Principal Investigator

Although established in 2016, St Pancras Clinical Research has been highly successful in the trials undertaken thus far, achieving various milestones including a recent "Site Award" for its continued commitment to the development of medicines.

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.

Job Description:

• Taking on role of Principal Investigator on multiple Phase II and III clinical trials.
• Working with our Study Coordinators to deliver timely, efficient and high-quality clinical trial data.
• Conducting patient visits in strict adherence to study protocols.
• Performing duties of a clinical investigator according to the International Conference on Harmonisation (ICH) Good Clinical Practice (GCP), and ensuring the highest standard of care for our patients.
• Performing the following clinical procedures (non-exhaustive) as part of the conducting of clinical trials: completing Source Documents and Case Report Forms; assisting with the dosing of study medication; ensuring patient Informed Consent is obtained in line with study protocols; assessing and analysing clinical data such as BP, ECG's, laboratory tests, and adverse events according to study protocols; and performing pre-study medical histories and medical examinations as per SPCR’s SOPs.
• Providing medical cover for trial patients outside of working hours, as arranged in advance.
• Location: Chester research clinic.

Requirements:

• GMC registered with a licence to practice.
• Multiple years of clinical research experience including strong understanding of ICH Good Clinical Practice (GCP).
• Performed Principal Investigator role for CTIMP trials for minimum two years in the UK (NHS or private experience is acceptable).
• Patient-centric approach to clinical and research practice.
• Flexible attitude regarding work assignments and placements.
• Ability to perform CSF Sampling (LPs) is desirable.
• 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; able to work in high pressure environment; able to manage multiple projects with efficiency and produce high quality work.
• Ability to commute to the clinic in Chester.

Benefits:

• Company events
• Company pension

Schedule:

• Monday to Friday

Ability to commute/relocate:

• Chester: reliably commute or plan to relocate before starting work (required)

Education:

• Bachelor's (required)

Experience:

• Principal Investigator: 2 years (preferred)

Language:

• English (required)

Licence/Certification:

• GMC (required)

Work authorisation:

• United Kingdom (required)

Work Location: In person