Drug Safety Specialist

A leading AI-focused organization is seeking experienced Pharmaceutical Experts to contribute their expertise to the development and evaluation of next-generation AI systems. In this role, you will apply your knowledge of pharmaceuticals, pharmacology, clinical research, drug development, and drug safety to assess, refine, and create high-quality pharmaceutical content used in AI training and evaluation.

Siga leyendo para descubrir lo que necesitará para tener éxito en este puesto, incluyendo habilidades, cualificaciones y experiencia.

This opportunity is ideal for professionals with experience in pharmacy, pharmaceutical sciences, clinical pharmacology, pharmacovigilance, clinical research, or drug development. You will help ensure that AI-generated pharmaceutical content reflects scientific accuracy, evidence-based medicine, and real-world industry standards.

The work is fully remote, flexible, and focused on practical pharmaceutical and clinical applications. No prior AI experience is required.

Key Responsibilities

• Review and evaluate pharmaceutical and drug-related content for scientific, clinical, and regulatory accuracy.
• Assess information related to drug safety, efficacy, indications, contraindications, dosing, and adverse events.
• Apply expertise in pharmacology, pharmacokinetics, pharmacodynamics, and mechanisms of action to real-world scenarios.
• Analyze clinical research materials, study findings, and drug-development documentation.
• Evaluate AI-generated pharmaceutical content and provide structured feedback on accuracy, clarity, and completeness.
• Interpret pharmaceutical, clinical, and scientific data and communicate findings clearly.
• Identify inaccuracies, inconsistencies, unsupported claims, and potential safety concerns.
• Complete structured evaluation, annotation, and quality-review tasks using professional pharmaceutical expertise.
• Contribute expert insights that improve AI performance in pharmaceutical and healthcare-related domains.

Required Qualifications

• Advanced degree in Pharmacy, Pharmaceutical Sciences, Pharmacology, Clinical Pharmacology, Medicine, or a closely related field.
• Professional experience in pharmaceuticals, clinical research, drug development, pharmacovigilance, regulatory affairs, or related areas.
• Strong understanding of drug safety, efficacy, pharmacokinetics, pharmacodynamics, and mechanisms of action.
• Experience reviewing scientific literature, clinical research, or pharmaceutical data.
• Excellent analytical and critical-thinking skills.
• Ability to work independently in a remote environment.
• Strong attention to detail and commitment to evidence-based evaluation.

Preferred Qualifications

• PharmD, PhD, MD, or equivalent advanced professional qualification.
• Experience in pharmaceutical industry, biotechnology, CROs, regulatory agencies, academic research, or healthcare organizations.
• Background in clinical trials, pharmacovigilance, medical affairs, regulatory submissions, or drug safety monitoring.
• Experience interpreting clinical study results and scientific publications.
• Familiarity with FDA, EMA, ICH, or other pharmaceutical regulatory frameworks.
• Experience developing educational, scientific, or healthcare-related content.
• Interest in healthcare technology, digital health, or AI-assisted medical applications. xqbhyrx

Compensation

• $80–$285/hour
• Performance-based project opportunities

Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.