NIHR Dorset PC CRDC Data Manger

Develop effective working relationships with the

site Principal Investigators, Sponsor team and other study staff to ensure

appropriate support is in place to conduct research safely, efficiently and

effectively.

Ensure

a consistent approach to local study documentation taking account of

regulations and external requirements e.g. Trial Master Files.

Co-ordinate data

collection: ensure timely submission of accrual data; review data for

completeness and accuracy where appropriate, liaising closely with the study

management team.

Monitor

trial progress to ensure compliance with and adherence to the project plan and

to identify, evaluate and help rectify problems alongside the Project Manager.

Co-ordinate the

design, printing and distribution of trial documentation, and ensure all

paperwork is of the appropriate standard.

Provide

a high standard of data entry within databases and study management systems,

this includes working within a variety of web-based platforms.

Create

and maintain the study Investigator Site files and oversight of site files,

ensuring these are kept tidy and current by appropriate filing of

documentation.

Support the coordination and preparation of documentation required for

regulatory monitoring and auditing.

Maintain

awareness of regulatory requirements, i.e. NHS Research Ethics Committee, UK

Policy Framework for Health and Social Care Research (2017), ICH-GCP, GDPR, and

advise others accordingly.

Take

responsibility for the necessary study applications as appropriate and assisting, advising participating investigators with local requirements.

Support

feasibility and risk assessment of assigned studies along with the Clinical

Trials Manager whilst maintaining comprehensive knowledge of resources available

to assist researchers in the development and delivery of high-quality clinical

research.

Ensure a

consistent approach to local study documentation taking account of regulations

and external requirements e.g. Investigators Site Files (ISFs)

Promote and advise on the principles of Good Clinical Practice (GCP) and

Good Research Practice within The Adam Practice Research team & DPCCRG.

Build

and maintain a productive working relationship with colleagues across the

organisations involved in study delivery and clinical networks

Communicate

with participating sites across the network to ensure current knowledge on

study recruitment and performance evaluation against targets.

Support research

study management and high-quality study delivery.

The Adam Practice is a partnership located across 5 surgeries in Poole, Dorset. This is an exciting opportunity to join our growing primary care team in a forward- thinking, innovative, general practice, which has a current CQC rating ofOutstanding in Care.

Here are some of our many benefits we offer;

Access to NHS Pension Scheme and NHS discounts, 5 weeks annual leave (inclusive of bank/public holidays that fall in the holiday year). Entitlement is pro-rata for part-time employees.

Auto enrolment in NHS Pension Scheme.

Cycle to work scheme.

Experience

Qualifications

Qualities and Attributes