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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: 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, 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, seminars, or local meetups to connect with other Principal Investigators and learn about potential job openings.
✨Tip Number 2
Stay updated on the latest trends and regulations in clinical trials. Familiarise yourself with ICH GCP and FDA guidelines, as this knowledge will be crucial during interviews and discussions with potential employers.
✨Tip Number 3
Consider reaching out directly to the hiring manager or team members at the organisation. A brief, professional message expressing your interest can help you stand out and demonstrate your enthusiasm for the role.
✨Tip Number 4
Prepare for interviews by practising common questions related to clinical trial management and ethical considerations. Being able to articulate your experience and approach to patient care will showcase your suitability for the position.
We think you need these skills to ace Principal Investigator - Clinical Trials
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trials and research. Emphasise your medical qualifications, certifications, and any previous roles that demonstrate your ability to oversee clinical studies.
Craft a Strong Cover Letter: Write a compelling cover letter that outlines your passion for clinical research and patient care. Mention specific experiences that align with the responsibilities of a Principal Investigator and how you can contribute to the organisation's goals.
Highlight Regulatory Knowledge: In your application, clearly demonstrate your understanding of ICH GCP, FDA regulations, and ethical standards in clinical research. This will show that you are well-prepared for the compliance aspects of the role.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects attention to detail, which is crucial in clinical research.
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've worked on. Be prepared to discuss specific protocols, your role in them, and how you ensured compliance with GCP and regulatory 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, and be ready to provide examples of how you've effectively communicated in past roles.
✨Highlight Your Ethical Standards
Ethics are crucial in clinical research. Be prepared to discuss how you've prioritised patient safety and confidentiality in your previous work, and how you ensure adherence to ethical guidelines in your research.
✨Prepare for Scenario-Based Questions
Expect questions that assess your clinical judgment and decision-making skills. Think of scenarios where you had to make tough calls regarding patient care or trial management, and be ready to explain your thought process.
