Contract Type:
Contract
Hours:
Full time
Disability Confident:
No
Closing Date:
11/06/2026
About this job
Assimilate study protocols and co-ordinate the wider research team's efforts by scheduling and delegation of tasks.
Conduct searches on the EMIS platform to identify potential study participants.
Contribute to the delivery of individual studies, including acting as a contact point for participants, assisting with data collection, and completion of other tasks as necessary, under the direction of the Principal Investigator, sub-investigator or nurse lead for that study.
Ensure research equipment is maintained and calibrated in accordance with manufacturer's instructions, and track capacity of storage requirements.
Organise wider logistical elements of study delivery including the monitoring, restocking and disposal of consumables.
Create and maintain data-bases and trackers to ensure efficient scheduling and running of patient visits, and administrative tasks including expense claims.
Support the wider team to organise and deliver site visits including the preparation of consumables, the processing, storage and onward shipping of study samples.
Support research team members to maintain sponsor IT platform access as needed.
Track and manage financial claims with the NIHR's South West Central Regional Research Delivery Network, and commercial sponsors.
Act as administrator for the research team's activities including calendar management and scheduling of meetings, participant visits, and sponsor visits.
Ensure documentation is accurate, organised and auditable at all times, and archived in accordance with regulations.
Contribute to study documentation and notes to files as needed.
Act as the central point of contact for internal and external queries.
Respond promptly and effectively to queries from the wider research team, study sponsors, NIHR contacts, and regulatory bodies.
Facilitate sponsor site visits, ensuring appropriate response to data queries, collation of adverse event reports, and preparation for data locks.
Develop and maintain the public facing profile of our organisation's research activities including maintaining an up to date and accurate profile of the studies we collaborate with and opportunities for participation.
Work with our PCN's Community Engagement Lead to identify opportunities to widen research participation in historically less well represented demographic groups.
Compile regular reports on the team's research activity for presentation to the practice's partners and management team.
Contribute to the oversight of the team's compliance with regulatory responsibilities and specific protocol requirements.
Contribute to security in data handling such that it meets sponsor and regulatory requirements throughout the study lifecyle.
Assist the wider team with equipment monitoring activities including temperature checks.
Contribute to the development of policies, protocols and standard operating procedures that ensure compliant, standardised activity across the research team.
Oversee maintenance of up to date training logs, delegation logs and staff records including GCP training and research CVs, for all members of the research team across all research activities.
Participate in ongoing training and development to keep an up to date knowledge of regulatory responsibilities and best practice.
#J-18808-Ljbffr