Principal Investigator

Barrington James; Minneapolis (MN); Presencial; USD 150.000 - 210.000; Jornada completa

Descripción de la vacante

Barrington James is seeking an experienced Family Medicine or Internal Medicine physician to join a Minneapolis clinical research site as a Sub-Investigator or Principal Investigator. The role focuses on medical oversight, patient assessments, and trial execution across multiple therapeutic areas.

The ideal candidate will have MD or DO credentials, Minnesota licensure, and prior clinical research experience, with a strong emphasis on ICH-GCP and FDA requirements and collaboration with sponsors

Formación

• MD or DO qualification required.
• Current medical licensure in Minnesota or eligibility to practice in Minnesota.
• Experience in clinical research/clinical trials requested.

Responsabilidades

• Serve as Sub-Investigator or Principal Investigator on studies.
• Provide medical oversight throughout trial lifecycle.
• Oversee patient assessments, medical evaluations and procedures.
• Review patient histories and eligibility criteria.
• Assess adverse events and medical management.
• Review lab, diagnostic and clinical data.
• Ensure patient safety and protocol compliance (ICH-GCP/FDA).
• Engage in meetings with sponsors, CROs and site leadership.
• Collaborate with coordinators and maintain source documents.
• Communicate with stakeholders as required.
• Support recruitment and retention of participants.
• Contribute to resolution of protocol deviations.
• Mentor research team members.

Conocimientos

Family Medicine

Internal Medicine

Clinical Research

MD/DO資格

Educación

MD or DO qualification

Descripción del empleo

Principal Investigator – Clinical Research

Location: Minneapolis, Minnesota

Employment Type: Full-time / Part-time / Flexible

Specialty: Family Medicine / Internal Medicine

Setting: Clinical Research Site

About the Opportunity

A leading clinical research organisation in Minneapolis, Minnesota is seeking an experienced Physician to join its clinical research team as a Sub-Investigator (Sub-I) or Principal Investigator (PI).

This opportunity is well suited to a Family Medicine or Internal Medicine physician with previous clinical research experience who is interested in taking a greater role in the delivery and medical oversight of clinical trials.

The successful physician will work closely with the site's clinical research, regulatory and operations teams, supporting the safe and compliant execution of clinical studies across a range of therapeutic areas.

Key Responsibilities

• Serve as Sub-Investigator or Principal Investigator on assigned clinical research studies, depending on experience.
• Provide medical oversight throughout the clinical trial lifecycle.
• Conduct and/or oversee patient assessments, medical evaluations and study-related procedures.
• Review patient medical histories, eligibility and inclusion/exclusion criteria.
• Assess adverse events and provide appropriate medical management throughout studies.
• Review and interpret laboratory, diagnostic and clinical data.
• Ensure patient safety, protocol compliance and adherence to ICH-GCP and applicable FDA regulations.
• Participate in investigator meetings, site initiation visits and sponsor/CRO interactions.
• Work collaboratively with Clinical Research Coordinators and site leadership to ensure successful study execution.
• Maintain accurate and timely medical documentation and source records.
• Communicate with sponsors, CROs, monitors and other study stakeholders as required.
• Support recruitment, screening and retention of appropriate study participants.
• Contribute to the resolution of protocol deviations and other clinical issues.
• Provide medical guidance and mentorship to members of the research team.

Ideal Candidate

The organisation is particularly interested in physicians with a background in:

• Family Medicine
• Internal Medicine
• General Medicine or closely related specialties

Candidates should have:

• MD or DO qualification.
• Current medical licensure in Minnesota or eligibility to practice in Minnesota.
• Previous experience participating in clinical research / clinical trials.
• Experience as a Sub-Investigator, Investigator, or equivalent clinical research role is highly desirable.
• Strong understanding of ICH-GCP and FDA clinical research requirements.
• Excellent clinical judgement and patient-safety focus.
• Strong communication and interpersonal skills.
• Ability to work effectively with research coordinators, sponsors and CROs.
• A genuine interest in clinical research and advancing new therapies.

Clinical Research Experience

Experience across any of the following would be valuable:

• Phase I–IV clinical trials
• Investigator-initiated studies
• Sponsor/CRO-sponsored research
• Patient recruitment and screening
• Adverse event assessment

  Experience within multiple therapeutic areas is welcomed.

  Why Consider This Opportunity?

  This is an excellent opportunity for a physician who wants to combine their clinical expertise with meaningful involvement in clinical research.

  The successful candidate will have the opportunity to:

  • Take a leading role in clinical trials being conducted in the Minneapolis market.
  • Work alongside an experienced clinical research team.
  • Build on existing Investigator experience and potentially progress toward greater PI responsibility.
  • Work with pharmaceutical and biotechnology sponsors and CROs.
  • Contribute directly to the development of new treatments and therapies.
  • Maintain a strong connection to patient care while expanding their clinical research career.

  Ideal Background

  Family Medicine / Internal Medicine Physician + Clinical Research Experience + Minneapolis/Minnesota

  Candidates with existing Sub-I experience are particularly encouraged to apply, while experienced physicians with strong clinical research backgrounds who are ready to step into a PI role will also be considered.