Remote Hematologist 2 Hrs Per Wk

Adams Clinical • Dallas, TX

2d • $200 - $250 • Remote

About The Position

Adams Clinical is seeking a remote, PRN/per-diem Hematologist to provide focused, as-needed consultations for its clinical research site in Dallas, Texas. The role supports a pharmaceutical-sponsored clinical trial under the supervision of the physician Principal Investigator and Clinical Operations leadership, following FDA regulations and Good Clinical Practice (GCP) guidelines.

The Hematologist consults on participants who discontinue clozapine because of protocol-defined low neutrophil counts, reviews blood test results—particularly absolute neutrophil count (ANC)—and provides clinical assessments and recommendations to support participant safety, appropriate medical follow-up, and study-specific safety compliance. The role also includes escalating significant findings, documenting assessments accurately and promptly, and supporting audit and monitoring readiness.

This per-diem position is estimated to require less than one to two hours per week, with some weeks requiring no involvement. Consults are scheduled according to study visit windows and clinical needs. Pay is approximately $200–$250 per hour, commensurate with experience.

Requirements

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

Nice To Haves

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

Responsibilities

• Provide as-needed hematology consultations for trial participants who discontinue clozapine because of protocol-defined low neutrophil counts, including severe neutropenia and applicable moderate neutropenia events.
• Review relevant blood test results, particularly ANC, and provide clinical assessments and recommendations to support participant safety, medical follow-up, and compliance with study-specific safety guidelines.
• 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 GCP, FDA regulations, and institutional policies related to investigational drug services.

What This Job Offers

• Job Type: Part-time
• Career Level: Senior
• Education Level: No Education Listed