Clinical Research Expert

Alpheva; United States; Remote; USD 234,000 - 303,000; Part time

Job summary

Alpheva is seeking a senior clinical research expert to support AI evaluation projects centered on study protocols, endpoints, bias, safety reporting, and trial interpretation. This is remote, project-based contract work with scope, hours, and assignments determined by project matching.

You will review model responses for missing clinical evidence and unsafe conclusions, and you will write precise reference answers and scoring criteria grounded in protocols.

Qualifications

• 7+ years of substantive experience in clinical research or trial operations.
• Demonstrated senior-level judgment in study protocols, endpoints, bias, safety reporting, and trial interpretation, with substantial responsibility for reviewing or delivering this work.
• Ability to write precise reference answers, assess competing approaches, and justify corrections with traceable evidence.

Responsibilities

• Bring senior clinical research expertise to AI evaluation projects focused on study protocols, endpoints, bias, safety reporting, and trial interpretation.
• Review model responses and worked examples for missing clinical evidence, unsafe conclusions, and uncertainty that is not communicated.
• Write reference answers and scoring criteria grounded in study protocols, endpoints, bias, safety reporting, and trial interpretation.
• Explain consequential errors, evidence gaps, and the reasoning behind your corrections.

Skills

Clinical research expertise

Senior judgment

Traceable evidence

Job description

Bring senior clinical research expertise to AI evaluation projects focused on study protocols, endpoints, bias, safety reporting, and trial interpretation.

Review model responses and worked examples for missing clinical evidence, unsafe conclusions, and uncertainty that is not communicated. Assess whether the reasoning meets professional standards for the stated task.

Write reference answers and scoring criteria grounded in study protocols, endpoints, bias, safety reporting, and trial interpretation. Explain consequential errors, evidence gaps, and the reasoning behind your corrections.

This is remote, project-based contract work. Scope, hours, and assignments depend on project matching; the listed hourly range applies to matched work.

Requirements

• 7+ years of substantive experience in clinical research or trial operations.
• Demonstrated senior-level judgment in study protocols, endpoints, bias, safety reporting, and trial interpretation, with substantial responsibility for reviewing or delivering this work.
• Ability to write precise reference answers, assess competing approaches, and justify corrections with traceable evidence.

Pay

$170-$220/hr

Alpheva is a new expert network (launched September 2026); payout methods are not published yet, so confirm your first payment before scaling up.