Clinical Research Specialist

3 weeks ago

Torquay, Torbay, United Kingdom Torbay and South Devon NHS Foundation Trust Full time

Position Overview

An exciting opportunity has emerged for a Band 5 Clinical Research Specialist to join our dedicated Research Team.

The Clinical Research Specialist plays a crucial role within the clinical research team, ensuring the safe execution of research in compliance with the Research Governance Framework and Good Clinical Practice guidelines. This position is vital in safeguarding the rights, safety, and well-being of trial participants.

You will collaborate with the research team to strategize, execute, organize, and oversee multiple concurrent research initiatives. Establishing connections with Multidisciplinary Teams across the organization and other relevant local and national entities will be essential. You will coordinate and manage the pertinent study portfolio while achieving recruitment targets aligned with performance and monitoring objectives.

Additionally, you will be responsible for the implementation and oversight of clinical requirements associated with research, ensuring optimal execution of clinical trials. You will guarantee that all research procedures adhere to study protocols and will be accountable for the recruitment, data collection, and care of research participants, with a strong emphasis on delivering a quality experience.

Main Responsibilities

  • The research portfolio encompasses both randomized controlled trials and observational studies across various specialties. Our portfolio has expanded significantly in recent years, enabling us to provide our local patient population with access to cutting-edge clinical trials.
  • The successful candidate will need to be organized, motivated, and capable of prioritizing their workload. Responsibilities will include data collection and, under supervision, supporting the team with participant recruitment for trials. A key aspect of this role will involve liaising with all members of the multidisciplinary team, necessitating excellent interpersonal and communication skills.

This role presents an excellent opportunity for individuals looking to embark on a career in clinical research. Comprehensive training will be provided for research-specific procedures.

About Us

The clinical research delivery team recruits participants from across the organization into both commercial and non-commercial clinical trials and research studies. We support research across a variety of clinical specialties and departments.

Our team offers clinical research expertise from study setup with clinical services through to informed consent, trial treatments, interventions, and study follow-up. We utilize various clinical database systems to ensure high-quality clinical data collection.

We uphold the safe conduct of research in accordance with the Research Governance Framework and Good Clinical Practice guidelines, providing assurance that the rights, safety, and well-being of trial participants are protected.

Qualifications & Training

Essential

  • Relevant Healthcare Degree
  • Registered Nurse/AHP Practitioner

Desirable

  • Research training (GCP, degree module, or informed consent)

Knowledge and Experience

Essential

  • Demonstrable computer literacy, including ECDL qualification or similar ability, Outlook email and calendars, Microsoft Office proficiency, and basic Excel skills.
  • Understanding of the significance of research and the application of validated results to enhance practice.
  • Familiarity with data collection and entry for clinical trials.
  • Excellent communication skills.
  • Evidence of continued professional development.
  • Strong organizational skills with the ability to meet tight deadlines.
  • Ability to work independently and collaboratively within a team.
  • Flexibility and adaptability.
  • Commitment to openness, honesty, and integrity in performing the role.
  • Willingness to work across various sites, including community settings if required.
  • Ability to convey complex information to patients, caregivers, and team members.

Desirable

  • Venepuncture/Cannulation skills.
  • ECG Competency.
  • Knowledge of Research Governance Framework and GCP Guidelines.
  • Post-graduate qualification in teaching or equivalent.
  • Experience in Clinical Trials.
  • Familiarity with research methodologies and governance.
  • Proficiency in using established databases for data entry.
  • Proven track record of meeting targets.
  • Strong listening and counseling skills.
  • Ability to maintain focus for extended periods during data collection and trial protocol adherence.

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