Development Clinical Research Physician - Neuroscience Medical Director
Cork, Ireland – hybrid work model
Overview:
Through the application of scientific and medical training, clinical expertise, and relevant clinical experience, the Development Clinical Research Physician (CRP) participates in: the development, conduct, and reporting of corporate/global clinical trials in support of registration and commercialization of the product; the implementation of global clinical trials; the reporting of adverse events as mandated by corporate patient safety; the review process for protocols, study reports, publications and data dissemination for products, new and updated labels, documents and tools supporting product pricing, reimbursement, and access (PRA), grant submissions and contracts; contacts with regulatory and other governmental agencies; outreach medical activities aimed at the external clinical customer community, including thought leaders; the development and implementation of the business unit and global strategy for the product; and various medical activities in support of demand realization. The CRP serves as a scientific resource for study teams, departments, and others as needed. The clinical research scientist serves as a scientific resource for study teams, departments, and others as needed.
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The Clinical Research Physician must be aware of and ensure that all activities of the medical team comply with current local and international regulations, laws, guidance (for example, FDA, ICH, CPMP, etc.), Good Clinical Practices (GCPs), company standards, policies and procedures, company integrity agreements as applicable, and the Principles of Medical Research and activities are aligned with the medical vision. The primary responsibilities of the Development CRP are generally related to late-phase and marketed compounds.
Medical Doctor or Doctor of Osteopathy:
- Physicians must have completed education and training at a medical school that meets the requirements of the US Liaison Committee on Medical Education (LCME).
- US-trained physicians (Medical Doctors or Doctors of Osteopathy) must have achieved board eligibility or certification in Neuroscience.
- Previous people management experience
- Demonstrated knowledge of the drug development process
- Demonstrated ability to influence others (both cross-functionally and within the function) to create a positive working environment.
- Ability to engage in domestic and international travel to the degree appropriate to support the business of the team.
Additional Skills/Preferences
- Clinical research or pharmaceutical medicine experience preferred
- 5 years of work experience in Neuroscience
- Minimum of 5 years of professional experience in pharmaceutical drug development with demonstrated experience and knowledge of clinical research and the drug development process.
Job Types: Full-time, Permanent contract
Benefits:
- Housing allowance
- Profit sharing
- Wellness program
Schedule:
- Monday to Friday
Supplemental pay types:
- Bonus pay
- Yearly bonus
Work Location: In person
