Hematologist Clinician

Adams Clinical

2d•$200 - $250•Hybrid

About The Position

Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change. At Adams Clinical, you’ll find: A culture of respect, transparency, and continuous improvement Opportunities for professional growth and learning A team dedicated to improving lives through innovation and integrity. If you’re passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we’d love to have you on our team. Adams Clinical is seeking a Remote Per-diem Licensed Hematologist to provide focused, as-scheduled clinical support for our Texas location. This role works under the supervision of our physician Principal Investigator and Clinical Operations leadership on the conduct of a pharmaceutical-sponsored clinical trial in accordance with FDA regulations and GCP guidelines.

Requirements

Active Texas licensure required
Current, unrestricted Texas license in a qualifying clinical discipline (e.g., physician, psychologist, or psychiatric nurse practitioner) required
This is a per-diem, fixed-term position of 1 day per week for 6 weeks, with hours scheduled based on study visit windows and clinical needs.
Candidates must have the availability to provide remote clinical support across the full 6-week engagement.

Responsibilities

Provide hematology consultations for clinical 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 to support participant safety, appropriate medical follow-up, and compliance with study-specific safety guidelines.
Availability to provide on-site clinical support 1–2 days per week for 6 weeks, as needed to support protocol-required visits. Scheduling will be aligned to protocol visit windows and site needs.
Identify and escalate clinically significant findings and changes in participant condition in collaboration with the site Principal Investigator.
Document assessments in source records accurately and in a timely manner in accordance with study protocols, GCP, HIPAA, and ALCOA+ standards, and support audit and monitoring readiness.