We are sharing a specialised part-time consulting opportunity for professionals experienced in pharmaceutical research, drug discovery, translational science, clinical development, regulatory documentation, CMC workflows, and structured pharma R&D processes.

This role supports current and upcoming remote consulting opportunities focused on structured pharmaceutical research review, clinical development workflow analysis, regulated R&D documentation, study protocol assessment, biomarker and pharmacology review, regulatory materials, and high-quality project execution. Selected professionals will apply their pharma, biotech, or academic research expertise to review realistic R&D scenarios, evaluate documentation requirements, prepare structured written outputs, and support accurate, evidence-based pharmaceutical research workflow tasks.

Key Responsibilities

Professionals in this role may contribute to:

Drug Discovery & Translational Research Review

• Review pharmaceutical research scenarios involving target identification, medicinal chemistry, biology workflows, high-throughput screening, DMPK, PK/PD, toxicology, and biomarker analysis
• Evaluate research materials against source documents, study requirements, experimental rationale, data outputs, and documented scientific criteria
• Support structured review of pharmacology reports, biomarker analyses, preclinical documentation, translational research materials, and lab workflow records
• Identify missing assumptions, documentation gaps, scientific inconsistencies, and expected research review outcomes

Clinical Development & Study Documentation

• Review clinical development scenarios involving study protocols, investigator brochures, Phase I–IV materials, clinical operations workflows, statistical outputs, and study documentation
• Evaluate clinical materials against required sections, source materials, study objectives, endpoint definitions, and operational requirements
• Support structured review of DMC briefing documents, clinical study reports, protocol summaries, clinical operations files, and study-related documentation
• Prepare clear written explanations for clinical development decisions based on source materials and verifiable criteria

Regulatory, CMC & R&D Workflow Support

• Review regulatory and CMC scenarios involving IND, NDA, BLA, EMA materials, CMC technical reports, quality documentation, safety materials, and submission workflows
• Support structured review of real-world evidence, HEOR, pharmacovigilance, regulatory affairs, and CMC documentation
• Work with materials connected to platforms such as Medidata Rave, Oracle Clinical One, Schrödinger Suite, MOE, Benchling, LabArchives, or similar pharma R&D systems
• Maintain accuracy, consistency, and professional judgment across submitted work

Ideal Profile

Strong candidates may have:

• 3+ years of experience in pharmaceutical research, biotech research, drug discovery, translational science, clinical development, regulatory affairs, CMC, pharmacovigilance, HEOR, or academic biomedical research
• Background in one or more areas such as target identification, medicinal chemistry, biology, HTS, DMPK, PK/PD, toxicology, biomarkers, clinical development, biostatistics, clinical operations, regulatory affairs, CMC, real-world evidence, or pharmacovigilance
• Familiarity with pharma R&D tools and platforms such as Medidata Rave, Oracle Clinical One, Schrödinger Suite, MOE, Benchling, LabArchives, electronic lab notebooks, clinical data systems, or related research systems
• Comfort reading and preparing pharma research artifacts such as study protocols, investigator brochures, IND/NDA/BLA materials, pharmacology reports, biomarker analyses, CMC reports, DMC briefing documents, and research summaries
• Strong analytical thinking and written communication skills
• Ability to translate pharmaceutical R&D workflows into clear, structured task documentation

Educational Background

• PhD, MD, PharmD, or master's degree in pharmaceutical sciences, biomedical sciences, biology, chemistry, pharmacology, medicine, biostatistics, regulatory affairs, clinical research, or a related field is helpful
• Equivalent practical experience in pharmaceutical research, clinical development, translational science, regulatory documentation, or biotech R&D workflows is also highly relevant

Nice to Have

• Experience in pharma, biotech, academic medical centers, clinical research organizations, regulated R&D environments, or major biomedical research programs
• Familiarity with IND, NDA, BLA, EMA submissions, CMC documentation, clinical trial operations, pharmacovigilance, HEOR, real-world evidence, or DMC materials
• Experience preparing or reviewing study protocols, investigator brochures, pharmacology reports, biomarker analyses, CMC technical reports, regulatory drafts, or clinical development documentation
• Industry fellowship training, clinical research certification, regulatory affairs certification, or related specialized training is helpful
• Strong attention to detail in scientific, regulated, and documentation-heavy research environments

Why This Opportunity

• Apply pharmaceutical research and clinical development expertise to structured remote project work
• Contribute to high-quality R&D workflow review, clinical documentation assessment, regulatory materials, and scientific scenario development
• Work on flexible, project-based assignments aligned with your pharma or biotech background
• Use your scientific judgment in a focused, detail-oriented research environment
• Remote structure with competitive hourly compensation

Contract Details

• Independent contractor role
• Fully remote with flexible scheduling
• Part-time commitment depending on project availability
• Competitive rates between $65–$90 per hour depending on expertise
• 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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