[Hiring] Pharmaceutical Expert @24-MAG

Role Description

We are sharing a specialised consulting opportunity for experienced pharmaceutical professionals with strong expertise in pharmaceutical sciences, clinical pharmacology, drug safety, clinical research, and drug development to contribute to a technology-focused evaluation and content-development project.

Selected professionals will:

• Review pharmaceutical information for scientific and clinical accuracy
• Analyse drug safety and efficacy considerations
• Interpret clinical and pharmaceutical data
• Provide structured expert feedback grounded in established pharmacological and clinical standards

Qualifications

• PharmD, PhD, MD, or equivalent advanced degree in a relevant discipline
• Background in Pharmacy, Pharmaceutical Sciences, Pharmacology, Clinical Pharmacology, or a closely related field
• Professional experience in pharmaceuticals or drug development
• Strong knowledge of clinical research methodologies
• Experience in pharmacology, clinical pharmacology, or pharmacovigilance
• Deep understanding of drug safety and efficacy
• Strong knowledge of pharmacokinetics and mechanisms of action
• Familiarity with indications, contraindications, adverse effects, and therapeutic decision-making
• Experience reviewing pharmaceutical or clinical data
• Ability to interpret scientific and clinical literature
• Strong analytical and critical-thinking capabilities
• Ability to identify scientific or clinical inconsistencies
• Excellent written communication skills
• Ability to provide concise and well-reasoned expert feedback
• High attention to detail across structured evaluation workflows

Requirements

• Independent contractor engagement
• Fully remote
• Compensation: $80–$285/hour
• Work will involve pharmaceutical content review, clinical evaluation, data interpretation, annotation, and quality assessment
• Assignments may cover drug safety, efficacy, pharmacology, pharmacokinetics, mechanisms of action, clinical research, and drug development
• Strong scientific judgement and evidence-based reasoning are central to the engagement
• Contributors may review both structured pharmaceutical data and written clinical or scientific materials
• Project scope and evaluation criteria may vary depending on project requirements
• Clear documentation of findings and reasoning will be expected
• Work must be completed without using confidential, proprietary, patient-identifiable, unpublished clinical, investigational, or otherwise restricted information belonging to any employer, sponsor, healthcare organisation, research institution, client, or other third party