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Regional Site Advocate - East Coast
at Vertex
Boston, MA

Regional Site Advocate - East Coast
at Vertex
Boston, MA

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Description

Job Description:


Vertex is hiring Regional Site Advocates (RSA) in the US. This role is tasked to help transform the Clinical Research site experience with Vertex by making the customer a priority. The Regional Site Advocate is an externally facing position that acts as a critical interface between Vertex and Clinical Research sites for all operational issues.

Key Responsibilities:
  • Serve as a professional, competent and reputable Vertex representative in direct interaction with clinical trial investigators and academic institutions on all activities related to study execution
    • Dedicated to serving as the key point of contact for sites for any operational issues that are not rapidly resolved through established pathways
    • Establish continuity for sites involved in multiple studies/programs
    • Navigate within Vertex and vendors to identify root cause and to expedite resolution of the issues
  • Actively develop and maintain positive working relationships with Clinical Research site personnel; conduct routine and as needed site visits
  • Identify opportunities for process improvements to achieve better results in study execution
  • Represent regional insight and interests in country/site selection activities
  • Partner with the Medical Science Liaison, identify new sites and assess capabilities for participation in Vertex clinical studies
  • Ensure training new sites on Vertex protocols/processes/systems, potentially including GCP training for research naive sites
  • Anticipate and escalate site specific challenges and requirements and proactively communicate to the team to plan and mitigate risks
  • Contribute to knowledge repository for site /country specific information related to study execution
  • Partner with other RSAs globally to achieve industry leading performance
  • Stay abreast of regulations and industry trends and proactively prepare to maintain compliance
  • Leverage in-depth understanding of local regulations and trial implementation pathways to ensure streamlined site start-up
  • Ensure seamless internal communication between Clinical Development and Regional Medical Affairs Team
This is not an exhaustive, comprehensive listing of job functions. Other duties may be performed as assigned. Travel may be required up to 50% of time.

Key Competencies Required:
  • Outstanding collaboration skills
  • Self-motivated and ability to work well independently and in a team environment
  • Excellent verbal and written communication
  • Excellent critical thinking and problem solving skills

Qualification:

Minimum Qualifications:
  • Bachelor's degree with a major in a related field and at least 5 years of Clinical Development experience
  • Proven track record of management of long-term professional relationships (e.g. Clinical sites)
  • Must have good working knowledge of ICH, FDA, IRB/IEC and other applicable regulations/guidelines and significant experience with Clinical Site start-up documents
  • Medical background or experience in Vertex Therapeutic Areas a plus
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