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- Tasks: Lead and manage clinical trials, ensuring patient safety and regulatory compliance.
- Company: Join a top-tier clinical research organisation dedicated to innovative medical treatments.
- Benefits: Enjoy competitive benefits, including health insurance, paid time off, and a retirement plan.
- Why this job: Make a real impact in healthcare while working in a supportive, team-oriented environment.
- Qualifications: M.D. or D.O. with an active medical license; experience in clinical trials preferred.
- Other info: This role is urgent, so apply quickly to seize this exciting opportunity!
The predicted salary is between 48000 - 72000 £ per year.
A well-established and fully integrated clinical research organization is seeking a Principal Investigator (PI) to join its team in East London. This organization is committed to advancing innovative medical treatments through excellence in patient care and the generation of high-quality clinical data.
The company supports its employees with competitive benefits, professional development opportunities, and a strong emphasis on teamwork, integrity, and patient-centered care. Benefits include medical, dental, and vision insurance, paid time off and holidays, a 401(k) retirement plan with company match, and an annual incentive program.
Position Summary
The Principal Investigator is responsible for the medical oversight, execution, and management of clinical trials conducted at the site. This role requires strong collaboration with internal teams and external sponsors, while ensuring adherence to regulatory requirements and ethical standards in research.
Key Responsibilities
- Provide overall medical direction and oversight for clinical trials
- Review and approve study protocols and ensure alignment with good clinical practice (GCP)
- Protect the safety, rights, and confidentiality of all study participants
- Evaluate medical history, perform physical examinations, and conduct study-related assessments
- Interpret clinical data, lab results, ECGs, and diagnostic reports
- Report Serious Adverse Events (SAEs) in compliance with regulatory timelines
- Oversee administration of investigational products and adherence to study protocols
- Maintain thorough and timely documentation of all study-related activities
- Ensure compliance with IRB/ethics committee requirements and regulatory guidelines
Required Skills & Competencies
- In-depth understanding of ICH GCP, FDA regulations, and clinical research ethics
- Strong clinical judgment and attention to detail
- Effective and flexible communication skills
Qualifications
- M.D. or D.O. with a valid and active medical license (must be valid in the state where the research is conducted)
- Board certified or board eligible in a relevant specialty
- Certification in Good Clinical Practice (GCP)
- Prior experience in clinical trials or research (preferred)
Principal Investigator - Clinical Trials employer: Silver Birch Rec Ltd T/A Etech Partners
Contact Detail:
Silver Birch Rec Ltd T/A Etech Partners Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Investigator - Clinical Trials
✨Tip Number 1
Network with professionals in the clinical research field. Attend industry conferences or local meetups to connect with other Principal Investigators and learn about potential job openings. Building relationships can often lead to opportunities that aren't advertised.
✨Tip Number 2
Stay updated on the latest developments in clinical trials and regulations. Subscribe to relevant journals or follow key organisations on social media. This knowledge will not only enhance your expertise but also demonstrate your commitment to the field during interviews.
✨Tip Number 3
Consider reaching out directly to the hiring managers or team members at the organisation. A brief, professional message expressing your interest in the Principal Investigator role can make a memorable impression and show your proactive approach.
✨Tip Number 4
Prepare for potential interviews by reviewing common questions related to clinical trial management and ethical considerations. Practising your responses will help you articulate your experience and qualifications effectively when the time comes.
We think you need these skills to ace Principal Investigator - Clinical Trials
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Principal Investigator position. Familiarise yourself with clinical trial processes, regulatory guidelines, and the specific competencies needed for this role.
Tailor Your CV: Craft your CV to highlight relevant experience in clinical trials and research. Emphasise your medical qualifications, certifications, and any previous roles that demonstrate your ability to manage clinical studies effectively.
Write a Compelling Cover Letter: Your cover letter should reflect your passion for clinical research and patient care. Discuss your understanding of GCP and FDA regulations, and how your skills align with the company's commitment to high-quality clinical data and patient safety.
Proofread and Format: Ensure your application documents are free from errors and professionally formatted. A well-organised and polished application reflects your attention to detail, which is crucial for a Principal Investigator.
How to prepare for a job interview at Silver Birch Rec Ltd T/A Etech Partners
✨Know Your Clinical Research
Make sure you have a solid understanding of ICH GCP, FDA regulations, and clinical research ethics. Brush up on recent developments in clinical trials to demonstrate your expertise and commitment to the field.
✨Prepare for Scenario Questions
Expect questions that assess your clinical judgment and decision-making skills. Prepare examples from your past experiences where you successfully managed patient safety or navigated complex trial protocols.
✨Showcase Your Communication Skills
Effective communication is key in this role. Be ready to discuss how you've collaborated with internal teams and external sponsors in previous positions, highlighting your ability to convey complex information clearly.
✨Emphasise Patient-Centred Care
Since the organisation values patient care, be prepared to discuss how you prioritise the safety, rights, and confidentiality of study participants. Share specific instances where you advocated for patients during trials.
