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Associate Director, Clinical Trial Liaison (Field Based)

8+ years
$156,000 - $234,000
10 Nov. 14, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Trial Liaison (CTL) / Associate Director

Company: Vertex Pharmaceuticals

Location: Remote-Eligible

Position Overview:

Vertex Pharmaceuticals is seeking a Clinical Trial Liaison (CTL) or Associate Director to enhance the clinical research experience by focusing on customer relations and driving operational excellence in clinical trial execution. The CTL role serves as a strategic liaison between Vertex and clinical research sites, handling site outreach, specialized training, and ensuring effective site engagement throughout the trial lifecycle. This role is crucial for fostering relationships with clinical trial investigators, academic institutions, and therapeutic networks while ensuring regulatory compliance and driving efficient site selection and performance.

Key Responsibilities:

  • Act as a primary contact and representative for Vertex in interactions with clinical trial investigators and research sites during feasibility, site selection, and trial execution.
  • Identify and recruit new sites and engage therapeutic area networks to increase trial success.
  • Influence clinical research culture, ensuring the inclusion of diverse investigators from underrepresented communities.
  • Collaborate with study teams to identify opportunities for process improvement and deliver feedback to optimize study outcomes.
  • Participate in site selection and decision-making processes, representing regional insights and interests.
  • Provide specialized training to clinical sites and investigators on the investigational product and study design.
  • Monitor and report on site performance using Key Performance Indicators (KPIs).
  • Ensure compliance with local regulations and guide streamlined site startup processes.
  • Manage external relationships with clinical sites and therapeutic area networks, enhancing communication and collaboration.
  • Lead or support teams as necessary, with potential oversight responsibilities for team members.
  • Travel up to 50% as required by the role.

Required Qualifications:

  • Bachelor’s degree (or equivalent).
  • 8+ years of experience in Clinical Development, with at least 2 years of management or supervisory experience.
  • Strong working knowledge of ICH, FDA, EU-CTR, IRB/IEC, and clinical site start-up regulations.
  • Proven track record in managing professional relationships with clinical research sites.
  • Experience with Vertex Therapeutic Areas is a plus.
  • Fluent in English; additional language skills are an asset.

Compensation:

  • Base Salary: $156,000 - $234,000 (depending on experience and qualifications).
  • Eligible for annual bonus and equity awards.
  • Comprehensive benefits package, including medical, dental, vision, paid time off, and 401(k) match.

Flex Designation:

  • Remote-Eligible: Work remotely up to five days per week with occasional on-site visits, or select hybrid/onsite options per Vertex's Flex @ Vertex policy.

Application Process:

To apply, please submit a cover letter, CV, and references via Vertex’s careers portal. For accommodations or further assistance during the application process, contact Talent Acquisition at ApplicationAssistance@vrtx.com.

Vertex is an equal opportunity employer, committed to diversity and inclusion, and welcomes applicants from all backgrounds.

Posting Status:

  • Posting Date: Ongoing
  • Position Type: Full-Time
  • Travel Requirement: Up to 50%
  • Location Flexibility: Remote-Eligible