Study Level Clinical R&D Lead

We have an exclusive 6 month contract role available to work onsite with a renowned Pharmaceutical company in Brussels, Belgium. This is an opportunity to participate in the clinical development activities for a program or product/franchise within company in order to ensure the high quality and on-time delivery of clinical data that will allow world-wide registration in compliance with the clinical development plan, good clinical practices (GCP), and company's standard operating procedures (SOP). Study Level Clinical R good stage presence for public speaking
- Strong technical, statistical and computer skills and the ability to interpret complex clinical data and experimental results.
- Excellent French & English speaking & writing skills

Experience:

- Sound scientific background required to critically evaluate all scientific aspects of

vaccinology/immunology

- Proven expertise in clinical research (at least 2 years) with international Good Clinical
- Practice Guidelines, basic knowledge of human experimentation laws and regulations.

We welcome applications of consultants' who match most of the above requirements and are available on a short notice. There is a competitive Hourly rate available for the contract, alternative market rates are also welcome. Please note there is a job description available on request and there is a likelihood of the contract extending into 2016.

Kind regards,

Neha Sharma

MBA Michael Bailey Associates

Job Code: 105865

Keywords: Clinical development, SOP, clinical data management, PHARMACEUTICAL, QC, Quality control, Biopharmaceutical, Biotech, CIOM, Quality check, data entry, ICH, GCP, CTA, clinical trials, clinical project management immunology, vaccinology, clinical research, French, English

Michael Bailey International is acting as an Employment Agency in relation to this vacancy. Michael Bailey International is acting as an Employment Business in relation to this vacancy.