Position: Associate

Job type: Full-time

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Job content

Hobson Prior are seeking for a Clinical Project Physician to join a fantastic pharmaceutical organisation on a contract basis located in Allschwil. Our client is focused on generating healthier societies around the world.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities
  • You will be responsible for contributing to and is a significant member of clinical study team.
  • Performs medical data analysis of trial data, involving eligibility review.
  • Accountable for site interactions in partnership with the SRS for medical questions and education (including safety management guidelines).
  • For the role of Clinical Project Physician, you will be responsible for the evaluation of key safety-related serious adverse events in partnership with the Local Safety Officer and the Medical Safety Officer and supervises safety narratives.
  • Co-operates with the SRS and inputs into protocols, offering medical strategic supervision in protocol development (input on inclusion/exclusion criteria and other safety-related clinical considerations).
  • Work alongside with the leadership and other cross-functional team members, implements CDP, designs and develops clinical plans and protocols with a strong tactical focus.
  • You may occasionally lead study Steering Committees (mutually with Clinical Leader).
  • Might add to IDMC (selection of members, drafting of charter, etc.).
  • The ideal candidate will direct the examination of benefit/risk for clinical study protocols in a matrix team setting working in partnership with SRS.
  • Associate with CS to support executional distribution of studies (e.g., site activation, enrolment status, as well as adjudication for protocol violations, significant, non-significant deviations, etc.).
  • Any other assigned duties.
Requirements
  • Required to have obtained a Medical Degree.
  • At least 5 years of industry and previous experience with clinical development/clinical studies is preferred but not essential.
  • Clinical experience in cardiology or pulmonology area is highly preferred.
  • Past experience handling projects with clinical trials involving development of protocols, case report forms, informed consent, study initiation, protocol training, and clinical data monitoring is ideal.
  • Exceptional written communication, oral communication, and presentation skills are essential to the role.
  • The individual must have established ability to operate and direct in a cross-functional and matrix team setting, functioning with external investors and be flexible and adaptable.
Apply Now

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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Deadline: 09-05-2024

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