ON BEHALF OF BIOGAIA AB WE ARE RECRUITING A CLINICAL RESEARCH MANAGER, CRM.

In this role, you will be responsible for designing, implementing, and monitoring clinical studies in line with BioaGaia’s Discovery and Research clinical strategy. You will manage these studies according to project plans and collaborate closely with CROs and/or principal investigators. Additionally, you will ensure timely achievement of key milestones, including scoping of clinical studies. To succeed in the position, you should bring an innovative, proactive, problem-solving, and collaborative mindset.
About the company: BioGaia is a Swedish world-leading probiotics company that has been a pioneer in microbiome research for over 30 years. BioGaia’s products, based on L. reuteri bacterial strains, are among the most scientifically validated globally. BioGaia develops, manufactures, markets, and sells clinically proven probiotic products for gut, oral, and immune health. The products are sold through distribution partners and through their own distribution in over 100 countries. The BioGaia Group has around 210 coworkers and operate in three geographical markets: EMEA, Americas, and APAC. The class B share of the Parent Company BioGaia AB is quoted on the Mid Cap segment of Nasdaq Stockholm.
Read more: https://www.biogaia.com/

EXPERIENCE & SKILLS

• Life Science M.Sc /PhD (Microbiology, Cell Biology, Biochemistry, etc.) with a strong focus on clinical evaluation of probiotics or other ingredients, -or Medical Degree in related areas.
• 5+ years professional experience in a relevant industrial/company environment.
• Medical practice or background highly appreciated.
• Strong knowledge of clinical studies from design to implementation: willing to collaborate with medical investigators and to secure clinical study follow-up.
  The role reports to Clinical & Scientific Affairs Director.

• Design, implement and perform clinical trials for BioGaia, according to established Research Programs.
• Contribute to the clinical strategy of the company, as well as designing and managing clinical studies at the scientific and operational levels.
• Contribute to the writing of the study protocols, to discussions with principal investigators and other experts and to the scientific and budget follow-up.
• Contribute to the scientific publication of the studies.
• Communicate clinical project status and results.
• Be proactively involved in managing the clinical investigators network as well as analyzing and interpreting the data obtained.
• Perform other duties in line with the position as assigned by the company.