ProTouch Staffing
Title: Clinical Research Endocrinologist
Chicago, IL
Part-Time (0-8 hours/week) About the Role
We are seeking a
Board-Certified Physician
to join as a
Clinical Research Physician
supporting Phase I-IV clinical trials in Chicago, IL. In this role, you will ensure protocol compliance, patient safety, and collaborate with sponsors, CROs, and research teams to advance multi-therapeutic studies. Key Responsibilities
Serve as
Principal Investigator (PI)
or
Sub-Investigator (Sub-I)
for clinical trials.
Conduct medical screenings, physical exams, and assessments of study participants.
Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards.
Collaborate with coordinators, nurses, and research staff to maintain compliance and accurate documentation.
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
Build and maintain strong relationships with sponsors, CROs, monitors, and IRBs.
Participate in site initiation visits (SIVs), monitoring visits, audits, and investigator meetings.
Contribute to feasibility reviews, study design, and recruitment strategies.
Stay current with clinical research regulations and therapeutic advances.
Qualifications
M.D. or D.O. with an active, unrestricted Illinois medical license.
Board Certification
in
Endocrinology .
Valid
DEA license
and
BLS/ACLS certification .
Clinical research/clinical trials experience preferred (training available for motivated candidates).
Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).
Excellent communication, collaboration, and interpersonal skills.
Strong commitment to ethical research and patient-centered care.
Benefits
Flexible, part-time schedule (0-8 hours per week).
Opportunity to expand expertise in multi-therapeutic clinical trials.
Direct involvement in advancing innovative treatments through research.
Chicago, IL
Part-Time (0-8 hours/week) About the Role
We are seeking a
Board-Certified Physician
to join as a
Clinical Research Physician
supporting Phase I-IV clinical trials in Chicago, IL. In this role, you will ensure protocol compliance, patient safety, and collaborate with sponsors, CROs, and research teams to advance multi-therapeutic studies. Key Responsibilities
Serve as
Principal Investigator (PI)
or
Sub-Investigator (Sub-I)
for clinical trials.
Conduct medical screenings, physical exams, and assessments of study participants.
Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards.
Collaborate with coordinators, nurses, and research staff to maintain compliance and accurate documentation.
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
Build and maintain strong relationships with sponsors, CROs, monitors, and IRBs.
Participate in site initiation visits (SIVs), monitoring visits, audits, and investigator meetings.
Contribute to feasibility reviews, study design, and recruitment strategies.
Stay current with clinical research regulations and therapeutic advances.
Qualifications
M.D. or D.O. with an active, unrestricted Illinois medical license.
Board Certification
in
Endocrinology .
Valid
DEA license
and
BLS/ACLS certification .
Clinical research/clinical trials experience preferred (training available for motivated candidates).
Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).
Excellent communication, collaboration, and interpersonal skills.
Strong commitment to ethical research and patient-centered care.
Benefits
Flexible, part-time schedule (0-8 hours per week).
Opportunity to expand expertise in multi-therapeutic clinical trials.
Direct involvement in advancing innovative treatments through research.