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Clinical Project Manager

Switzerland   •  CHF75 - CHF93 per hour  •  Contract/Temporary, Full time

Clinical Project Director
Pay Rate Range: 75.07CHF/hr - 93.84CHF/hr.
Workload: 90% - 100%? 6 Months
Mandatory 3 days per week on site
Remote: to be discussed over interview.  

Job Purpose
As the leader of the cross-functional CLIN site Trial Team (CTT),

  • Leads planning and management of the assigned clinical trial(s) end-to-end to achieve Global Program Team (GPT), Global Clinical Team (GCT), CTT and GDO-TM objectives.
  • Oversees the conduct of clinical trial(s) including budget and resource allocation within assigned trial(s).
  • Drives operational excellence through process improvement and knowledge sharing across trials.
  • Enables an empowered organization that can navigate in a matrix environment and adjust quickly to business needs.
  • Point of escalation for resolution of trial management operational issues within assigned trial(s).

Ideal Background
Education: Bachelor degree or equivalent degree is required, with advanced degree preferred. At least one of the degrees in life science/healthcare is preferred.
Languages: Fluent English (oral and written)

  • ?5 years of operational and managerial experience in planning, executing, reporting global clinical trials in a pharmaceutical company or a contract research organization.
  • Has guided, trained and/or developed direct reports. OR, has mentored and/or served as an onboarding partner in case of no prior people management experience.
  • Proven ability to work independently in a complex matrix environment (including remote or virtual team environment).
  • Strong project management skills and demonstrated ability to meet timelines.
  • Proficient communication, influencing and negotiating skills. Strong interpersonal, problem-solving and conflict resolution skills.
  • Experience in developing effective working relationships with internal and external stakeholders.
  • Organizational awareness, including experience working cross-functionally and in global teams.
  • Proven record of managing resources (budget and headcount).
  • Established knowledge of ICH/Good Clinical Practice, clinical trial design and global drug development process.
  • Good knowledge of relevant therapeutic area(s) preferred.

For further details, please contact Rudo Urayayi on +44(0)1727 817 616 or email a copy of your CV to rurayayi@achieva.co.uk

  • Agency: Achieva Group Limited
  • Reference: RU-143
  • Posted: 12th May 2023
  • Expires: 9th June 2023

Achieva Group Limited

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