Offer summary

Qualifications:

MD degree with experience in patient care in oncology, 2+ years of experience in clinical development within oncology, Ability to interpret medical safety and efficacy data, Strong communication skills and fluency in English..

Key responsabilities:

Review medical data of ongoing clinical studies in cooperation with the Medical Director

Collaborate with sites, CRO, and Clinical Team to ensure data integrity

Prepare summaries of medical data for discussions in Project Teams

Conduct study-related trainings for internal and external use as required.

Job description

KPS Life is looking for Medical Monitor - sponsor dedicated. This role can be based anywhere in the 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