If you are looking for a challenging Study coordinator position within an oncologic Phase 1 unit then this is the place to be.
Job Description
You will be responsible for the coordination of clinical trials from A to Z in a very dynamic team.
Responsibilities
- Coordination of Phase I oncology clinical trials
- Data entry and data management
- Contact with patients
- Data collection during patient visits
- Planning of Trial visits
- Safety reporting (AE, SAE's)
- Administrative follow up (e.g. Investigator Site File)
- IMP handling
Requirements
- A degree in life sciences
- 1 to 5 years of experience in coordinating clinical trials
- Good knowledge of oncology
- Good knowledge of ICH-GCP
- Experience in early phases trials is a plus
- Very strong time management skills
- Languages: French, English
- Strong communication skills
- Autodidact
- Proactivity
- Team player
- Flexibility
- Strong organizational skills
- Stress resistant
Benefits
- Full time or part time position
- A balanced salary package based on your capabilities and experience
Existing right to work in Europe required ( please read job spec in full before applying ).
Vacancy number: 17207
