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For Companies At a Glance
- 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. Demonstrating your knowledge during interviews can set you apart from other candidates.
✨Tip Number 3
Consider reaching out directly to the hiring manager or team members at the organisation. A brief, professional email expressing your interest and asking insightful questions can make a memorable impression and show your enthusiasm for the role.
✨Tip Number 4
Prepare for the interview by reviewing common questions for Principal Investigator roles. Focus on your experience with clinical trials, patient safety, and regulatory compliance. Practising your responses will help you convey confidence and expertise during the interview.
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, medical oversight, and any certifications such as Good Clinical Practice (GCP). Emphasise your qualifications, including your medical degree and any board certifications.
Write a Compelling Cover Letter: Your cover letter should reflect your passion for clinical research and patient care. Discuss your previous experiences that align with the job description, and explain why you are a great fit for the team and the organisation's mission.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application demonstrates attention to detail, which is crucial for a Principal Investigator role.
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, objectives, and methodologies of the studies. This will not only show your expertise but also your commitment to patient safety and ethical standards.
✨Demonstrate Strong Communication Skills
As a Principal Investigator, you'll need to collaborate with various teams and sponsors. Practice articulating your thoughts clearly and concisely. Be prepared to discuss how you would handle communication challenges in a clinical setting.
✨Highlight Your Regulatory Knowledge
Be ready to discuss your understanding of ICH GCP, FDA regulations, and clinical research ethics. Prepare examples from your past experiences where you ensured compliance with these guidelines, as this is crucial for the role.
✨Showcase Your Leadership Experience
Since the role involves medical oversight and management of trials, be prepared to share instances where you've led a team or project. Highlight your ability to make critical decisions and maintain high standards in clinical practice.
