Physician Principal Investigator (MD or DO)

$225,000 - $250,000/Yr

Ian Martin - Waterbury, CT

Full-time - Senior

Waterbury, CT

Truck Transportation

About the position

The Physician Principal Investigator (MD or DO) is a full-time, permanent role responsible for overseeing sponsor-initiated clinical research trials at CMR's sites in Connecticut. The position involves ensuring adherence to clinical protocols, protecting the rights and welfare of study subjects, and maintaining the integrity of data generated during trials. The Principal Investigator will evaluate potential participants, manage medical care, and represent the company in community outreach activities. This role offers opportunities for professional growth within a leading organization in the Life Sciences industry.

Responsibilities

• Oversee sponsor-initiated clinical research trials at CMR's sites in Connecticut.
• Evaluate potential participants' eligibility for clinical trials.
• Consult with patient recruitment specialists and study coordinators during initial screenings.
• Review and sign-off on subject visits to ensure proper documentation.
• Assess and report any potential adverse events related to investigational products.
• Participate in quality assurance initiatives to improve clinical processes.
• Represent the company at community outreach activities and clinical presentations.
• Assist in evaluating study feasibilities and collaborate with business development staff.
• Maintain investigator qualifications and agreements, including current licensure and training.
• Ensure protocol compliance and ongoing review by a duly constituted IRB.
• Manage the medical care of subjects, including physical exams and reviewing lab results.
• Protect the rights and welfare of subjects by obtaining informed consent and reporting adverse events.
• Ensure validity of data reported to sponsors by maintaining accurate case report forms.
• Document study-related procedures and maintain trial documents as required.
• Direct site clinical operations for assigned clinical trials and meet regularly with the research team.
• Participate in the development of study participation strategies and review protocols for applicability.
• Develop a brand presence and reputation in clinical research through community presentations and digital content.
• Update job knowledge through educational opportunities and professional organizations.

Requirements

• Medical Degree (MD or DO) from a licensed and accredited medical school.
• Board Certification in relevant medical specialty areas, preferably Internal Medicine and/or Endocrinology.
• Extensive experience in sponsor-initiated clinical research trials, ideally over 30 clinical trials as a Principal Investigator.
• At least five years of medical practice experience in a clinical research environment.
• Proficiency in medical software, including eSource, Clinical Trial Management Software, and EHRs.
• Strong understanding of research regulations and standards.

Nice-to-haves

• Experience with common research software used by sponsors/CROs.
• Strong skills in establishing and maintaining effective working relationships with pharmaceutical organizations and the public.

Benefits

• Competitive salary range of $225K - $250K.
• Opportunities for professional development and growth within the organization.