Regional Medical Director

**MUST HAVE PHARMACEUTICAL, BIOTECHNOLOGY, MEDICAL AFFAIRS OR CLINICAL EXPERIENCE!**

Our client is a specialty biopharmaceutical company focused on the development, manufacturing, sales and marketing of biopharmaceutical products. Their areas of focus include neurology, pain and physical medicine/rehabilitation. They are a performance-driven company that is committed to creating a diverse workforce and building a culture based on working together to deliver high-quality products and exceptional service.

Responsibilities:
• Participate in Clearance Committee review process.
• Participate in Grant and Protocol Review Committee.
• Participate in setting publication strategy.
• Medical resource for reimbursement and customer relations group.
• Medical Safety Monitor for registry, phase II-IV studies.
• Review adverse event and other reports generated by the pharmacovigilance group.
• Resource for medical information group (e.g., assistance with abstract and publication analysis, review standard response letters and respond to specific questions).
• Resource for medical science liaison (MSL) group (e.g., meet with thought leaders, participate in educational and market research dinner meetings, conduct advisory boards, present product-specific clinical data for P&T review, provide education on botulinum toxins, injection techniques, dystonia, spasticity, and other allied conditions; and similar activities for any additional products acquired or promoted by the company.
• Consultant to Investigators, CROs and MSL team re: protocol and CRF design.
• Product and therapeutic area medical contact for outside agencies; work with Regulatory on FDA communications and submissions.
• Strategic Planning with Sales and Marketing on product life cycle management.
• Represent Medical Affairs in preclinical and phase I development group efforts.
• Resource to Manufacturing on medical/scientific issues.

Additional activities
• Business Development: analyze acquisition or copromotion targets.
• Knowledge and skill set enhancement: US FDA Regulatory (e.g., cGMP, GCP, GLP, DDMAC) and other Regulatory authorities; medical statistics; clinical trial design and conduct; leadership and management.
• Career Path Development
REQUIREMENTS
Qualifications:
• An MD or doctoral degree in Neurology or Physiatry
• Industry experience in a medical affairs or clinical research role.
• Must have excellent communication skills, strong interpersonal skills and the willingness to travel as frequently as needed.
• Must be a clear and focused thinker with a strong clinical research background, and excellent problem solving abilities.
• Must be able to multi-task and deliver exceptional work product in a timely fashion.