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
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