Clinical Trial Manager

Clinical Trial Manager

Amgen

Paris, France

WHAT YOU WILL DO:

In this vital role you will be the primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up to close out (CSR/Archival) at a country level in accordance with ICH-GCP and other applicable local regulations. You will maintain the quality and scientific integrity of clinical trials at a local/country level and actively collaborate with cross functional internal and external partners to ensure timely delivery, budget execution of clinical trial results within the local country.

Key Activities:

  • Partner with global and local country teams to provide high level country strategy and actively drive study progress and local/country level study delivery;
  • Planning, management and oversight of clinical study execution in accordance with the global program strategy, through leadership with engagement of the cross-functional Local Study Team;
  • Communicate country status (including timelines and deliverables) to key partners including updates to relevant systems for transparency;
  • Provides country level input into the Country Operational Plan and partners with the Development Feasibility Manager through feasibility and with the Global Clinical Managers to ensure local delivery of the study;
  • Support internal audit and inspection activities and contribute to CAPAs, including leading resolution of issues when appropriate e.g., vendor management;
  • Assign and lead all aspects of deliverables of study support staff and continually review country level risk mitigation to ensure study delivers to plan.

WHAT WE EXPECT OF YOU

We are all different, yet we all use our unique contributions to serve patients. The qualified professional we seek is a Trial Manager with these qualifications.

Minimum Requirements:

  • Doctorate degree; OR
  • Master’s degree & 3 years of directly related experience; OR
  • Bachelor’s degree & 5 years of directly related experience; OR
  • Associate’s degree & 10 years of directly related experience; OR
  • High school diploma / GED & 12 years of directly related experience;
  • Advanced knowledge of global clinical trial management;
  • Fluency in local language and business English.

Preferred Requirements:

  • BA/BS/BSc;
  • Minimum 2-3 years’ experience of leading local/regional or global teams;
  • Minimum 2-3 years’ clinical trial project management experience;
  • 7 years’ work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company;
  • Experience in management and oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.);
  • Must be a local/country expert with proven project management experience locally;
  • Must be able to build strong site relationships as well as other local relationships to ensure end to end study delivery is met.

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© EuroJobsites 2022

EuroJobsites is a registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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