Lead Clinical Trials Coordinator

3 weeks ago

Cambridge, Cambridgeshire, United Kingdom Cambridge University Hospital NHS Foundation Trust Full time

Position Overview

As a Lead Clinical Trials Coordinator, you will take charge of a diverse portfolio of clinical studies, overseeing the entire trial setup process from inception to conclusion, ensuring efficiency and timeliness throughout.

You will play a crucial role within the clinical trials team, facilitating the prompt initiation of trials to ensure that innovative therapies are accessible to patients in need.

Key Responsibilities

You will independently manage applications to all pertinent regulatory and ethical bodies to secure approvals for clinical research protocols, including those developed internally.

  • Collaborate with study investigators and research personnel to guarantee adherence to local standard operating procedures (SOPs) and ensure that new research protocols are created and submitted as scheduled by the Principal Investigator.
  • Assume responsibility for a portfolio of trials, ensuring that all processes are meticulously followed, tracked, and verified to maintain compliance with regulatory standards.

About Cambridge University Hospitals

Cambridge University Hospitals NHS Foundation Trust encompasses two major hospitals, providing exceptional healthcare services. With a workforce exceeding 13,000 and over 1,100 beds, our Trust prioritizes delivering high-quality care centered around patients, staff, and partners. Our commitment to excellence is reflected in our outstanding ratings for patient care.

We are dedicated to fostering a diverse and inclusive environment where every individual can thrive. We value our differences and actively support an inclusive workplace that reflects the communities we serve.

Job Responsibilities

For a comprehensive overview of the key duties and responsibilities, please refer to the attached Applicant Information Pack.

Benefits

We provide numerous development opportunities and a variety of benefits, including on-site fitness facilities, shopping amenities, childcare services, and convenient access to transportation options.

Qualifications and Experience

Essential Qualifications

  • A degree or equivalent qualification in a relevant field such as Service/Business Administration or IT.

Essential Experience

  • Extensive knowledge and experience in the setup of cancer clinical trials.
  • Proven experience in data collection within a scientific or medical context.
  • Familiarity with clinical trials databases.
  • Strong organizational skills with the ability to prioritize and manage tasks effectively.
  • Experience working independently within established guidelines and under tight deadlines.
  • Ability to collaborate across multidisciplinary teams.
  • Experience liaising with external organizations.

Knowledge and Skills

Essential Knowledge

  • Comprehensive understanding of ethical and quality standards relevant to clinical trials.
  • GCP trained.
  • Proficient in Microsoft Office applications.
  • Awareness of confidentiality and data protection regulations.

Essential Skills

  • Strong teamwork capabilities.
  • Excellent communication skills across various mediums.
  • Willingness to learn and develop new skills.
  • Attention to detail and accuracy.
  • Adaptability to change.
  • Ability to work effectively under pressure.
  • Competence in managing confidential information.

Desirable Skills

  • Ability to analyze and interpret clinical data for research purposes.

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