Associate Director, Clinical Trial Lead (all genders)

TN United Kingdom; Greater London; On-site; GBP 60,000 - 100,000; Full time

Job summary

An established industry player is seeking an Associate Director, Clinical Trial Lead to oversee complex clinical studies and projects. This role requires a seasoned professional with extensive experience in clinical trial management, demonstrating leadership and strategic vision. You will manage large global project teams, ensuring successful execution of clinical trials while adhering to budget and quality standards. The ideal candidate will possess strong interpersonal skills to foster partnerships across multidisciplinary teams and drive innovation in clinical operations. If you have a passion for advancing clinical research and a proven track record in the pharmaceutical industry, this opportunity is for you.

Qualifications

• 10-12 years in clinical research with 7 years in clinical trial management.
• Experience in oncology and immunology preferred.

Responsibilities

• Manage multiple complex studies and projects, ensuring timely execution.
• Lead clinical trial strategy development and project delivery.

Skills

Clinical trial management

Project management

Leadership

Stakeholder management

Risk assessment

Education

Advanced degree (MPH, MS, MA, MBA, PharmD)

Job description

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

Client: [Client Name]

Location: Feltham, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: 1e428dd1b8a7

Job Views: 10

Posted: 02.04.2025

Expiry Date: 17.05.2025

Job Description:

Your role includes managing multiple studies, projects, and work streams with high complexity, risk, impact, and reach, typically Ph III and registrational/sourcing models. You will demonstrate skills in successfully leading large-sized global project teams in a matrix organization and direct, influence, and motivate stakeholders from closely related areas and beyond, creating a positive working climate.

You will lead the development of the clinical trial strategy while being accountable for successful project execution and delivery of clinical operational budget, timelines, and quality standards agreed upon by Governance Committees. As a core member of the Clinical Operations Team and leader of the Clinical Trial Team, you will align the clinical trial team with organizational goals, Clinical Operations Team, and/or Global Program Strategy Team.

You will filter, prioritize, analyze, and validate complex and dynamic information from a diverse range of external and internal sources to respond to operational and organizational challenges in a holistic manner to mitigate risks. You will exhibit Subject Matter Expert level understanding of multiple functions and functional processes, remaining familiar with and considering overall company strategy.

You will act as a senior advisor and mentor within the team and beyond, serving as a best practice resource within your discipline or as a technical functional team or project. Ensure all study management activities are completed in accordance with SOPs/WI, local regulatory guidance including ICH-GCP; audit leadership- interviewee & responses. You will contribute to non-study related initiatives in addition to study assignments and provide reports to senior management, including updates and timelines independently.

You will demonstrate creativity and innovation to support projects from a strategic perspective, able to predict the result of action in advance and achieve goals.

Who you are:

At least 10-12 years in clinical research in a CRO or Pharmaceutical/Biotechnology Industry environment with at least 7 years of in-depth experience in clinical trial management including managerial responsibility. An advanced degree is desirable (MPH, MS, MA, MBA, PharmD); PM cPMP is desirable. Proven experience in all aspects of clinical study planning and startup (including budget and resource planning) and in executing study activities, from startup through final study report.

Experience in multiple Therapeutic Areas (oncology and immunology preferred) is required, along with substantial to extensive professional experience in relevant disciplines and substantial project management experience. Strong leadership competencies and influencing skills are necessary, as well as proven team dynamic knowledge and skills and the ability to foster partnerships across projects and multidisciplinary teams. A growing expertise in drug development, including some knowledge of interfaces and interdependencies of clinical development with other nonclinical & pharmaceutical development, regulatory, and commercial/marketing is also required.

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Created on 02/04/2025 by TN United Kingdom