Job Description
Job Title: Pharma/Biotech Expert Evaluator Job Type: Contract, Part-time Location: Remote Job Summary: Join our customer's team as a Pharma/Biotech Expert Evaluator, where you will leverage your advanced scientific expertise to assess cutting-edge pharmaceutical and biotechnology research. This is a unique opportunity to influence the quality and integrity of research in a dynamic, remote environment, collaborating with leading professionals in the field. Key Responsibilities: β’ Critically evaluate scientific materials, research summaries, experimental designs, and clinical trial data for rigor, accuracy, and clarity. β’ Assess the depth of scientific reasoning, domain expertise, and problem-solving across drug discovery, preclinical, and clinical development stages. β’ Review, critique, and synthesize scientific literature, mechanisms of action, and study methodologies with attention to regulatory relevance. β’ Apply industry-standard frameworks (FDA, EMA, ICH) to the evaluation of clinical and nonclinical documentation. β’ Identify methodological strengths and weaknesses, providing actionable, structured feedback based on established scientific and regulatory standards. β’ Collaborate with the customer's team to uphold high standards of research evaluation and domain-specific knowledge. β’ Communicate findings effectively through clear, precise written and verbal reports. Required Skills and Qualifications: β’ PhD in pharmacology, biochemistry, molecular biology, drug discovery, or a closely related discipline; OR MS/BS with commensurate experience. β’ Minimum 5 years of experience in pharmaceutical or biotech R&D settings. β’ At least 3 years of hands-on experience in drug discovery, preclinical/clinical development, or biotech research. β’ Expertise in at least two areas: drug discovery/target validation, clinical trials, PK/PD, medicinal chemistry, biologics/cell & gene therapies, regulatory affairs, or drug safety/toxicology. β’ Comprehensive understanding of FDA and EMA regulatory frameworks and documentation. β’ Exceptional critical evaluation and data interpretation skills, with the ability to discern methodological soundness. β’ Outstanding written and verbal communication abilities, essential for delivering high-quality feedback and collaborating remotely with the team. Preferred Qualifications: β’ Peer-reviewed publication record in pharmaceutical or biotechnology research. β’ Experience authoring or reviewing regulatory documentation (e.g., IND, IMPD, CTD). β’ Background in mentoring, teaching, or evaluating scientific talent. Apply tot his job