We are seeking an experienced and skilled Principal Investigator to spearhead early-stage clinical trials, manage study protocols, and ensure ethical conduct and compliance at all stages.
This role offers tremendous scope for leadership and personal development. The successful candidate will have the opportunity to grow and nurture a clinical research team, as well as have significant involvement and influence with sponsors.
* Provide medical direction, oversee protocol compliance, and ensure participant safety throughout clinical trials.
* Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
* Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
* Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.
The ideal candidate will possess a medical degree (MD) and full current GMC registration. Strong experience in clinical research/clinical trials and proven leadership skills are also essential.
A strong knowledge of regulatory guidelines and excellent organisational, communication, and analytical skills are required for this position.
We pride ourselves on being an Equal Opportunities Employer and welcome applications from diverse candidates. If you are a motivated and experienced professional looking to take on a challenging role, please apply now.
Key Responsibilities:
* Medical Direction
* Protocol Compliance
* Clinical Data Evaluation
* Scientific Feasibility
* Regulatory Requirements
Requirements:
* Medical Degree (MD)
* Full Current GMC Registration
* Strong Background in Clinical Research/Clinical Trials
* Proven Leadership Skills
* Strong Knowledge of Regulatory Guidelines