Research Coordinator

1 day ago


Belfast, United Kingdom Queens University Full time
Job Overview
  We are seeking a skilled Clinical Trials Specialist to join our team at Queen's University. This is an exciting opportunity for individuals with a strong background in healthcare and clinical trials research.

About the Role
  As a Clinical Trials Specialist, you will play a key role in assisting our team to catalyse our clinical trial growth and drive high-quality research and excellence in clinical trial delivery. The post will initially be based in the Northern Ireland Clinical Research Facility (NICRF) but will be relocated within iREACH Health building on Belfast City Hospital site. iREACH Health is an innovative project that brings together academia, industry, the NHS, and public sector/government stakeholders to drive UK science and innovation and focuses on modernising our research infrastructure. The outcome of this collaboration will drive continuous improvement in patient care and outcomes through innovation by integrating the activities of clinicians, life scientists, and data scientists with industry partners to identify and develop new diagnostic tests, treatments, and health-related technologies. About the person: The successful candidate must have academic or vocational qualifications and relevant work experience including experience of processing biological samples. A competitive salary of £25,000 - £35,000 per annum, depending on experience, as well as a comprehensive benefits package including holiday entitlement, pension schemes, and development opportunities, makes this an attractive offer for candidates looking to advance their careers. Beyond the salary and benefits, we offer flexible working options, work-life balance initiatives, and support for physical and mental health. We subscribe to Equality Charter Marks such as the Diversity Charter Mark NI and Athena Swan and have established staff networks such as iRise (Black, Asian, Minority Ethnic and International Staff Network) and PRISM (LGBTQ+) which help us progress further information on our commitment to Equality, Diversity, and Inclusion, please visit our website.

Key Responsibilities
  
  1. Assist in the coordination and management of clinical trials, ensuring compliance with regulatory requirements and organisational policies.
  2. Work closely with researchers, clinicians, and industry partners to identify and develop new diagnostic tests, treatments, and health-related technologies.
  3. Process biological samples and maintain accurate records of sample handling and storage.
By joining our team, you will contribute to advancing medical knowledge and improving patient care. If you have the skills and passion to make a difference, we encourage you to apply for this challenging and rewarding role.

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