[Hiring] Pharmaceutical Research & Development Consultant @24-MAG

Role Description

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
• 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.

Qualifications

• 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

Requirements

• 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

Benefits

• 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.

By submitting this application, you acknowledge that your information may be processed by 24-MAG LLC for recruitment and opportunity matching in accordance with our Privacy Policy: https://www.24-mag.com/privacy-policy .