KPS Life is looking for Medical Monitor - sponsor dedicated. Anywhere in EU. Contract , hourly rate.
As a Medical Monitor you will be part of the Medical Team and will support the Medical management of clinical trials, ensure the integrity of Medical data and support their interpretation.
Job Responsibilities
- Review Medical data of ongoing clinical studies in cooperation with the Medical Director
- Collaborate with sites, CRO, and Clinical Team to ensure data integrity
- Support development of clinical trial protocol summaries and protocols, reports and publications
- Prepare summaries of Medical data for discussions in Project Teams
- Contribute medical expertise to the execution of clinical trials (including selection of investigators/study sites)
- Review clinical trial reports and summaries
- Support development of study documents throughout the clinical trial course: feasibility questionnaires, pre-study/initiation/monitoring/close-out visit reports, statistical analysis plans, AE reconciliation reports, etc.
- Conduct study-related trainings for internal and external use as required
Qualifications
- MD degree, preferably with experience in patient care in oncology
- 2+ years of experience in clinical development within oncology
- Ability to interpret Medical safety and efficacy data
- Experience with interactions between CROs and pharma companies
- Knowledge of GCP and worldwide regulatory requirements
- Experience in operating in matrix organizations
- Strong communication skills
- English Fluent