Clinical Research Associate (candidate pool)
- Undefined
- Pharmaceutical
Novellas Healthcare is seeking a proactive CRA to coordinate, oversee, and monitor clinical trials at investigator sites. The CRA will be involved in all aspects of the clinical trial process, from recruiting study participants to collecting patient data and performing quality assurance audits to ensure study protocols are followed.
Vacancy information
- Establish trial sites, train site staff, and manage investigational products (IP) and trial materials
- Manage multiple aspects of subjects' welfare, review patient enrollment, and conduct regular visits to clinical sites
- Prepare study documents, liaise with interested parties, and ensure patient safety and data integrity
- Generate and oversee documentation and records to ensure compliance with protocol, SOPs, local regulations, and ICH and GCP guidelines
- Organize investigator payments
Requirements information
- Master degree in life sciences or equivalent through experience
- Knowledge of pharmaceutical industry, terminology, and practices
- Knowledge of ICH/GCP, Belgium Clinical Trial regulations and their practical implementation
- Strong verbal and written communication skills
- Proficient computer skills, including MS office, eTMF, and CTMS systems
- Ability to manage and prioritize workload effectively
- Fluent knowledge of Dutch, English and French
- Excellent planning and organization abilities
- Ability to work with minimal supervision/autonomous
- Pro-active problem-solving skills
- Good negotiation skills
The ideal candidate for this role will be detail-oriented, have the ability to multitask, and be able to collaborate with various role players. He/her should be able to recognize logistical problems and initiate appropriate solutions.
If you are a motivated, skilled CRA looking for an exciting opportunity, we encourage you to apply!
