Principal Investigator

The Principal Investigator will serve as the principal leader in a clinical trial setting, taking full responsibility for the oversight and execution of clinical research activities. This role involves ensuring compliance with study protocols, regulatory requirements, and the highest standards of patient care. The Investigator will lead the clinical research team, supervise patient care during trials, and contribute to the advancement of medical knowledge through rigorous study management and professional collaboration.

Key Responsibilities:

• Serve as the primary authority in overseeing and executing clinical trials, ensuring adherence to protocol requirements, regulatory standards, and ethical practices.

• Perform comprehensive physical examinations and assess patients’ medical histories to determine trial eligibility and ensure patient safety.

• Review and analyze lab results and other clinical data to make informed medical decisions and guide trial processes.

• Monitor patient health and safety throughout the trial, addressing adverse events and ensuring adherence to clinical protocols.

• Educate patients and their families about the clinical trial process, potential risks, and expected outcomes.

• Provide direct oversight of medication administration and safety monitoring, including addressing adverse reactions and implementing necessary interventions.

• Collaborate with sponsors, regulatory bodies, and the clinical research team to ensure the effective execution of study protocols and accurate data collection.

• Lead the preparation of clinical documentation, including trial reports, regulatory submissions, and safety evaluations, ensuring accuracy and compliance.

• Supervise and mentor clinical staff, fostering a collaborative and educational work environment.

• Facilitate regular meetings to discuss study progress, patient outcomes, and protocol compliance.

• Stay updated on developments in medical research, regulatory requirements, and best practices in clinical trials, integrating these insights into trial execution.

Additional Responsibilities:

This job description includes core responsibilities but is not limited to the items listed above. The Principal Investigator may also:

• Participate in protocol design and development.

• Provide expert input during regulatory and ethics committee reviews.

• Present research findings at professional conferences and contribute to publications.

• Develop and implement training programs for staff and collaborators.

Medical Specialties:

• Primary Care or relevant specialty related to the clinical trial.

License/Certification Requirements:

• Active Medical License (Required)

Qualifications:

• Proven experience as a clinical investigator or extensive involvement in clinical research.

• Strong leadership skills with the ability to manage and motivate a multidisciplinary team.

• Excellent problem-solving abilities and clinical decision-making skills.

• Exceptional communication and interpersonal skills to effectively interact with patients, families, and collaborators.

• Meticulous attention to detail, ensuring accuracy in documentation and protocol adherence.

• Passion for clinical research, patient advocacy, and the advancement of medical science.

Preferred Skills:

• In-depth knowledge of clinical trial regulations and guidelines (e.g., GCP, FDA, EMA).

• Experience in managing clinical trials from start-up to close-out.

• Familiarity with clinical trial software and data management systems.

Work Environment:

• Collaborative and dynamic research setting.

• Opportunities for professional development, continuing education, and leadership in clinical

Job Type: Full-time

Pay: From $200,000.00 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Work Location: In person

Salary : $200,000