Clinical Project Manager, Late phases - Homebased possible (60%)

Location
Canton of Geneva (CH)
Salary
Competitive
Posted
08 Apr 2021
Closes
08 May 2021
Ref
(897234-SLV)
Hours
Full Time
Contract Type
Contract
Experience Level
Experienced (non-manager)

Our client is a well-established non-profit organization focusing on developing innovative medicines for improving people’s health and quality of life through a public-private partnership model. With a rich pipeline, the company and its partners continuously invest in innovation and growth. For our client we are currently searching for a Clinical Project Manager for a 2 years contract in the Geneva area. Our client is open to remote/home-based candidates (living within Switzerland).

Main responsibilities:

  • Support Global Study Team Lead in ensuring compliance with quality and regulatory framework, as well as relevant  SOPs;
  • Support Global Study Team Lead in tracking timelines and milestones;
  • Liaise with and oversee the work of country Study Managers / Project Managers;
  • Participate in the review of country-specific documents for consistency with MASTER documents and template tools;
  • Develop and maintain overall budget based on individual studies’ budgets, risk log based on individual studies risk management plans;
  • Review monthly study progress reports/monthly dashboard from each country and flags delays/bottleneck/new risks to Global Study Team Lead;
  • Collate all national regulations that are pertinent from Country Teams;
  • Work with country teams to map out process and list requirements for country IRB approval;
  • Support Global Study Team in defining data management SoW and budget;
  • Establish and maintain study documents tracker;
  • Work with coordinator to ensure all study documents are filed by respective teams;
  • Work with coordinator to prepare submission packages and coordinates responses following review in close collaboration with Global Study Team;
  • Support country teams in developing recruitment projections and monitoring recruitment rates throughout the study;
  • Act as a liaison between Data Management vendor and Global Study Team. (is a strong advantage).

Requirements:

  • Relevant working/residency permit or Swiss/EU-Citizenship required;
  • Minimum Bachelor's Degree in Life Sciences;
  • Strong project management and coordination skills;
  • Thorough understanding of trial management processes;
  • Knowledge of late phase requirements and observational studies.

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