clinical operations lead / bopm in Basel

posted
contact
Audrey Bisch, Basel Professionals Health Care & Life Sciences
job type
contract
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job details

posted
location
basel, basel-stadt
sector
life sciences
job type
contract
reference number
17457
contact
audrey bisch, basel professionals health care & life sciences
phone
058 201 55 50

job description

Do you want to work in a big pharmaceutical company? Do you have at least 1 years experience in pharma industry in clinical operations? You should then read the following lines!

Our client, based in Basel, is looking for a passionate Clinical Operations Lead / BOPM  for a one year contract with possibility of extension.

 

Your  Responsibilities:

  • Provide BIOMARKER OPERATIONAL EXCELLENCE by planning, coordinating, and overseeing all operational activities for the lifecycle of biomarker and companion diagnostic samples and data, for clinical studies.
  • Collaborate with cross-functional STUDY and BIOMARKER TEAMS to execute biomarker operational strategies.
  • Lead identification, selection and oversight of BIOMARKER VENDORS, ensuring quality delivery and performance.
  • Develop and oversee biomarker analysis TIMELINES, BUDGET, RISK, COMPLIANCE and QUALITY, ensuring study adherence to ICH/GCP and SOPs.
  • LEAD AND INFLUENCE by establishing yourself as a leader within the team, inspiring others to perform at their best and learn from biomarker operations best practices. You will be shaping our capabilities and evolving your role over time.
  • DESIRABLE EXPERIENCES: Background in life sciences. Laboratory experience in a clinical / biological / diagnostic setting. Project management. Experience in a pharmaceutical/biotechnology R&D environment.
 

Your Profile:

  • Min Bachelor/Master in Life Sciences (biology and/or chemistry) (PhD & Post Docs are considered) 
  • Minimum 3 years of experience in a clinical research setting, including at least 1 year working in pharma clinical operations
  • Strong experience with vendor and project management
  • Possess strong knowledge of drug development process and respective regulations, including ICH and GCP guidelines 
  • Have a clinical or laboratory experience with evidence of involvement in the processing and/or analysis of biological sample
  • Experience working in a global and matrix environment
  • Excellent collaboration, communication and presentation skills
 

Do not waste any minutes, apply now!  We are looking forward to receiving your application. 

Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.