Clinical Scientist

il y a 4 jours


Brussels, Belgique EORTC Temps plein

The Clinical Scientist works under the hierarchical supervision of the Head of the Medical Department. As a member of the Medical Department, and in close collaboration with Clinical Research Physicians, he/she provides scientific support to Disease Oriented Group activities and throughout the entire course of clinical studies conducted at EORTC.

**Main responsibilities / Major Activities**:
**New project development**
- Provide strategic and operational support to the EORTC disease-oriented groups in their project development
- Provide scientific input including:

- develop study concepts including scientific rationale, in close collaboration with the statistician
- assess preliminary feasibility
- define the scope of the project, in close collaboration with the project manager
- Coordinate the involvement of external committees, groups of experts, and headquarters (HQ) based teams to guarantee superior quality of projects
- Initiate and develop relationships with industrial or academic partners both for collaboration on individual studies and to support longer-term partnership opportunities

**Strategic endorsement of new projects**
- Coordinate the strategic review of new study concepts
- Collaborate with the Principal Investigator, Disease Oriented or Transversal Group experts as well as HQ based-scientific teams in the preparation of the project submission
- Support the principal investigator in identifying possible funding for the project

**Synopsis and protocol development**
- Provide scientific and medical input for the development of the synopsis and protocol documents
- Work closely with HQ-based stakeholders to ensure the optimal implementation of endorsed projects

**Study conduct**
- Perform medical monitoring activities for clinical studies, with the support of a Research Physician and in close and dynamic collaboration with a multidisciplinary team (project, operations, regulatory, pharmacovigilance and data management, monitoring)

**Interaction with EORTC network**
- Support Disease-Oriented-Groups in their project portfolio management and guide them through EORTC internal processes
- Establish and maintain high-quality relationships with EORTC group members and experts, by attending Group Meetings and Scientific Events

**Department activities**
- Drive and be accountable for processes related to medical management of studies
- Participate in the discussion, review, and updates on processes related to study conduct

**Profile**:

- Biomedical Ph.D. and a minimum 5-year professional experience in clinical research or Nursing degree with at least 5 years of experience in Oncology and clinical research
- Experience in the pharmaceutical industry is an asset
- Able to write and check content and quality of scientific documents
- Process-oriented
- Must be fluent in English (oral and written), other languages are an asset
- Must be able to work within a team and take responsibilities and initiatives
- Good communicator with a broad range of stakeholders (academia, pharmaceutical industry, biotechnologies)
- Good level of computer literacy

**Benefits**:

- 30 days holidays- Competitive Salary Package- DKV Hospitalization insurance- Free parking- Hybrid working environment- Full reimbursement public transport- Meal vouchers- Pension plan- Permanent contract- Homeworking allowance


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