Clinicia Expert - Remote

Job Description

Job Description

Job Title: Clinician Expert Remote

Job Type: Contractor
Location: Remote

We are seeking experienced Clinicians specializing in Oncology and Hematology to contribute their medical expertise to an innovative healthcare AI project. In this role, you will help improve next-generation AI systems by evaluating clinical content, reviewing trial data, and providing expert medical judgment. No prior AI experience is required—your clinical expertise and domain knowledge are what matter most.

• Author and review clinical evaluation tasks requiring advanced oncology and hematology expertise.

• Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess medical accuracy.

• Evaluate the clinical relevance of efficacy and safety conclusions, including endpoints and treatment outcomes.

• Assess dose escalation strategies, dose-limiting toxicities, adverse event grading, attribution, and patient safety narratives.

• Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible interpretations.

• Provide structured, guideline-based written explanations of clinical reasoning and findings.

• Support AI model training by delivering high-quality clinical evaluations and expert feedback.

• Clinical Oncology

• Clinical Hematology

• Clinical Trial Evaluation

• CTCAE Grading

• RECIST

• Lugano Criteria

• IMWG Criteria

• IWCLL Criteria

• ELN Criteria

• Outcome Endpoint Analysis (ORR, DoR, PFS, OS, MRD)

• Dose Escalation Assessment

• Adverse Event Grading & Attribution

• Board certification or specialist registration in Medical Oncology and/or Hematology.

• 5+ years of post-training clinical experience.

• Direct experience with clinical trials as an investigator, sub-investigator, medical monitor, safety physician, or clinical development physician.

• Experience reviewing clinical trial documents, including protocols, investigator brochures, clinical study reports, safety narratives, and DSMB/IDMC materials.

• Strong understanding of oncology and hematology response criteria and clinical endpoints.

• Excellent written communication skills with the ability to explain complex clinical concepts clearly.

• Experience in medical monitoring, medical director roles, adjudication committees, or independent review committees is preferred.

• Peer-reviewed publications or authorship of clinical trial manuscripts is a plus.

• Experience with AI-assisted clinical review tools is an advantage.