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Clinical Research Coordinator

3 months ago

London, Greater London, United Kingdom PROSPECTUS-4 Full time £21 - £25

Position Overview: Our client, PROSPECTUS-4, is in search of a proactive and skilled individual to take on the role of Clinical Research Coordinator. This position involves a commitment of 35 hours per week and offers a flexible working arrangement, allowing for a combination of on-site and remote work.

Key Responsibilities:

  • Oversee the comprehensive setup and management of clinical trials and feasibility assessments.
  • Serve as the primary point of contact among various stakeholders involved in the research process.
  • Track the progress of clinical trials, ensuring compliance with the project timeline, while identifying and addressing any issues that may arise at different trial locations.
  • Conduct site visits as necessary to perform monitoring tasks, verify source data, and ensure compliance with relevant protocols and regulations.
  • Handle financial documentation, including invoices, credit notes, and expense claims for participating sites, ensuring all records are current.
  • Provide regular and on-demand information to trial sites, including reports, updates, and guidance.
  • Establish and implement procedures to ensure compliance with protocols and administrative requirements, while training staff on relevant processes.
  • Stay informed on subject-related and professional developments by attending meetings, conferences, and training sessions, and applying this knowledge to enhance work practices.
  • Prepare progress reports for the Trial Management Group, Steering Committees, and other relevant stakeholders.
  • Maintain trial documentation, overseeing the management of master and site files.
  • Ensure accurate record-keeping, maintaining confidentiality and security of all stored data in accordance with data protection regulations.

Qualifications:

  • Proven experience in a similar capacity, ideally within an academic or research institution.
  • Strong background in managing or coordinating clinical research projects, particularly multi-centre trials.
  • Experience working with patients and research participants.
  • Familiarity with study development and setup, including the necessary procedures for obtaining study approval.
  • Understanding of research and development processes and sponsor organizations.
  • Knowledge of good clinical practices and data protection guidelines.
  • Exceptional communication and organizational skills, with a strong attention to detail.
  • Demonstrated commitment to advancing knowledge and understanding of diversity issues.
  • Proficient in various IT systems.
  • Strong interpersonal skills, facilitating effective interactions with both internal and external stakeholders.
  • Analytical mindset with the ability to solve problems and make informed decisions quickly.

Application Process: Interested candidates are encouraged to submit their CV in Word format for consideration.

Commitment to Diversity: PROSPECTUS-4 is dedicated to fostering inclusive and diverse workplaces and welcomes applications from all segments of the community.