Sr. Clinical Research Associate (Belgium)
WFA Digital Insight
As the demand for clinical research specialists continues to grow, with a notable 25% increase in remote clinical research roles in the past year, Alimentiv is seeking a seasoned Sr. Clinical Research Associate to lead their clinical site monitoring services. This role stands out in the current market due to its focus on digital skills and remote work, offering a unique opportunity for those looking to leverage their expertise in a flexible environment. With the clinical trial industry projected to reach $68.9 billion by 2026, skilled professionals are in high demand. Before applying, candidates should be aware of the importance of strong communication skills, attention to detail, and the ability to build collaborative relationships in this field.
Job Description
About the Role
The Sr. Clinical Research Associate role at Alimentiv is a critical position that involves managing, delivering, and performing full clinical site monitoring services for one or more projects. These projects can be complex, multinational, and may include multiple services. As a lead CRA, you will act as the primary liaison between CRAs and the project team, participating in the development of project plans, protocols, and other monitoring forms and documents.The role requires a strong understanding of clinical research principles, including GCP best practices and regulatory requirements. You will be responsible for the design and oversight of project monitoring services, including training, site and patient recruitment, site data and document management, and monitoring project site budgets.
As a senior member of the team, you will also be expected to act as a subject matter expert, mentoring and coaching junior CRAs, and providing performance feedback to managers. Your expertise will be invaluable in ensuring the successful delivery of clinical trials and the maintenance of high-quality data.
What You Will Do
- Manage and deliver clinical site monitoring services for multiple projects
- Act as the primary liaison between CRAs and the project team
- Participate in the development of project plans, protocols, and other monitoring forms and documents
- Design and oversee project monitoring services, including training and site and patient recruitment
- Manage site data and document management, and monitor project site budgets
- Perform co-monitoring and training visits with CRAs
- Act as the first escalation point for the resolution of site and patient issues
- Represent the company in business development initiatives with a site monitoring focus
- Identify and recruit site investigators and coordinate the movement and delivery of trial materials
- Ensure SOPs are in place to optimize patient recruitment and provide guidance to site teams
- Oversee the overall integrity of the study and promote positive working relationships with sites and staff
What We Are Looking For
- A minimum of a college diploma or degree in a related field
- 4-6 years of experience in clinical research, with a focus on site monitoring
- Strong communication and interpersonal skills
- Ability to work independently and as part of a team
- Strong attention to detail and organizational skills
- Fluency in English, Dutch, and French
- Ability to regularly travel to sites
- Strong understanding of GCP best practices and regulatory requirements
- Experience with clinical trial management systems and other relevant software
Nice to Have
- Experience with electronic data capture systems
- Knowledge of ICH-GCP and FDA regulations
- Certification in clinical research or a related field
- Experience with project management tools and software
- Familiarity with clinical trial protocols and study designs
Benefits and Perks
- Competitive salary and benefits package
- Opportunity to work with a leading clinical research organization
- Flexible and remote work arrangements
- Professional development and training opportunities
- Access to cutting-edge technology and tools
- Collaborative and dynamic work environment
- Recognition and reward for outstanding performance
- Comprehensive health and wellness program
- Generous paid time off and holiday schedule
How to Stand Out
- Tip: Ensure your resume and cover letter are tailored to the specific requirements of the Sr. Clinical Research Associate role, highlighting your experience with clinical trial management systems and GCP best practices.
- Be prepared to provide specific examples of your experience with site monitoring, patient recruitment, and data management during the interview process.
- Develop a strong understanding of the company's culture and values, and be prepared to discuss how your skills and experience align with their mission.
- Consider obtaining certification in clinical research or a related field to increase your competitiveness for the role.
- Research the company's current projects and initiatives, and be prepared to discuss your thoughts on how you can contribute to their success.
- Don't hesitate to ask questions during the interview process, such as what a typical day looks like in the role, or what opportunities there are for professional development and growth.
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