Clinical Study Lead – UK – Permanent

CSL

Job Type: permanent
Job Category: Clinical
Region: United Kingdom
Area: England
Location: Unspecified
Salary: Competitive
Posted: 29th November 2021
Ref: CSLHLIO

As a Clinical Study Lead (CSL), you will lead the cross-functional study team responsible for the global execution of smaller, less complex clinical trials from study design through study close out. These responsibilities apply to both internally sourced studies and studies outsourced to CROs, so we need a CSL who has experience managing Third-Party Vendors. We need someone who can also contribute to and drive process improvement initiatives that support our rapidly growing organization. This is an exciting time to join our organization and have a direct impact on bringing life-saving treatments to the market.

As a Clinical Study Lead, a typical day might include the following:

  • Providing operational input into protocol development
  • Leading all aspects of and contributing to the development of study specific documentation e.g. case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc.
  • Supervising set-up and maintenance of study systems such as Clinical Trial Management System (CTMS), Trial Master File (TMF) etc.
  • Ensuring compliance with the clinical trial registry requirements
  • Providing input into baseline budget and timeline development and managing the study against planned budget, timeline and results
  • Leading risk assessment and identifies risk mitigation strategies at the study level
  • Managing feasibility assessment to select relevant regions and countries for the study
  • Conducting site evaluation and selection
  • Leading investigator meeting preparation and execution
  • Monitoring progress for site activation and monitoring visits and acts on any deviations from plan
  • Managing development and implementation of patient recruitment and patient retention strategies
  • Monitoring data entry and query resolution and taking action on any divergence from agreed metrics
  • Overseeing and providing input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation
  • Raising issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other partners and developing and implementing appropriate actions to address issues
  • Ensuring data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations, and suspected serious non-compliance by sites
  • Ensuring clinical project audit and inspection readiness through the study lifecycle and contributing to CAPAs as required
  • Supervising study close-out activities and contributing to clinical study report writing and review
  • May include direct supervision of CTM staff including assigning work, performance management, recruitment, coaching and professional development.

This role might be for you if:

You have direct management experience with demonstrated results building and developing outstanding teams

You have the capacity to understand and implement the strategic direction and guidance for respective clinical studies

You can take a proactive and self-disciplined approach to managing projects with a developed ability to meet deadlines and prioritize

You have a history of effectively leading and negotiating with vendors

You have a data-driven approach to planning, executing and problem solving

You operate with a high degree of cross-functional agility using exceptional influencing and interpersonal skills

You have the innate ability to rally disparate groups to accomplish lofty shared goals

To be considered for this opportunity you must possess a Bachelors’ degree with a minimum of 6 years of relevant industry experience. Advanced degrees may be considered in lieu of relevant experience. Direct experience managing global clinical trial operations is a must, including experience developing protocols and key study documents. You will also need technical proficiency with trial management software and MS applications to be considered.

GET IN TOUCH TO KNOW MORE
E: Hirons@barringtonjames.com

T: +441293 776644

LI: https://www.linkedin.com/in/helaina-irons-351670195/?senderId=suky-sandhu-629691144

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