Job Description

As a Principal Investigator, you will provide clinical mentorship and leadership for clinical development and clinical trials conduct within our organization. You will operate in a wide range of aspects in clinical and pharmaceutical medicine and with patients, health authorities, colleagues, and biopharmaceutical companies. Your role will be focused clinical trials, phase I to IV, where you will be responsible for assessing and following the safety of clinical trial participants and collaborate with the team with all aspects of clinical and scientific input and safety evaluation.

Essential Duties And Responsibilities

• Provide clinical expertise into the conduct of clinical trials
• Build positive relationships and networks with internal and external medical professional and local opinion leaders
• Work closely with colleagues in other functions including, Regulatory Affairs, Clinical Operations and Patient Engagement
• Lead and provide an oversight to a team of researchers and clinical staff involved in conduct of clinical trials
• Be responsible for successful execution of research protocols according to FDA regulations and GCP guidelines
• Evaluate study volunteer’s eligibility for clinical trials
• Perform physical exams and assessments as required per research protocols
• Complete all industry-required training
• Assess study patient health through interviews and physical examinations
• Communicate information to patients regarding diagnosis and treatment goals
• Review all diagnostic reports and provide clinical direction to the study team

Requirements and Qualifications

• 8 years' post training experience as a physician
• Currently licensed to practice medicine in the state of hire with no history of license suspension or department
• Current board certification in specialty area
• Advanced knowledge of treatment and drug interactions
• Ability to build rapport with patients and biopharmaceutical sponsors
• Strong attention to detail
• Strong leadership qualities
• Provide clinical oversight to study team
• Clinical research experience within the last 5 years required