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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: 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 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)
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 trends and regulations in clinical trials. Familiarise yourself with ICH GCP and FDA guidelines, as well as any recent changes in the field. This knowledge will not only enhance your expertise but also demonstrate your commitment to the role during interviews.
✨Tip Number 3
Prepare for interviews by reviewing common questions specific to Principal Investigator roles. Be ready to discuss your previous experiences in clinical trials, how you handle ethical dilemmas, and your approach to patient safety. Practising your responses can help you feel more confident.
✨Tip Number 4
Showcase your leadership skills and ability to collaborate effectively. As a Principal Investigator, you'll need to work closely with various teams. Highlight any past experiences where you've successfully led a team or managed a project, as this will be crucial in your application.
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 medical qualifications and any previous roles that demonstrate your ability to manage clinical research effectively.
Write a Compelling Cover Letter: In your cover letter, express your passion for clinical research and patient care. Mention specific experiences that align with the job description, such as your understanding of ICH GCP and FDA regulations, and how you can contribute to the organisation's goals.
Proofread and Format: Ensure your application documents are free from errors and formatted professionally. Use clear headings, bullet points for easy reading, and maintain a consistent style throughout your CV and cover letter to make a strong impression.
How to prepare for a job interview at Silver Birch Rec Ltd T/A Etech Partners
✨Know Your Clinical Research Fundamentals
Make sure you have a solid understanding of ICH GCP, FDA regulations, and clinical research ethics. Brush up on these topics before the interview, as they are crucial for the role of Principal Investigator.
✨Demonstrate Strong Communication Skills
Effective communication is key in this role. Be prepared to discuss how you've collaborated with internal teams and external sponsors in past projects. Use specific examples to showcase your ability to convey complex information clearly.
✨Prepare for Scenario-Based Questions
Expect questions that assess your clinical judgment and decision-making skills. Think of scenarios where you had to evaluate medical history or report Serious Adverse Events, and be ready to explain your thought process.
✨Showcase Your Commitment to Patient Safety
As a Principal Investigator, protecting the safety and rights of study participants is paramount. Be prepared to discuss how you ensure compliance with ethical standards and regulatory guidelines in your previous roles.
