Remote

We are sharing a specialised part-time consulting opportunity for professionals experienced in pharmaceutical documentation, clinical trial materials, study protocol review, regulatory-style records, clinical research workflows, instruction-based task design, and structured evaluation.

This role supports current and upcoming remote consulting opportunities focused on AI-assisted review of pharmaceutical and clinical research documents, forms, tables, study materials, and related visual content. Selected professionals will create complex evaluation tasks using clinical trial and pharma-related materials, define clear expected answers, and develop objective rubrics for assessing response accuracy, instruction alignment, and domain understanding.

Key Responsibilities

Professionals in this role may contribute to:

Clinical Research Task Development

• Create complex tasks based on clinical trial protocols, study forms, patient-facing materials, investigator documents, tables, charts, and pharma-related records
• Define clear ground-truth answers, acceptable response criteria, and objective evaluation standards
• Develop prompts that test study document interpretation, protocol reasoning, information extraction, data review, and careful instruction following
• Ensure each task is clearly scoped, realistic, and suitable for structured review workflows

Pharma & Trial Document Review

• Evaluate AI-generated responses involving clinical research documents, pharmaceutical materials, study records, forms, tables, diagrams, and trial-related content
• Assess whether responses correctly interpret study criteria, protocol details, timelines, dosage information, adverse event references, visit schedules, and document-specific instructions
• Identify missing details, incorrect interpretations, unsupported assumptions, weak reasoning, or inconsistencies in the response
• Review outputs against objective rubrics and project-specific quality standards

Rubric Design & Quality Control

• Develop clear rubrics that explain expected answers, grading criteria, and acceptable variations
• Provide structured written feedback on task quality, response accuracy, and evaluation consistency
• Apply detailed instructions carefully across pharmaceutical, clinical trial, and document-based review tasks
• Participate in onboarding, calibration, or domain alignment activities when required

Ideal Profile

Strong candidates may have:

• Professional experience in clinical research, pharmaceuticals, clinical trials, regulatory operations, medical writing, study coordination, pharmacovigilance, or related documentation work
• Strong ability to interpret study protocols, trial forms, clinical research tables, eligibility criteria, safety documentation, and pharma-related records
• Comfort working with precise instructions, objective criteria, and structured evaluation standards
• Strong written communication skills with the ability to explain task expectations and review decisions clearly
• High attention to detail when assessing accuracy, completeness, and instruction alignment
• Ability to work independently in a remote, project-based environment
• Consistency across repetitive, detail-oriented review and rubric-based evaluation tasks

Educational Background

• Academic or professional background in pharmacy, clinical research, life sciences, biomedical sciences, nursing, medicine, public health, regulatory affairs, or a related field is highly relevant
• Experience with clinical trial protocols, informed consent materials, case report forms, study schedules, regulatory-style documentation, safety records, or pharma documentation may be especially valuable
• Training or professional experience involving clinical research operations, medical documentation review, trial coordination, regulatory review, data quality, or structured assessment is relevant
• Advanced clinical research, pharmaceutical, regulatory, medical writing, or study operations experience may support project fit depending on scope

Nice to Have

• Experience creating assessment tasks, training materials, documentation standards, review guides, or structured evaluation rubrics
• Familiarity with clinical trial phases, protocol design, inclusion and exclusion criteria, adverse event reporting, study visit schedules, or regulatory documentation
• Experience reviewing protocols, case report forms, informed consent documents, tables, charts, safety narratives, or clinical research datasets
• Comfort identifying ambiguity, missing information, unsupported assumptions, inconsistent study logic, or interpretation errors
• Strong ability to design objective criteria for evaluating complex clinical research or pharmaceutical document reasoning tasks

Why This Opportunity

• Apply clinical research and pharmaceutical documentation expertise to structured remote project work
• Contribute to high-quality pharma and clinical trial document review, task development, and rubric-based evaluation
• Use protocol interpretation, research documentation review, and evaluation design skills in a focused project environment
• Work on flexible assignments aligned with clinical trial, pharma, regulatory, and structured assessment strengths
• Remote structure with competitive hourly compensation

Contract Details

• Independent contractor role
• Fully remote with flexible scheduling
• Eligible professionals may be based in approved project locations, including Canada and the United States, depending on project needs
• Part-time commitment, with an estimated 15–20 hours per week depending on project availability and onboarding status
• Competitive rates up to $40 per hour depending on expertise, clinical research or pharmaceutical background, task quality, and project scope
• Weekly payments via Stripe or Wise
• Projects may be extended, shortened, or adjusted depending on scope and performance
• Work will not involve access to confidential or proprietary information from any employer, client, or institution

About the Platform

This opportunity is available through 24-MAG LLC. We connect experienced professionals with remote consulting opportunities across technical, evaluation, and project-based workstreams.

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