Clinical Trial Manager

Employer
Medella Life
Location
Germany
Salary
€75,000
Closing date
16 Oct 2020

View more

Discipline
Clinical Research, Clinical Trials Manager / Administrator
Hours
Full Time
Contract Type
Permanent
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Responsibilities

  • Support the clinical protocol development process in collaboration with the Head of Clinical Operations and the Medical Monitor: Contribute in the development of clinical protocols, amendments and related documents; drive and/or contribute to the development of trial-related documents and processes
  • Lead the development of study tools, guidelines, and training materials to support effective and accurate execution of clinical trial activities
  • Develop relationship with Investigators and Site Staff as primary contact for clinical conduct of the trial
  • Under the guidance of the Head of Clinical Operations, manage study start-up activities including regulatory documents, budget, and clinical trial agreements
  • Participate in the ongoing review and cleaning of the clinical trial data
  • Chair study team meetings, collecting input from all functional lines
  • Participate in site identification; attending PSVs and SIVs as necessary
  • Assist in the management of 3rd party vendors; including CRO, central lab and imaging vendors
  • Manage tracking, logistics and quality operations for biological samples supporting clinical trials from collection to analysis ensuring that sample inventories are accurate, complete, and up-to-date through effective interactions with internal teams, sites, central reference labs, specialty lab partners, external collaborators (e.g. Academia) and third-party vendors
  • Ongoing management of accurate enrolment log/trial allocations forms
  • Ensure compliance with patient consent for collection and intended use, destruction, storage and/or future, post-study use of biological samples
  • Communicate with management to ensure transparency throughout the course of the trial(s) regarding study metrics and overall status

What you have to offer.

  • BA/BS degree required
  • Minimum of 4 years of experience in clinical drug development or clinical trial execution with exposure to biomarkers or immunogenicity sample activities including sample collection procedures and logistics considerations
  • Advanced skills in Microsoft Office programs as well as good working knowledge of electronic data systems
  • Detailed and precise record keeping skills are essential as well as the ability to track and resolve issues
  • Excellent teamwork, communication (verbal and written), organizational, and interpersonal skills
  • Self-motivated, proactive, and able to prioritize and manage multiple projects simultaneously

Company Profile

As specialist recruiters in life sciences, our mission is to create a positive impact in the world. We place visionary people in thriving cultures where they can create a brighter future. Our impact and what that means to society is why we go the extra mile. We even baked it into our name, Medella, which means to heal. Pairing brilliant scientists with brilliant companies we find wildly exciting, and it drives everything we do.  

​No matter how hard, at Medella Life we live by our values. We may be new, but we are here to earn our stripes. Our founding team has more than twenty-five years experience in the field. Our mission is to be your first call when looking for A-list talent. What matters to us is being the best, not being the biggest. That's why we value quality over quantity. It is our belief that science can save the world. Which is why a Medella Life is a good life.

Contact Us
  • 10 York Road
  • London
  • SE1 7ND
  • United Kingdom
  • +44 20 4511 0354
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