Clinical Project Physician


Basel Stadt

About Idorsia Pharmaceuticals Ltd


Idorsia Ltd is reaching out for more - We have more ideas, we see more opportunities and we want to help more patients.

In order to achieve this, we want to develop Idorsia into one of Europe’s leading biopharmaceutical companies, with a strong scientific core.

Headquartered in Switzerland - a European biotech hub - Idorsia is specialized in the discovery and development of small molecules, to transform the horizon of therapeutic options. Idorsia has a broad portfolio of innovative drugs in the pipeline, an experienced team, a fully-functional research center, and a strong balance sheet – the ideal constellation to bringing R&D efforts to business success.

Idorsia was listed on the SIX Swiss Exchange (ticker symbol: IDIA) in June 2017 and has over 1,000 highly qualified specialists dedicated to realizing our ambitious targets.


Main requirements:


  • Medical Doctor degree.
  • At least  3 years experience in clinical research in a clinical research organization (CRO) or Pharmaceutical Company.  
  • Demonstrated experience in overseeing clinical projects from a medical perspective.
  • Sound knowledge of drug development based on previous deliverables.
  • Clinical research experience across mutiple area (e.g. CNS, nephrology, metabolic diseases).
  • Clinical research experience in pediatric indications would be an advantage.


Main tasks: 


  • Overall the CPP is responsible for providing medical leadership, oversight and guidance on clinical development projects under his/her responsibility from. concept generation to design, implementation, execution, and submission/approval.
  • Contribute to global strategic development and provide evidence-based input to the clinical project. 
  • Deliver the medical components of the Clinical Development Plan (CDP) related to the project indication(s).
  • Provide medical input to the project-related communication/publication plan.
  • Develops and maintains interactions with key external experts and Investigators. 
  • Lead medical aspects of clinical advisory boards and study specific committees.
  • Contribute to clinical/scientific content for submissions to regulatory agencies and IRBs/ethics boards.
  • Be the company clinical expert at key regulatory interfaces, investigator meetings, patient organization meetings.
  • Contribute as needed to clinical trial level medical activities.

Work  Location: Basel Area - Allschwil

Country: Switzerland

Business Area: Global Clinical Development

Schedule: Fulltime

Job Type: Permanent

Job ID: 3346


If you are interested, please click on apply now.

Please be informed that if you are selected for this position, your employment will be subject to a pre-employment background screening process, of which you would be informed in greater detail in due course.

Please note Idorsia operates a strictly controlled list of preferred recruitment partners. For those partners who have no valid, signed Master Service Agreement in place with Idorsia, all unsolicited resumes, CVs, anonymous profiles, or any other candidate details submitted through our website or to personal e-mail accounts of employees of Idorsia Pharmaceuticals (including any of its subsidiaries, affiliates, or related companies) are considered the property of Idorsia Pharmaceuticals and are not subject to payment of any form of introduction, placement or referral fees.