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Associate Manager, Clinical Operations 0,6 FTE, Czech Republic - FSP

Employer
Labcorp
Location
Czech Republic
Salary
Competitive
Start date
20 Sep 2021
Closing date
27 Sep 2021

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Discipline
Clinical Research, Clinical Operations
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details


As an Associate Manager, Clinical Operations, you would be responsible for the supervision of of assigned direct reports within Clinical Operations, FSP and/or Global Site Services as well as the Sponsor interaction.

Key Responsiblities:
  • Responsible for detailed performance review and management of assigned direct reports including: Annual Performance Management and Development (PMD), Individual Development Plan (IDP), Line of Sight Goals and "Shoves & Tugs"
  • Responsible for appropriate management and resolution of performance issues
  • Develop and measure performance indicators for assigned staff
  • Identify individual training needs and assist with the coordination and conduct of training and development efforts, regionally
  • Coordinate, conduct, report and follow-up on Quality Control Visits (CQC)
  • Effectively communicate management strategies, policies and procedures in conjunction with leadership teams
  • Develop and maintain effective relationships with management team to manage assigned staff in a matrix environment
  • Maintain good working relationships with internal and external clients to ensure opportunity for acquiring additional new business
Education/Qualifications:
  • University/college degree - life sciences preferred or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
  • In lieu of this required educational background the following relevant work history may be considered:
  • Proven supervisory experience in a health care or clinical research setting and
  • Relevant clinical research experience in a pharmaceutical company/CRO
Experience:
  • Relevant clinical research experience in a pharmaceutical company or CRO
  • Individual is proficient with on site monitoring activities (including pre-study, initiation, routine monitoring and closeout visits)
  • Proven relevant clinical research experience in a pharmaceutical company/CRO
  • Thorough knowledge of drug development process
  • Thorough knowledge of relevant SOPs, ICH, and GCP guidelines
  • Relevant supervisory experience
  • Minimum of 3 years as a Line Manager or Project Manager required
  • Demonstrated ability to lead by example and to encourage team members to seek solutions
  • Proven interpersonal skills
  • Demonstrated ability to successfully participate as a member of a project team
  • Demonstrated ability to successfully manage multiple competing priorities
  • Advanced planning and organizational skills
  • Advanced oral, written and presentation skills

Company

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom

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