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Contract Senior Manager, Global Trial Optimisation
- Contract
- Clinical Research Associate (CRA)
- United Kingdom
This vacancy has now expired. Please see similar roles below...
Proclinical is seeking a dedicated Manager of Global Trial Optimisation. This role involves overseeing the clinical development strategy, clinical study concepts and protocols as well as operational plans. The successful candidate will play a crucial part in maintaining relationships with external experts to facilitate a wide source of country and disease area intelligence that can be utilised in study design and operational planning.
Responsibilities:
- Lead study level feasibility processes to inform study design, optimal geographical placement, and operational planning.
- Partner with teams during CRO led feasibility activities to support validation of study and country level enrolment rates and study start-up timelines.
- Support the development and implementation of the Global Trial Optimization function through process initiatives and change management activities.
- Partner with Data and Analytics function to review and identify appropriate central data sources.
- Lead study level engagements to obtain, analyze and deliver high-quality targeted information from external stakeholders.
- Lead study level activities to generate and deliver patient level insights.
- Provide input into a range of continuous improvement activities to ensure consistency of Global Trial Optimization process execution.
- Partner with study teams to develop and implement patient recruitment and retention tactics aligned with defined study strategy.
Key Skills and Requirements:
- Exceptional interpersonal & leadership skills.
- Expert knowledge and a data-driven approach to planning, executing, and problem-solving.
- Advanced communication skills via verbal, written, and presentation abilities.
- Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization.
- Ability to influence and negotiate across a wide range of collaborators.
- Knowledge of ICH/GCP and regulatory guidelines/directives.
- Advanced project management skills, cross-functional team leadership, and organizational skills.
- A minimum of a Bachelor's degree and relevant industry experience.
- Direct experience managing global clinical trial operations, including experience developing protocols and key study documents.
- Technical proficiency in trial management software and MS applications.
Interested or know someone who might be? Reach out to Matthew Pike using the following:
📞 +44 207 4400 639 (5342)
Apply Now:
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. is acting as an Employment Agency in relation to this vacancy.
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