Tired of monitoring? Want to manage instead? CRA Coordinator Brussels Job in Belgium
Tired of monitoring? Want to manage instead? CRA Coordinator Brussels
CRA Coordinator in BRUSSELS 45K - 60K
My client is a pharmaceutical company with the mission to improve the lives of patients by creating medicines that cure dangerous and possibly life threatening diseases. They focus the efforts of their employees on discovering new medicines to help prevent or cure those diseases. They are looking for new staff to further help them capitalizing on the business development.
To ensure their continued growth my client is looking for a experienced (Senior) Clinical Research Associate to act as CRA Coordinator.
This person will play a pivotal role in the clinical studies conducted across various European locations and this person will also be in close contact with the various counterparts in the US. Therefore, international travel is an integral part of this job (max 20%).
Responsibilities:
- Provide direction and guidance as mentor for clinical research associates and conducts co-monitoring/training visits.
- Develops and implements innovative approaches for site selection and pre-study activities to identify and evaluate potential investigators
- Manage investigator grant development and payment processes
- Manage vendor invoice review
- Review monitoring trip reports and coordinates resolution of global and/or site specific issues.
- Review and assess the status of global and site specific clinical data on a ongoing basis
- Manage clinical audit review/resolution processes
- Participate in study feasibility and protocol/case report form development
- Participate in quality improvement initiatives to increase operational efficiency
Requirements:
- Bachelors Degree in nursing, life sciences or a similar combination of education and experience
- 4-5 years of clinical monitoring experience, minimum 3 years field monitoring
- CRA team management experience
- Thorough knowledge of clinical research principles, ICH-GCP and FDA regulatory requirements
- Good verbal and written communication skills.
- Highly organized
- Detail oriented
- Ability to multi-task and work in a flexible and dynamic organization
- Ability to anticipate/identify potential problems and implement correction actions
- Willingness to travel occasionally (max 20%)
- Must be proficient in Microsoft Word and Excel
Does the above appeal to you and would you like to find out more about the rewards, challenges and opportunities this pharmaceutical company offers?
Then contact David Marimuthu Clinical Operations Consultant at Real Pharma Amsterdam on +31 (0)20 522 1577 or submit your cv directly via the button.
(Real Staffing Group acts as an Employment Agency and an Employment Business)