Careers

To care about, and to take care of clinical research.

genae considers people its most valuable asset. Each member of our organization makes a valuable contribution to our success and the success of our clients. We offer interesting jobs in a prestigious, international environment and a competitive compensation & benefits package in a permanent employment position. We are committed to diversity in the workplace and we are an equal opportunity employer.

genae is always looking to meet with talented individuals to fulfill positions in clinical trial management, data management, sales & marketing, quality, customer support, business development.

To apply, send a cover letter and resume to:

genae associates nv
Human Resources
Paleisstraat 24
2018 Antwerp, Belgium
E-mail: hr[at]genae.com

Current job opportunities (updated: March 1, 2010):

Two Clinical Project Managers (CPM)

Function: You take responsibility for overseeing and coordinating the start-up, progress and closure of clinical research projects. You pro-actively identify study related matters and set-up strategies to handle these effectively. You report to all relevant parties on a regular base and on request while managing the clinical research project budget in close cooperation with the Sponsor. In order to align your project team with the project objectives, time-lines and budget, you direct, guide and support them. You are prepared to travel in the European Union and abroad on a regular basis.

Profile: By preference, you have a (para-) medical or scientific degree (biology / pharmacy) and at least four years of clinical research experience (monitoring experience). You have excellent planning and organizational skills with good negotiation, time-management and people skills. You are at least fluent in English and by preference in more European languages.

Location: CRO office in Antwerp. Occasional international travel required

Three Clinical Research Associates (CRA)

Function: You take responsibility for the administration and monitoring of clinical research projects according to our Standard Operating Procedures, 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.

Profile: By preference, you have a (para-) medical or scientific degree (biology / pharmacy) and at least one year of clinical research experience (including monitoring) or a minimum of two years experience in pharmaceutical data management or as a study coordinator. You are a detail oriented professional with good negotiation, time-management and people skills. You are at least fluent in English and by preference in more European languages.

Location: CRO office in Antwerp. Regular international travel required