CRA I/II - FSP - Belgium **Attractive Sign On Bonus for starters by end of 2025*

About the Role

The FSP division at Thermo Fisher Scientific is a dynamic and rapidly growing area of the business, with a focus on delivering high-quality services to clients across the globe. As a CRA within this division, you will have the opportunity to work on a wide range of projects, from early-phase clinical trials to large-scale, multinational studies. You will be supported by a team of experienced professionals, including trainers, mentors, and technical experts, to ensure that you have the skills and knowledge needed to succeed in this role.

What You Will Do

• Manage multiple projects simultaneously, ensuring that all aspects of the clinical monitoring process are performed to the highest standards
• Coordinate and perform all aspects of the clinical monitoring process, including site initiations, monitoring visits, and study close-out activities
• Develop and maintain strong relationships with clients, investigators, and other stakeholders to ensure that projects are delivered to the required standard
• Collaborate with cross-functional teams, including project managers, data managers, and clinical trial coordinators, to ensure that all projects are delivered on time and within budget
• Identify and escalate any issues or concerns that may impact the delivery of projects, and work with the project team to develop and implement solutions
• Develop and maintain a thorough understanding of the clinical trials process, including ICH-GCP, EU, and FDA requirements
• Participate in training and professional development activities to maintain and develop technical and professional skills and knowledge
• Collaborate with the quality assurance team to ensure that all projects are delivered to the required standard
• Develop and maintain a thorough understanding of the company's standard operating procedures (SOPs) and policies
• Participate in internal audits and inspections, as required
• Develop and maintain a thorough understanding of the clinical research associate role and responsibilities, and the skills and knowledge required to perform the role successfully

What We Are Looking For

• University degree in a life-sciences field
• At least 6 months of independent, on-site monitoring experience in a pharmaceutical or clinical research organization
• Demonstrated understanding of ICH-GCP, EU, and FDA requirements
• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
• Excellent communication, collaboration, organizational, and time management skills
• Excellent command of English and local languages
• Ability to work independently and as part of a multinational team
• Strong analytical and problem-solving skills
• Ability to develop and maintain strong relationships with clients, investigators, and other stakeholders
• Strong attention to detail and ability to maintain high-quality records and reports

Nice to Have

• Experience working in a functional service provider (FSP) environment
• Knowledge of the company's standard operating procedures (SOPs) and policies
• Experience working with electronic data capture (EDC) systems and other clinical trial management tools
• Certification in clinical research, such as CCRA or ACRP
• Experience working in a fast-paced, dynamic environment with multiple priorities and deadlines

Benefits and Perks

• Competitive remuneration and annual incentive plan bonus
• Comprehensive healthcare and benefits package
• Opportunity to work with a leading global organization in the life sciences industry
• Professional development and training opportunities, including award-winning training programs
• Collaborative and dynamic work environment with a team of experienced professionals
• Flexible working arrangements, including remote work options
• Access to cutting-edge technology and tools, including electronic data capture (EDC) systems and other clinical trial management tools
• Recognition and reward programs for outstanding performance and contributions

• Make sure to highlight your experience working with Excel and other clinical trial management tools in your application
• Demonstrate your understanding of ICH-GCP, EU, and FDA requirements, and be prepared to provide specific examples of how you have applied these regulations in your previous roles
• Showcase your ability to work independently and as part of a multinational team, and highlight your excellent communication and interpersonal skills
• Be prepared to discuss your experience working in a fast-paced, dynamic environment with multiple priorities and deadlines, and provide examples of how you have managed your time and priorities effectively
• Consider obtaining certification in clinical research, such as CCRA or ACRP, to demonstrate your expertise and commitment to the field
• Research the company's culture and values, and be prepared to discuss how your own values and work style align with those of the organization