global study manager in Basel

posted
contact
Barbara Sorce, 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
15388
contact
barbara sorce, basel professionals health care & life sciences
phone
058 201 55 50

job description

Our client a pharmaceutical company in Basel is looking for a Global Study Manager Start date: ASAP or max March 2021Length: 1 year with possibility of extensionRemote/Home Office: Fully home office atm due to Covid-19 Background:The perfect candidate has a strong level of broad experience in running trials from the operational aspect (vendors, affiliate or CRO management, team work (and some budget experience useful). Also, the candidates need to be able to start working on studies immediately, there won't be much time for 'getting used to the work environment' etc. As a Global Studies Manager (GSM) you will lead or contribute to one or more cross-functional global working groups, expert squads, and global Study Teams, which deliver all operational aspects of one or more studies through all phases and stages.
  • DRIVE OPERATIONAL EXCELLENCE by developing operational plans, creating and managing clinical study budget and overseeing the consistency of operations
  • MANAGE VENDORS AND STAKEHOLDERS by managing relationships with vendors and cross-functional stakeholders. Oversee performance of vendors and third-party providers
  • LEAD AND INFLUENCE by establishing yourself as a leader within the team, being recognized as a thought leader who inspires others to perform at their best and learn from best practices. You’ll be shaping our capabilities and evolving your role overtime
  • MANAGE RISK AND COMPLIANCE by developing site monitoring and risk mitigation strategies and ensuring your team adheres to all appropriate standards, including ICH/GCP and other regulations
  • PLAN DEMAND AND SUPPLY by overseeing the resource management, forecast and maintenance of supplies needed to ensure sites have the necessary supplies to run clinical studies
  • PROVIDE COUNTRY OVERSIGHT by leading feasibility assessments to ensure countries and sites are selected for participation in trials. Provide guidance to country operational reps during trials
You will succeed as a Global Studies Manager by leading, collaborating, and relaying your expertise to cross-functional partners.
  • Apply your good knowledge of drug development process and respective regulations, including ICH and GCP guidelines
  • Apply your organizing and problem-solving skills to plan and run efficient operational aspects of a study
  • Motivate others to deliver against commitments, including leadership of global teams across diverse cultures and time zones to ensure successful collaboration
  • Demonstrate agility and ability to perform in a highly fast-paced, matrix environment where cross-team collaboration is crucial
  • Leverage excellent verbal and written communication skills to motivate your team, negotiate with peers and partners and influence across stakeholders
Must haves:
  • Minimum of 3/4 years in clinical trial management (*****)
  • Possess strong working knowledge of drug development process and respective regulations, including ICH and GCP guidelines (*****)
  • Minimum Bachelor's Degree in Life Sciences (*****)
  • Have a growth mindset and are excited about learning through experience
  • Feel comfortable thinking on your feet and thrive in fast-paced, ambiguous and highly collaborative environments
  • A self-starter who finds passion in achieving successful outcomes by leading, directing and inspiring peers
  • Want to make a difference and find excitement in innovating practices, products and processes
Nice to haves:
    • Immunology and/or neuroscience experience (***)
    • Budget management and oversight (**)