Director of Clinical Operations

3 weeks ago


UK, UK, United Kingdom Meet Full time

My client is seeking an accomplished Director of Clinical Operations to lead their clinical research team within a dynamic, industry-leading organization at the forefront of medical innovation. This pivotal role offers an opportunity to go beyond traditional oversight responsibilities by driving strategic initiatives, ensuring the successful execution of clinical trials, and fostering relationships with key stakeholders.


As the Director of Clinical Operations, you will leverage your expertise to optimize clinical site performance, uphold the highest standards of quality, and lead a team of clinical professionals. Your focus will be on strategic oversight, operational excellence, and ensuring that all clinical activities align with organizational goals and regulatory requirements.


Key Responsibilities:

  • Strategic Leadership & Oversight: Provide direction and leadership to clinical operations teams, ensuring alignment with corporate objectives and the successful execution of clinical trials from start-up to close-out.
  • Quality Assurance: Ensure clinical trial activities adhere to regulatory requirements and Good Clinical Practice (GCP) guidelines, maintaining oversight on all aspects of site quality and study delivery.
  • Stakeholder Management: Develop and maintain strong relationships with internal teams, clinical site staff, and external partners to optimize study execution and address any challenges that may arise.
  • Operational Excellence: Manage and oversee the development, implementation, and maintenance of operational plans to enhance site performance and ensure timely delivery of clinical projects.
  • Team Development: Mentor and guide clinical research teams, fostering a collaborative and high-performance culture while ensuring professional development and compliance with best practices.
  • Risk Management: Identify potential risks and develop mitigation strategies to ensure seamless study execution and adherence to timelines.


Qualifications:

  • Experience: Minimum of 8-10 years of experience in clinical operations, with a proven track record of leadership within a Clinical Research Organization (CRO) or biopharmaceutical setting.
  • Expertise: In-depth knowledge of clinical trial management, ICH-GCP guidelines, and regulatory requirements, with the ability to evaluate medical data and oversee compliance.
  • Leadership: Demonstrated experience leading and managing clinical teams, with strong strategic thinking and problem-solving capabilities.
  • Communication Skills: Excellent interpersonal, verbal, and written communication skills, with the ability to influence and collaborate effectively across all levels of the organization.


Please reach out if this is anything of interest to you



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