PRN Remote Hematologist

Adams Clinical

11d • $200 - $250 • Remote

About The Position

Adams Clinical is seeking a remote, per-diem Hematologist to provide focused, as-needed consultations for a clinical research site in Dallas, Texas. The role supports a pharmaceutical-sponsored clinical trial and works under the supervision of the physician Principal Investigator and Clinical Operations leadership. The work must comply with FDA regulations, Good Clinical Practice (GCP), study-specific safety guidelines, and institutional policies.

The Hematologist will consult on clinical trial participants who discontinue clozapine because of protocol-defined low neutrophil counts, including severe and applicable moderate neutropenia events. The role includes reviewing blood test results, especially absolute neutrophil count (ANC), assessing clinical findings, recommending appropriate follow-up, and documenting consultations accurately and promptly.

This per-diem position is estimated at less than 1–2 hours per week, with some weeks requiring no involvement. Consultations are scheduled according to study visit windows and clinical needs. Compensation is approximately $200–$250 per hour, commensurate with experience.

Requirements

• Current, unrestricted physician license to practice in Texas.
• Recent experience in clinical practice; outpatient experience is preferred.
• Strong attention to detail and documentation accuracy.
• Ability to document electronically in a variety of systems, such as electronic medical records.
• Ability to collaborate with multidisciplinary teams.
• Excellent organizational, communication, and problem-solving skills.

Nice To Haves

• Clinical research experience is preferred, but not required.
• Outpatient clinical practice experience is preferred.

Responsibilities

• Provide as-needed hematology consultations for trial participants who discontinue clozapine due to protocol-defined low neutrophil counts, including severe neutropenia and applicable moderate neutropenia events.
• Review relevant blood test results, particularly absolute neutrophil count (ANC), and provide clinical assessments and recommendations supporting participant safety, medical follow-up, and study-specific safety compliance.
• Identify and escalate clinically significant findings and changes in participant condition in collaboration with the site Principal Investigator.
• Document assessments accurately and promptly in source records in accordance with study protocols, HIPAA, and ALCOA+ standards.
• Support audit and monitoring readiness.
• Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and institutional policies related to investigational drug services.

What This Job Offers

• Education Level: No Education Listed