CMS Operations Manager

Basel  ‐ Vor Ort
Dieses Projekt ist archiviert und leider nicht (mehr) aktiv.
Sie finden vakante Projekte hier in unserer Projektbörse.

Schlagworte

Beschreibung

Clinical Management Operations Manager (m/f)
Reference:
9726KS
Area:
Medical
Location:
Basel
Start:
asap
Duration:
6 months
Introduction:
For our client we are searching for a Clinical Management Operations Manager to start as soon as possible.
Role:
Manage all operational aspects of clinical trials / projects accountably including trial allocation according to patient accessibility. Perform trial feasibility assessment together with the organization and ensure optimum utilization of resources in cooperation with the Regional Heads and setting of realistic timelines together with the Clinical Team and organize input to the protocol design. Track performance and quality aspect.
Responsible for supporting the Clinical Project Manager (CPM) in the conduct of clinical trial(s) activities as assigned. Ensure all operational trial deliverables are met according to timelines, budget, operational procedures and quality standards.
Deputize for CPM in interaction with Sponsor(s as needed).
Anforderungen:
Education (minimum/desirable): Life Science/Nursing degree or equivalent.
Experience/Professional requirement:
At least 5 years experience in clinical development/project management, including involvement in cross-functional, multicultural and international clinical trial teams; demonstrated capabilities in leading specific trial related activities like planning, executing, reporting and publishing activities. Excellent communication, organization and tracking skills. Strong operational skills and demonstrated ability to meet timelines. Proven ability to work both independently or in a team setting, including a matrix environment.
Knowledge of Good Clinical Practice; thorough knowledge of clinical trial design; understanding of the overall drug development process. Good leadership, negotiation and project management skills. Robust knowledge of the regulatory and local requirements within regions and countries. Demonstrated ability of establish effective working partnerships. Medical / Scientific knowledge of the assigned therapy area and associated trial designs. Demonstrated presentation and diplomacy skills.
Languages: Fluent English (oral and written). German would be advantageous
Start
04/2013
Dauer
6 months
Von
ITech Consult AG
Eingestellt
19.04.2013
Projekt-ID:
524011
Vertragsart
Freiberuflich
Um sich auf dieses Projekt zu bewerben müssen Sie sich einloggen.
Registrieren