Location: Home based - Germany, EU
In this opportunity you will be working as a project lead in complex global studies in a wide variety of therapeutic areas.
Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
Serve as primary Sponsor contact for operational project-specific issues and study deliverables
Maintain in depth knowledge of protocol, therapeutic area, and indication
Provide cross-functional oversight of internal project team members and deliverables
Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report
Develop operational project plans
Manage risk assessment and execution
Responsible for management of study vendor
Bachelor’s degree in life sciences
Minimum of 5 years’ experience in managing clinical trials
Previous experience working a CRO environment
Experience working across several therapeutic areas and multiple countries
Experience with bid defences and contact with clients
Strong leadership skills
This opportunity is a full time, home based and comes with a competitive salary and bonus program!
If you are interested in applying or hearing more about this opportunity, then please do get in touch for a confidential discussion on your experience and plans for progression. Call Grace on + 441293 584300.
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