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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 patient care and impactful research.
- 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 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, seminars, or local meetups to connect with other Principal Investigators and learn about potential job openings at organisations like ours.
✨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 not only enhance your expertise but also demonstrate your commitment to the role during interviews.
✨Tip Number 3
Consider reaching out directly to our recruitment team or hiring managers via LinkedIn. A personalised message expressing your interest in the Principal Investigator position can help you stand out from other candidates.
✨Tip Number 4
Prepare for potential interviews by practising common questions related to clinical trial management and ethical considerations. Being well-prepared will boost your confidence and help you articulate your experience effectively.
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 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 Inside Out
Make sure you have a solid understanding of ICH GCP, FDA regulations, and clinical research ethics. Be prepared to discuss how these guidelines influence your approach to clinical trials and patient safety.
✨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.
✨Showcase Your Medical Oversight Experience
Be ready to discuss your previous experience in providing medical direction for clinical trials. Highlight specific instances where you ensured compliance with study protocols and maintained participant safety.
✨Prepare for Ethical Dilemmas
Expect questions about how you would handle ethical challenges in clinical research. Think through scenarios where you had to protect participant rights and confidentiality, and be prepared to explain your decision-making process.
