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Clinical Sub-Investigator

Pharmaceutical

West Midlands £55k – £60k
permanent Job Ref: 6345

Description

A leading provider of clinical services is looking for a Sub-Investigator to join its growing team. You will be responsible for the conduct of the trial including the wellbeing of your subjects enrolled in the study and you may delegate specific duties to trained members of your team. You must be GMC registered and have significant experience working within clinical trials and with MHRA regulations to apply for this role.

Responsibilities:

  1. Working under the direct supervision of the Principal Investigator
  2. Performing the studies in accordance with ICH GCP (R2)
  3. Ensuring that adequate time and appropriate resources are available to perform the study as described in this protocol
  4. Ensuring that all persons assisting with the trial are adequately qualified persons to whom duties have been delegated
  5. Signing an Investigator Agreement to confirm acceptance and willingness to comply with the study protocol
  6. Maintaining adequate records of each subject’s participation
  7. Managing the clinical trial team – supervising, mentoring, training, risk management, etc.
  8. To undertake specific administrative duties as required including appropriate record-keeping
  9. To perform other duties of a similar nature appropriate to your position which may be required from time to time by the line manager
  10. Plan and prioritise own workload
  11. Work within Company operational and professional guidelines

Essential:

  • A medical doctor with 4 years of clinical experience (post-graduation)
  • Must have completed foundation and core medical competencies
  • GMC Registered
  • Significant experience within Clinical Trials
  • Experience with MHRA regulations

Desirable:

  • Postgraduate membership exams (like MRCP) would be highly favourable

This is a great opportunity to join one of the foremost providers of clinical trials in the world. 

Salary £55k - £60k

Job Ref: 6345