Senior Clinical Research Associate (SrCRA)

The genae group is a global, full-service Clinical Research Organization (CRO) which specializes in cardiovascular, endovascular and orthopedic therapies and medical devices and assists in the research, testing and approval processes for products and technologies. genae designs, manages and analyses studies in a wide range of therapeutic areas at all phases of clinical trials. A complete package of trial-related services is offered, from protocol design to medical writing, medical imaging analysis, statistics and data management.

Senior Clinical Research Associate (SrCRA)

Function:

You take responsibility for the administration and monitoring of clinical research projects according to our Standard Operating Procedures, the ICH-GCP Guidelines and ISO 14155.
You analyze and evaluate clinical data, ensure compliance with protocol and overall clinical objectives; identify, select, initiate and close-out appropriate investigational sites for clinical studies.
You monitor the sites in order to ensure that studies are carried out according to the applicable regulations and guidelines.
You act as mentor of junior staff members

Profile:

By preference, you have a (para-) medical or scientific degree and at least three (3) years of clinical research experience (monitoring).
You have excellent planning and organizational skills with good negotiation, time-management and people skills.
You are fluent in English and by preference in other languages as well.

Offer:

Offer:

We offer tough but fascinating jobs that requires attention to detail, regular international travel and a competitive compensation & benefits package in a permanent employment position.
genae is committed to diversity and is an equal opportunity employer.

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Senior Clinical Research Associate (SrCRA)