Looking for a CRA job in a global life sciences company? Thermo Fisher Scientific is hiring a Clinical Research Associate (Level I) in Lisbon, Portugal. This exciting opportunity allows candidates to work at the forefront of clinical research, contributing to groundbreaking trials and supporting drug development worldwide. If you are aiming for Thermo Fisher careers, this role offers excellent exposure in clinical trials and global healthcare innovation.
- Job Position: Clinical Research Associate I (CRA Level I)
- Location: Lisbon, Portugal
- Job ID: R-01345625
- Job Type: Full-time
- Work Schedule: Standard Office Hours (40 hours/week)
About the Company
Thermo Fisher Scientific is a global leader in scientific research services and solutions. Through its PPD® clinical research portfolio, the company supports pharmaceutical and biotech organizations in bringing life-saving treatments to market. With experience across 2,700 clinical trials in over 100 countries, Thermo Fisher careers offer unmatched global exposure and innovation-driven opportunities in the life sciences sector.
Job Description
Join Thermo Fisher Scientific as a Clinical Research Associate I and become part of a high-impact clinical research team. This CRA job offers the opportunity to work on global clinical trials, ensuring compliance with protocols, regulatory standards, and ICH-GCP guidelines.
As part of leading Thermo Fisher careers, you will perform monitoring activities, manage site processes, and ensure data reliability. This life science job involves both remote and on-site monitoring, collaboration with investigational sites, and maintaining audit readiness.
Qualifications
- Bachelor’s degree in life sciences or related field
- Equivalent academic or vocational qualifications may be considered
- Valid driver’s license (if applicable)
Experience Required
- Minimum 2 years of clinical monitoring or relevant clinical research experience
- Experience in clinical trials, medical research, or healthcare environments
- Knowledge of medical terminology and anatomy
Skills and Competencies
- Strong understanding of ICH-GCP guidelines and regulatory requirements
- Excellent communication and interpersonal skills
- Strong problem-solving and critical thinking abilities
- Ability to manage risk-based monitoring processes
- Good organizational and time management skills
- Proficiency in Microsoft Office and clinical systems
- Ability to work independently and in teams
- Strong attention to detail and customer focus
- Good English language proficiency
Key Responsibilities
- Monitor investigator sites using a risk-based monitoring approach
- Perform root cause analysis (RCA) and implement corrective actions
- Ensure data accuracy through SDR, SDV, and CRF review
- Conduct on-site and remote monitoring visits
- Maintain documentation and ensure regulatory compliance
- Communicate effectively with investigative sites and internal teams
- Participate in investigator meetings and site selection processes
- Initiate, monitor, and close clinical trial sites
- Ensure essential documents are complete as per ICH-GCP guidelines
- Track trial progress and provide status updates
- Support audit readiness and regulatory inspections
- Contribute to project improvements and team collaboration
