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An established industry player in healthcare is seeking a dedicated individual to assist in managing research projects. This role involves supporting the setup and conduct of clinical trials, ensuring compliance with health research standards, and maintaining accurate documentation. The ideal candidate will possess strong communication and organisational skills, along with a foundational understanding of health research in the UK. Join a team that values your contributions and offers a dynamic environment where you can grow and develop your skills while making a meaningful impact in the healthcare sector.
Will assist in the management of research projects providing the necessary support so that studies can be set up and conducted safely, efficiently according to the required standards & targets.
Assist in the delivery of recruitment targets in line with the contractual agreements, agreed timelines.
Open and manage allocated projects, set timescales and resolve problems. This includes management of the set-up process.
Take responsibility for all areas of practice relating to the conduct of clinical trials and research studies.
Maintain accurate records of portfolio activities.
Under supervision, report, address, help to resolve any breaches and protocol deviations. Report Adverse Events (AEs) using appropriate procedures, including the expedited reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs).
Prepare/assist with preparation of patient documentation for research-related treatment clinics, complete accurate records of patient care, maintain source data and Case Report Forms and all other trial documents in a manner conducive to audit.