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GLP Consultant (f/m)
Eingestellt von Michael Bailey Associates - Munich
Gesuchte Skills: Consultant, Support
Projektbeschreibung
GLP CONSULTANT (M/F)
Location: Bern
Start/duration: ASAP - 31.12.2014 in fulltime
Temp. Contract with negotiable rate per hour
JOB DESCRIPTION
The principal focuses on developing and marketing vaccines and antibodies against a range of infectious diseases in the paediatric, travel and endemic fields.
- Writing of IOQ and PQ protocols and ensuring QA review. Arranging and supervising validation activities. Writing IOQ and PQ reports and ensuring QA review
- You provide support to the entire R&D organization by maintaining and ensuring proper training and adherence to ICH-GCP, SOPs, laws, policies, and local quality systems
- Facilitates implementation of global and local SOPs and policies for the conduct of clinical trials
- you will work together with all functions in the Clinical R&D group (clinical R&D director, LTMs, SMs, CRAs and CTAs) and will have a close collaboration with the unit heads
YOUR PROFILE, QUALIFICATIONS
- Excellent customer service, interpersonal, communication and team collaboration skills
For application please contact or send CV/project list to Frank Arnold
PHARMACEUTICAL RECRUITMENT CONSULTANTMichael Bailey International is acting as an Employment Business in relation to this vacancy.
Location: Bern
Start/duration: ASAP - 31.12.2014 in fulltime
Temp. Contract with negotiable rate per hour
JOB DESCRIPTION
The principal focuses on developing and marketing vaccines and antibodies against a range of infectious diseases in the paediatric, travel and endemic fields.
- Writing of IOQ and PQ protocols and ensuring QA review. Arranging and supervising validation activities. Writing IOQ and PQ reports and ensuring QA review
- You provide support to the entire R&D organization by maintaining and ensuring proper training and adherence to ICH-GCP, SOPs, laws, policies, and local quality systems
- Facilitates implementation of global and local SOPs and policies for the conduct of clinical trials
- you will work together with all functions in the Clinical R&D group (clinical R&D director, LTMs, SMs, CRAs and CTAs) and will have a close collaboration with the unit heads
YOUR PROFILE, QUALIFICATIONS
- Excellent customer service, interpersonal, communication and team collaboration skills
For application please contact or send CV/project list to Frank Arnold
PHARMACEUTICAL RECRUITMENT CONSULTANTMichael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Organisation/Management, Sonstiges