Global Clinical Trial Lead & Study Manager

Merck

New Jersey

On-site

USD 140,000 - 190,000

Full time

4 days ago
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Job summary

Merck is seeking an experienced clinical operations leader to drive strategy and oversee planning and execution of clinical trials. You will lead a global, cross-functional team and coach staff in project management, communication, and collaboration to meet study objectives.

Coordinate with study teams, vendors, and country partners; ensure GCP/ICH compliance and present milestones to senior management. A life sciences degree with 9+ years in pharma clinical development is required, or a

Qualifications

  • Bachelor's degree with 9+ years of pharmaceutical/clinical drug development experience
  • Master's degree with 6+ years of pharmaceutical/clinical drug development experience
  • PhD/PharmD with 2+ years of pharmaceutical/clinical drug development experience

Responsibilities

  • Lead operational planning, feasibility, execution and conduct of clinical trial(s)
  • Serve as the Clinical Trial Team (CTT) lead
  • Direct teams in study planning, development, and execution elements (operational reviews, issue escalations, governance)
  • Collaborate with internal/external stakeholders (study team, country teams, vendors) to support trial objectives
  • Liaise with partners, vendors, and vendor management team
  • Review clinical documents for input (protocols, etc.)
  • Possibly serve as SME on process improvement teams
  • Build talent and capabilities through coaching and development; may manage reports

Skills

Leadership
Clinical Operations
Regulatory Knowledge (GCP/ICH)
Project Management
Strategic Thinking
Communication Skills
Stakeholder Management
Problem Solving
Analytical Thinking
Microsoft Office

Education

Bachelor's Degree in Life Sciences
Master's Degree in Life Sciences
PhD/PharmD in Life Sciences

Job description

Merck is seeking an experienced clinical operations leader to drive strategy and oversee planning and execution of clinical trials. You will lead a global, cross-functional team and coach staff in project management, communication, and collaboration to meet study objectives.

Coordinate with study teams, vendors, and country partners; ensure GCP/ICH compliance and present milestones to senior management. A life sciences degree with 9+ years in pharma clinical development is required, or a

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