Join Us

Our team is dedicated to the preclinical and clinical development of novel pharmacotherapies to treat disorders of the inner ear with high unmet medical need. Because our employees are the key to our success, we carefully select each new member of the team. We seek colleagues who perform their work with knowledge and dedication, who value integrity and who take initiative both within a team and individually.

Does finding a new job in Berlin, the vibrant capital of Germany, sounds like the perfect next step for you? Are you enthusiastic about making a difference in the lives of people with acute hearing disorders? Would you like to become part of an energetic team of inspired and highly skilled professionals? Then we invite you to explore AudioCure´s current job positions.

We are currently recruiting. Please see the link below for your opportunity to join the AudioCure team (information on the application process can be found in the separate privacy policy for applicants):

Senior Clinical Research Associate (CRA) m/f/d

What AudioCure offers

We are an innovative, young pharmaceutical company based in Berlin Mitte. We develop drugs with high medical need, especially for hearing loss, tinnitus and neurodegenerative diseases.

As part of a highly motivated team, you will have the opportunity to get to know, advance and actively shape the development of promising drugs from the synthesis of active ingredients and formulation development to preclinical and clinical testing of tolerability and efficacy.

These are your main tasks

  • You are the key contact person from the sponsor side for the Clinical Operations Team (CPLs, CRAs) of our CROs and ensure the support of international study centres in compliance with the protocol, regulatory requirements and GCP guidelines
  • Under your guidance, our CROs will search for new study centres. You will support the preparation and evaluation of feasibility studies
  • Review and follow-up of monitoring reports
  • Organising the purchase and dispatch study materials and documents
  • Create and maintain study-specific trackers and lists

What you bring with you

  • Degree in the natural sciences (e.g. biology, biochemistry, medicine, pharmacy, chemistry) or equivalent training
  • Several years of practical experience as a (senior) CRA in the supervision of clinical trials, especially international and early phase trials (on-site monitoring)
  • Experience in cooperation with study centres, CROs and stakeholders
  • Experience in preparing/reviewing regulatory and study documents (e.g. ICF, monitoring reports, investigator site file, responsibility and training logs, etc.)
  • Willingness to travel occasionally (also internationally), e.g. to motivate study centres, accompany auditors or study CRAs
  • Proficiency in written and spoken English (business fluent)
  • Creativity, motivation, team-player attitude, and good communication skills

The following knowledge is also desirable

  • Experience with otological indications / studies
  • Experience with regulatory submissions
  • Experience in quality management e.g. creation/review of SOPs
  • Good written and spoken German

Please send your CV including cover letter to: careers@ac-clinical.com