Clinical Research Physician - Brussels, België - EORTC

EORTC

Geverifieerd bedrijf

Brussels, België

3 weken geleden

Geplaatst door:

Sophie Dubois

beBee Recruiter

Beschrijving

The Clinical Research Physician provides medical expertise and support for the development, implementation, conduct and reporting of EORTC clinical trials.

He/she also supports the EORTC Research Groups in the elaboration of their scientific strategies to improve standards of care.

Main responsibilities / Major Activities
Strategy

Clinical Research Physician (CRP) supports the EORTC Research Groups in the elaboration of their scientific strategies to improve standards of care.

The CRP contributes to building strong interactions between the stakeholders (academic groups, industry).

Through his/her activities with different EORTC Research Groups, the CRP facilitates cooperation and the cross-fertilisation of ideas among the groups.

Clinical trials

The CRP provides medical expertise and support for the development, implementation, conduct and reporting of EORTC clinical trials.

He/she works together with Data Managers, Projects Managers, Clinical Scientists and Statisticians as part of the EORTC Headquarters teams supporting the studies carried out by the EORTC Research Groups.

He/she also contributes to the Board form, outline and writing of protocols and the design of case report forms.

Throughout the study, he/she makes an active contribution to the trial management by leading the medical monitoring process:

support sites for enrolment, monitoring of recruitment and study data, medical education, maintenance of protocol, preparation of study reports and safety reporting to Regulatory Bodies, preparation, and meetings with DSMB or IDMC, support audits and attendance to meetings.

Education

The CRP conducts training for the non-medical staff. He/she contributes also to courses and workshops organised by the EORTC and other organisations.

Profile
A Medical Doctor degree
Minimum 5 years of professional experience, preferably in Oncology
Experience as a clinical trialist or medical monitoring
Basic understanding of medical statistics
Experience in the pharmaceutical industry is an asset
Must be fluent in English (oral and written), other languages are an asset
Team player and dynamic
Good level of computer literacy
Availability to travel

Benefits:

Permanent contract
Competitive salary package
Hybrid working environment
30 days holidays (full time)
Free parking
Meal vouchers
Hospitalisation insurance
Pension plan
Reimbursement of public transport
Homeworking allowance