Description
Senior Clinical Operations Manager (m/f)
Reference: -en
Start: asap
Duration: 12 MM++
Main tasks:
- Directs the planning, set-up and conduct of trials (phase 1 to phase 3)
- Prepares trial budgets, forecasts, timelines, and project plans
- Negotiates contracts and budgets for assigned clinical trials
- Support close CRO surveillance and management of other third party vendors
- Reviews clinical study protocols and provides input
- Prepares clinical trial supplies projections and ensures the availability of a supply chain during the whole conduct of the trial
- Supervises training programs to assure consistency and compliance in conduct and monitoring of clinical trials
- Prepares status reports for assigned clinical trials
- Participates in internal/external audits
Main qualifications
- Profound and progressively increasing clinical development experience within the pharmaceutical industry
- Experience in clinical operations/clinical trial management especially in outsourced global phase 3 trials
- Monitoring experience
- Advanced academic degree (M.S., PhD or MD) is preferred; at the minimum an academic degree in Life Sciences, Pharmacy or Medicine is required
- Communication skills (fluency in English mandatory)
Main advantages:
- Pleasant working atmosphere
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Tina Maric
Referencenumber:
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