Principal Investigator - Clinical Trials

Principal Investigator - Clinical Trials

Basildon Full-Time 54000 - 84000 £ / year (est.) No home office possible
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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 54000 - 84000 £ 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)
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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. Subscribe to relevant journals or online platforms that discuss advancements in clinical research. This knowledge will not only enhance your expertise but also demonstrate your commitment to the field during interviews.

✨Tip Number 3

Consider reaching out directly to the hiring managers or team members at the organisation. A brief, professional message expressing your interest in the Principal Investigator role can make a memorable impression and may even lead to an informal chat about the position.

✨Tip Number 4

Prepare for potential interviews by reviewing common questions specific to Principal Investigator roles. Focus on scenarios involving ethical dilemmas, patient safety, and regulatory compliance, as these are crucial aspects of the job that interviewers will likely explore.

We think you need these skills to ace Principal Investigator - Clinical Trials

In-depth understanding of ICH GCP
Knowledge of FDA regulations
Clinical research ethics
Strong clinical judgment
Attention to detail
Effective communication skills
Flexibility in communication
Medical oversight capabilities
Ability to review and approve study protocols
Experience with patient safety and rights protection
Proficiency in evaluating medical history and conducting assessments
Data interpretation skills (clinical data, lab results, ECGs)
Reporting skills for Serious Adverse Events (SAEs)
Documentation and compliance skills
Understanding of IRB/ethics committee requirements

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 application reflects 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 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.

✨Prepare for Scenario-Based Questions

Expect questions that assess your clinical judgment and decision-making skills. Think of specific scenarios from your experience where you had to evaluate medical histories or manage adverse events, and be ready to explain your thought process.

✨Showcase Your Leadership Experience

Highlight any previous roles where you provided medical oversight or led clinical trials. Discuss how you ensured compliance with protocols and maintained documentation, as this will demonstrate your capability to manage the responsibilities of a Principal Investigator.

Principal Investigator - Clinical Trials
Silver Birch Rec Ltd T/A Etech Partners
S
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