Senior Medical Director Consultant

5 days ago

San Diego, California, United States Meet Recruitment Inc. Full time

We are seeking a highly skilled Senior Medical Director Consultant to join our team at Meet Recruitment Inc. as a 20-hour per week consultancy role. Reporting to the Chief Medical Officer, this position involves supporting clinical leadership and ensuring the successful design and implementation of Clinical Development Plans.

**Key Responsibilities:**

  • Develop and Maintain Clinical Development Plans: Collaborate with cross-functional teams to design and implement clinical development plans that meet regulatory requirements and drive business growth.
  • Design Clinical Trials and Review Critical Study Documents: Utilize expertise in respiratory diseases to design clinical trials and review critical study documents, including Investigator Brochures and IND submissions.
  • Lead Project Team Meetings and Manage Actionable Minutes: Facilitate project team meetings, manage actionable minutes, and ensure effective communication among team members.
  • Participate in Strategic Decision-Making: Contribute to strategic decision-making processes, providing medical and scientific expertise to inform business decisions.
  • Engage with External Advisors, Thought Leaders, and Internal Teams: Collaborate with external advisors, thought leaders, and internal teams to execute the drug development plan and drive business growth.
  • Maintain Medical/Scientific Standards and Educate Team Members: Ensure that medical and scientific standards are maintained, and educate team members on best practices and regulatory requirements.
  • Participate in Management and Oversight Committee Meetings: Participate in management and oversight committee meetings, providing medical and scientific expertise to inform business decisions.
  • Interact with Regulatory Agencies and Represent Projects to Partners and Investors: Interact with regulatory agencies, represent projects to partners and investors, and ensure compliance with regulatory requirements.

**Requirements:**

  • Advanced Degree (MD) with Experience in Cystic Fibrosis: Possess an advanced degree (MD) with experience in cystic fibrosis, preferably with board certification in respiratory medicine or medical genetics.
  • 8+ Years of Clinical Research Experience in the Pharmaceutical Industry: Have 8+ years of clinical research experience in the pharmaceutical industry, with expertise in clinical trial design, implementation, and sponsor/site interactions.
  • Understanding of Rare Disease Drug Development: Possess a deep understanding of rare disease drug development, including clinical trial design, implementation, and regulatory requirements.
  • Proven Leadership Experience in Development Project Teams: Demonstrate proven leadership experience in development project teams, with the ability to manage cross-functional teams and drive business growth.
  • Excellent Communication Skills, Including Writing and Presentation: Possess excellent communication skills, including writing and presentation, with the ability to effectively communicate with internal and external stakeholders.
  • Strong Business Acumen and Ability to Align Teams with Corporate Strategy: Demonstrate strong business acumen and the ability to align teams with corporate strategy, driving business growth and ensuring compliance with regulatory requirements.

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