Clinical Research Coordinator

4 weeks ago

London, Greater London, United Kingdom University College London Hospitals NHS Foundation Trust Full time

Position Overview

The Clinical Research Coordinator is a key professional within a collaborative healthcare team, responsible for overseeing and managing a diverse portfolio of clinical research initiatives, including both local and global phase II and III trials focused on oncology and hematological disorders.

Key Responsibilities

Research Management

  • Oversees and executes both in-house and external clinical trials, ensuring compliance with regulatory standards.
  • Facilitates the submission of new research protocols for ethical and administrative review.
  • Maintains comprehensive trial documentation and site files.
  • Ensures that all necessary patient information and consent documentation are current and accessible.
  • Accountable for accurate data collection and documentation in accordance with established guidelines.
  • Utilizes critical thinking skills to assess and evaluate research proposals.
  • Contributes to the development and upkeep of relevant databases.
  • Collaborates effectively with multidisciplinary teams to enhance the execution of clinical research protocols.
  • Engages with principal investigators and research organizations to refine and implement research strategies.
  • Gains in-depth knowledge of investigational therapies and their underlying scientific rationale.
  • Ensures timely completion of trial documentation in line with regulatory requirements.

Clinical Responsibilities

  • Demonstrates independence while working collaboratively within a healthcare team to address patient and family needs throughout the healthcare process.
  • Coordinates patient care for those enrolled in clinical trials, including:
    • Identifying and evaluating potential trial participants.
    • Conducting necessary pre-study assessments.
    • Acting as a patient advocate and facilitating informed consent processes.
    • Documenting patient interactions and care in medical records.
    • Collecting and processing biological samples as per study protocols.
  • Maintains high standards of nursing care tailored to the specific needs of clinical trial participants.

Communication and Education

  • Disseminates research protocol information to healthcare professionals through various educational methods.
  • Serves as a primary contact for patients involved in clinical trials, providing comprehensive information about trial objectives and procedures.
  • Develops individualized care plans for trial participants.
  • Establishes and nurtures relationships with external healthcare providers.

Professional Development

  • Engages in ongoing professional education and training to stay current with advancements in oncology and clinical research.
  • Participates in the orientation and training of new staff members.
  • Contributes to educational initiatives within the organization.

Organizational Commitment

UCLH is dedicated to providing exceptional patient care and advancing medical research. The Clinical Research Coordinator plays a vital role in achieving these goals by ensuring the highest standards of clinical trial management and patient advocacy.

All staff members are expected to adhere to organizational policies and procedures, promoting a safe and respectful environment for patients and colleagues alike.

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