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For Companies At a Glance
- Tasks: Lead and manage clinical trials, ensuring patient safety and data integrity.
- 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: Be part of a collaborative team focused on impactful medical research and patient care.
- Qualifications: M.D. or D.O. with an active medical license; experience in clinical trials preferred.
- Other info: This role is urgent; apply quickly to seize this exciting opportunity!
The predicted salary is between 43200 - 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)
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 that may not be advertised.
✨Tip Number 2
Stay updated on the latest trends and regulations in clinical trials. Familiarise yourself with ICH GCP and FDA guidelines, as demonstrating your knowledge during interviews can set you apart from other candidates.
✨Tip Number 3
Consider reaching out to current employees at the organisation for informational interviews. This can provide you with insights into the company culture and expectations, which can be beneficial when preparing for your interview.
✨Tip Number 4
Prepare specific examples of your past experiences in clinical trials. Be ready to discuss how you've managed trials, ensured compliance, and handled adverse events, as these are crucial aspects of the Principal Investigator role.
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 oversee 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 formatted professionally. A well-organised CV and cover letter can make a strong impression, so take the time to review and refine your submission before sending it off.
How to prepare for a job interview at Silver Birch Rec Ltd T/A Etech Partners
✨Know Your Clinical Trials Inside Out
Make sure you have a solid understanding of the clinical trials you will be overseeing. Familiarise yourself with the protocols, regulatory requirements, and ethical standards. This knowledge will not only help you answer questions confidently but also demonstrate your commitment to patient safety and quality data.
✨Showcase Your Leadership Skills
As a Principal Investigator, you'll need to lead teams effectively. Be prepared to discuss your previous experiences in managing clinical trials and how you foster collaboration among team members. Highlight any specific instances where your leadership made a significant impact on trial outcomes.
✨Prepare for Ethical Dilemmas
Expect questions about how you would handle ethical challenges in clinical research. Think about scenarios involving patient safety, informed consent, or adverse events. Articulating your thought process and decision-making skills in these situations will show your integrity and commitment to ethical standards.
✨Demonstrate Effective Communication
Effective communication is key in this role, especially when liaising with sponsors and internal teams. Prepare examples of how you've successfully communicated complex information in the past. This could include presenting data, writing reports, or discussing trial results with stakeholders.
