Associate Director, Clinical Trial Lead (all genders)

Merck KGaA, Darmstadt, Germany; London; On-site; GBP 80,000 - 120,000; Full time

Job summary

A leading company in the pharmaceutical sector seeks an Associate Director, Clinical Trial Lead to manage complex clinical studies and mentor project teams. The ideal candidate will have extensive experience in clinical trial management, strong leadership skills, and a background in oncology or immunology. Join us to drive innovation and ensure compliance in clinical development.

Qualifications

• 10-12 years in clinical research; 7 years in trial management.
• Advanced degree preferred; PM cPMP certification desirable.
• Experience in oncology and immunology preferred.

Responsibilities

• Manage multiple complex studies and projects.
• Lead global project teams in a matrix organization.
• Develop clinical trial strategies and project execution.

Skills

Leadership

Project Management

Influencing Skills

Risk Analysis

Team Collaboration

Education

Advanced degree (MPH, MS, MBA, PharmD)

Job description

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Associate Director, Clinical Trial Lead (all genders), Feltham

Location: Feltham, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference:

1e428dd1b8a7

Job Views:

4

Posted:

02.06.2025

Expiry Date:

17.07.2025

Job Description:

Your role:

• Manages multiple studies, projects, and work streams with high complexity, risk, impact, and reach, typically Phase III and registrational/sourcing models.
• Leads large global project teams in a matrix organization, influencing and motivating stakeholders to create a positive working climate.
• Develops clinical trial strategies and ensures successful project execution within budget, timeline, and quality standards.
• Aligns clinical trial team with organizational goals and global strategies.
• Analyzes complex information to respond to operational and organizational challenges, mitigating risks.
• Acts as Subject Matter Expert in multiple functions, considering overall company strategy.
• Serves as a senior advisor and mentor, sharing best practices.
• Ensures study activities comply with SOPs, local regulations, and ICH-GCP, including audit leadership.
• Contributes to non-study initiatives and reports to senior management.
• Supports strategic projects through creativity and innovation.

Who you are:

• 10-12 years of clinical research experience in CRO or Pharma/Biotech, with at least 7 years in clinical trial management and managerial responsibility.
• Advanced degree preferred (e.g., MPH, MS, MBA, PharmD); certifications like PM cPMP desirable.
• Experience in study planning, startup, and execution across multiple therapeutic areas (oncology and immunology preferred).
• Strong leadership, influencing skills, and project management experience.
• Ability to foster partnerships across multidisciplinary teams.
• Growing expertise in drug development and understanding of clinical development interfaces.