Study Coordinator

Join to apply for the Study Coordinator role at St Pancras Clinical Research

Due to continued growth and expansion, St Pancras Clinical Research is looking to recruit an experienced Study Coordinator to join our dynamic team at our Eastbourne site.

Established in 2016, St Pancras Clinical Research is a London-based Site Management Organisation with three sites in the UK - London, Chester and Eastbourne. We conduct Phase II and III clinical trials with new medicines, for patients with various chronic diseases. Our experience includes chronic pain and memory disorders resulting from inflammatory, neurological and neurodegenerative conditions, as well as diabetes and dermatology.

In addition, our clinical and scientific specialists offer wide-ranging and practical expert advice to sponsors on their drug development programmes, based upon substantial experience in the public, private, academic and commercial pharma fields.

The Study Coordinator will be responsible at St Pancras Clinical Research Ltd (SPCR) for the day-to-day coordination and administration of all aspects of our ongoing clinical trials, as regulated by the research protocols (approved by the Research Ethics Committees of the UK Health Regulatory Authority (HRA) & the Medicines and Healthcare products Regulatory Agency (MHRA), Good Clinical Practice (GCP) guidelines and supporting legislation, while abiding by SPCR’s Policies and Standard Operating Practices.

The Study Coordinator will work within the Clinical Team to ensure the successful delivery of research at SPCR.

• Managing all aspects of your allocated clinical trials, including patient visit management, data management and pharmacy activities.
• Working alongside the clinical team to deliver timely, efficient and high-quality clinical trial data.
• Ensuring the highest standard of care for our patients. Performing all tasks relating to the clinical trials in strict adherence to the trial protocols.
• Performing administrative tasks of any kind relating to clinical trials.
• Laboratory work.
• Assisting with patient recruitment.
• Salary: starting at £30,000 p.a.; dependent upon experience.

• 1 year minimum clinical research coordinator experience in CTIMPs.
• A strong understanding and practical experience of ICH Good Clinical Practice (GCP).
• Patient-centric approach to clinical and research practice. Flexible and can do attitude.
• IT literate - experience of Microsoft Office applications; electronic databases; and data entry systems.
• Qualities St Pancras Clinical Research are looking for: team player; diligent and high level of attention to detail; willing to work in high pressure environment with strict targets and deadlines; and able to manage multiple projects with efficiency and produce high quality work.

This vacancy may close before the current listed closing date. You are advised not to delay submitting your completed application. Any applicants submitted after the deadline will not be considered.

Please note due to the high number of applicants we will only be able to provide feedback for those invited to the interview stage. If you do not hear back from us after 3 weeks of your application being submitted, then unfortunately your application has been unsuccessful.

• Mid-Senior level

• Full-time

• Research, Analyst, and Information Technology

• Research Services