Do you have experience in Clinical Contracts and Budgets management with sites and want to extend and share your experience in a growing, dynamic, global company with a very nice familial team spirit? Don't hesitate and apply now!
Job Description
As a Study Start-Up Specialist, you will be providing direct operational support to project teams and ensure that clinical projects start smoothly and on time.
Responsibilities
- Develop and negotiate site contracts and budgets
- Collect, review, and submit documents for ethics and regulatory review and approval
- Prepare packages of site documents for drug release to clinical sites
- Communicate with project teams, investigative sites, review bodies, vendors, and clients regarding start up matters till the moment of site activation
- Monitor start up metrics and timelines
- Support site identification and selection process
Requirements
- College/University degree or an equivalent combination of education, training and experience
- Ay least 2 years full-scope study start up experience
- C2 level in Dutch, full working proficiency in English and French
- Ability to negotiate and build relationships at all levels
- Ability to plan, multitask and work in a dynamic team environment
- Excellent communication and collaboration skills
Benefits
- Full-time position.
- Hybrid working policy (3 days/week home-based)
- A balanced salary package based on your capabilities and experience, including extra-legal benefits.
