Clinical Trial Leader

Basel  ‐ Onsite
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Keywords

Description

Is there a better way to start the summer than with a new, exciting and vibrant job within the Pharma industry? Read about the position below and make sure you get the best start for this summer.

A leading pharmaceutical company is currently seeking a Clinical Trial Leader (CTL) in Basel for 6 months. This is a global pharmaceutical company with presence in varies countries around the world. They are well-known for their ability in pioneering science. They operate an open-minded environment, particularly within clinical study teams. This is a role with responsibility, where you will be empowered with the relevant decision-making authority, but will equally be accountable for your actions and responsibilities. This is an international, English-speaking environment.

This position requires the following skills:
  • An advanced degree in life science/healthcare or equivalent, with at least 4years experience in clinical trials from a technical and operational side
  • Ability to work within matrix organizations, individually and in a team
  • Strong negotiation skills
  • Excellent knowledge in Good Clinical Practice (GCP)
  • Hands-on experience in data cleaning and analysis
  • Basic understanding and experience of Oncology and Haematology is a clear advantage


This position entitles these main duties:
  • Contribute to the development of clinical sections of regulatory documents like Investigators' Brochures, briefing books, safety updates, IND/NDA submission documents, responses to Health Authorities questions.
  • Lead and matrix manage the global multidisciplinary CTT to ensure all trial deliverables are met according to timelines, budget, and resource requirements; speaks up against unrealistic timelines. Energizes CTT to adhere to global performance and quality standards: chair CTT meetings, report study progress and issues with their resolution plan. Engages the input of line functions at the appropriate time. Leads trial level interactions with Global Monitoring Operations (GMO) and other relevant functions including Integrated Medical Safety and Drug Supply Management.
  • In collaboration with the CPL lead the clinical trial data ongoing medical/scientific review, final analysis and interpretation including the development of clinical trial reports, publications and internal/external presentations.


If you fulfill the minimum criteria and are interested in this position or similar ones, contact me today, for immediate consideration.

Sebastian Spaniol
Email: s.spaniol"@"realstaffing.com
Tel.:
Start date
07/2014
Duration
6 Months
From
Real Staffing
Published at
12.06.2014
Project ID:
724691
Contract type
Freelance
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