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Clinical Research Specialist
2 months ago
Position Overview
Fixed-term contract opportunity
Are you driven by a commitment to advancing medical knowledge? If you are a qualified Registered Nurse with a strong interest in clinical research, this role may be a perfect fit for you. The Research and Development department is seeking Clinical Research Specialists to engage in a variety of specialized research initiatives.
If you thrive in a dynamic environment and find fulfillment in contributing to impactful research, we encourage you to explore this opportunity. You are welcome to reach out to the Lead Research Nurse for more information about this position and to arrange a visit to our team.
We are looking for a dedicated and proactive nurse to join our research team. The successful candidate will oversee the coordination and management of clinical trials, working collaboratively with essential personnel across the organization to ensure comprehensive care and support for participants involved in research studies.
Key Responsibilities
The selected individual will manage multiple trials, with duties including participant recruitment and execution of trial-specific procedures. Strong communication skills are essential, as you will collaborate within a multidisciplinary team, alongside meticulous record-keeping and organizational abilities, while adhering to data protection regulations.
The role involves close collaboration with healthcare teams associated with the multidisciplinary unit. Key responsibilities include:
- Identifying patients who qualify for clinical trials.
- Providing information and support to patients participating in clinical trials.
- Facilitating the informed consent process.
- Coordinating patient treatment, assessments, follow-ups, and data collection in accordance with clinical trial protocols.
The post-holder will be expected to work independently while also collaborating with other research team members to deliver a comprehensive clinical trial service.
About Our Organization
The Bedfordshire Hospitals NHS Foundation Trust serves a diverse population, providing essential hospital services across two busy sites. Our organization is committed to delivering high-quality patient care and fostering the health and well-being of our staff. As one of the largest NHS Trusts in the region, we offer extensive training and development opportunities to support your career growth.
Our Core Values
We prioritize recruiting individuals who embody our Trust's core values, focusing on inclusivity and diversity. We strive to create a culture that values differences and promotes equality.
Please be aware that vacancies may close before the advertised date if a sufficient number of applications are received.
All new hires will undergo a probationary period during their initial months in the role. Travel between hospital sites may be necessary.
We encourage you to review all attached documents to familiarize yourself with the job requirements.
Responsibilities Overview
Clinical Duties
- Identify eligible patients for clinical trials and maintain comprehensive knowledge of trial protocols.
- Provide verbal and written information to support patients and caregivers throughout their involvement in clinical trials.
- Ensure informed consent is obtained from all study participants prior to any study-related procedures.
- Carry out planned care as dictated by the clinical trial protocol.
- Responsible for setting up, recruiting, and following up with patients in studies, including randomized clinical trials.
- Act as an advocate for patients, ensuring they make informed decisions regarding their participation in clinical trials.
Administrative Duties
- Assist in providing background information for potential clinical trials to secure approvals from relevant committees.
- Collaborate with research clinicians, nurses, and pharmacists within the region.
- Ensure all personnel involved in clinical trials are informed of any protocol changes.
Research and Development Responsibilities
- Adhere to regulations outlined in ICH Good Clinical Practice and EU Directives.
- Participate in the informed consent process, safety reporting, and protocol compliance.
- Maintain awareness of current treatments and national clinical trials available to patients.
Education and Training Responsibilities
- Assist in educating healthcare professionals to enable them to care for clinical trial patients.
- Maintain an up-to-date knowledge of research-related topics, particularly in clinical trials.
- Act as a mentor and role model for the nursing team.
