Senior Vice President, Technical - Clinical Regulatory Affairs

ComplianceComplianceFull TimeRemoteSeniorTeam 10,001+Since 1983H1B SponsorCompany SiteLinkedIn

Location

United States

Posted

1 day ago

Salary

0

Seniority

Senior

Postgraduate Degree15 yrs expEnglish

Job Description

Senior Vice President, Technical - Clinical Regulatory Affairs

Parexel

• Work on a variety of assignments, diverse product types for clients • Creating opportunity for clients throughout the product lifecycle • Sharing scientific, technical, regulatory, and/or commercial expertise • Leading teams of respected SMEs • Meeting new situations and learning • Provide mentoring and guidance to other RS employees

Job Requirements

  • MD or PhD required
  • 15+ years experience with expert level industry or regulatory knowledge experience in Clinical Development/Clinical Trial Design, Clinical Strategy, and authoring clinical sections of regulatory applications
  • Previous experience with a regulatory agency (such as the FDA or MHRA) as a Senior / Master Medical Review Officer, Team Lead, etc. or a related Medical role is strongly preferred
  • Extensive Neuroscience, Rare Disease, Immunology, Endocrinology/Metabolism experience is highly preferred
  • Ability to travel up to 20-30% domestically and/or internationally may be required for Client and/or Health Authority Meetings and Thought Leadership/Conference Attendance

Benefits

  • Work from home
  • Opportunity to influence development strategies

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