CLINICAL PROJECT MANAGER H/F

Job description

As a Contract Research Organisation (CRO) and major player in clinical research, Keyrus Biopharma has been has been sharing its clinical research experience with pharmaceutical industries, food industries and biotech companies in the development of drugs and other products such as nutritional products, medical devices, cosmetics and contrast products. KBP’s employees are specialised in all areas of clinical trial services: regulatory submissions, feasibility studies, study set-up and monitoring, data management, biostatistics and medical writing, and work in a variety of development phases e.g. preclinical, clinical phases I to IV, epidemiology and surveys, all the while respecting SOPs and ICH GCP.
Today, Keyrus Biopharma provides expertise and consultancy in all clinical research areas on the basis of this experience and has adapted to the requirements of new environments / areas such as nutrition, biotechnology, cosmetology and medical devices
We are looking for a Clinical Project Manager:
Main tasks:
- Full management of study: planning, timelines, budget, deliverables and procedures
- Management of studies according to GCP-ICH
- Coordination of the various study personnel e.g. providers, central laboratories, affiliates
- Participation in writing study documents e.g. protocol, CRF, informed consent form
- Liaison between the various departments i.e. regulatory affairs, biometry, medical officer, finance
- Reporting to the sponsor
- Training and supervision of clinical research associates
Required skills and qualities:
- Excellent level of English and French (spoken and written)
- Good command of office software (Excel, Word, PowerPoint)
- Moderator of meetings, training and telephone conferences (English and French)
- Management skills
- Attention to detail
- Organized, pro-active, autonomous
- Good interpersonal skills
- Good oral and written communication
Required level of education and experience:
- Scientific University degree or equivalent with subsequent training in clinical trials
- At least 2 years experience in clinical project management in a CRO or pharmaceutical company .
- Experience in international projects.
- Good command of a third language e.g. German, Spanish is a plus
Our offer
- Company car, petrol card, meal vouchers, group insurance, hospitalization…. Each employee will be welcomed with a varied integration program. We invest considerable time and resources in training our staff (technical and non-technical courses). You will join a dynamic and international environment with enthusiastic and professional colleagues.