Experience

Between 3 and 6 years of CRA experience

Education

Pharmaceutical Sciences or scientific background

Languages

Dutch, English, French

Sector

Pharmaceutical industry

Region

Brussels

Job type

Permanent contract full time

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Clinical Development Consultant

Job description

The CDC os a primary interface between Lilly and investigators in aspects of Clinical Research. He/she is partners with the TPO on interactions with investigators. The CDC is responsible for new sites-prospecting, for site identification and site selection during the FPA process. The CDC is accountable for delivering all regional, local and corporate portfolio commitments/milestones for sites and trials within responsability.

- primary interface with investigators

- collaborate with partners, Quality and other study team members to resolve/escalate site specific issues

- manage site enrollment performance

- manage and develop strategic relationship with current and future investigators

- potential new sites-prospecting 

Skills & Personality

- Deep scientific understanding - Therapeutic area knowledge (Master in Science or equivalent)

- Strong, technical, operational Clinical Operations expertise

- Fluent in English

- Work autonomously

- Team player

- Strong interpersonal skills, emotional intelligence

- Act proactively within responsability

- Good communication skills

- Conflict resolution

- Willingness to travel

Salary Package

Competitive salary