Clinical Trial Leader (m/f/d)

Location
Basel
Salary
Competitive
Posted
15 Oct 2020
Closes
14 Nov 2020
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Luye Pharma Switzerland AG, located in the center of Basel is the European Headquarter of the Luye Pharma Group. Our multicultural and international team is laying the foundations for future products and continued innovation in complex dosage forms – especially transdermal patches. As part of the Chinese Luye Pharma, we are also developing the European business of this dynamically growing, sophisticated pharmaceutical company, which today employs over 4,000 people worldwide.

 

Clinical Trial Leader (m/f/d)

 

Key responsibilities

  • Definition and update of clinical development plans
  • Prepare and / or review study-related or essential study start-up documents as they relate to the assigned clinical trials (e.g. Clinical Protocols, Informed Consent Forms, Investigator Brochures, Pharmacy Manual, Monitoring Plan, Laboratory Manual, Patient Diary, Clinical Site Procedures Manual, Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans and charters)
  • Partner with internal and external experts and consultants
  • Review, analyze and interpret the results of clinical programs in collaboration with relevant experts
  • Provide medical / clinical input into and review of regulatory documents, during development, submission and defense
  • Ensure that the Study Management team meets or exceeds the timelines and deliverables assigned to the study team
  • Develop and manage group of studies for an entire business unit or large development team

 

Requirements

  • Bachelor's degree required, preferably in the life sciences (Chemistry, Biology, Pharmacy), clinical or other relevant technical areas. Advanced degree desirable (e.g. MS, PhD, MPH, PharmD, MD)
  • Minimum of 4 years study management experience. Minimum 5 years of clinical study experience, especially in pharmacokinetic / bioequivalence trials, including the proven ability to oversee clinical teams in the conduct and report of multicenter, global complex studies
  • Profound knowledge of GCP regulations, clinical trial concepts and practices, including international clinical research guidelines
  • Advanced understanding of clinical medicine, clinical pharmacology and associated disciplines (e.g., biostatistics)
  • Ideally experience in clinical development of transdermal patches

 

What we offer our employees

  • Luye life balance: flexible work-time models and the possibility of working partially from home
  • State-of-the-art facilities and equipment
  • Competitive and fair remuneration
  • Attractive benefits
  • Centrally located workplace in the old town of Basel

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