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Local Trial Manager

extra holidays - extra parental leave
Remote: 
Full Remote
Contract: 
Experience: 
Expert & Leadership (>10 years)
Work from: 

Offer summary

Qualifications:

Doctorate degree or Master’s degree and 3 years of experience, Bachelor’s degree and 5 years of experience, Associate’s degree and 10 years of experience, High school diploma with 12 years of experience.

Key responsabilities:

  • Lead and coordinate clinical trials from start-up to close out
  • Manage country level input into operational plans and timelines
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AMGEN Biotech: Biology + Technology Large http://www.amgen.com
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Job description

Career Category
Clinical
Job Description

Local Trial Manager

Full time position

Manager: Global Clinical Trial Manager

Employment contract for 1 year, possibly prolonged to indefinite period of time

Home location of candidates anywhere in the Czech Republic

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 implementation 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 implementation in accordance with the global program strategy, through leadership with engagement of the cross-functional Local Study Team
  • Communicate country status (including timelines and results) 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 deliver all study support staff and continually review country level risk mitigation to ensure study delivers to plan

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

  • 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 identifiable project management experience locally
  • Build strong site relationships as well as other local relationships to ensure end to end study delivery is met.

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Required profile

Experience

Level of experience: Expert & Leadership (>10 years)
Industry :
Biotech: Biology + Technology
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Leadership
  • Relationship Management
  • Time Management
  • Teamwork
  • Communication
  • Problem Solving

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