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Title

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Drug Evaluator

Description

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We are looking for a highly qualified Drug Evaluator to join our pharmaceutical research and development team. The ideal candidate will be responsible for analyzing, evaluating, and documenting the safety, efficacy, and quality of new drugs before their approval and commercialization. This role is essential to ensure that pharmaceutical products meet regulatory and scientific standards set by national and international health authorities. The Drug Evaluator will work closely with multidisciplinary teams, including scientists, physicians, regulators, and manufacturers, to review clinical and preclinical data, conduct risk-benefit assessments, and prepare detailed technical reports. Additionally, they will participate in the development of study protocols, oversee clinical trials, and assist in the preparation of documentation for regulatory approval. This position requires a deep understanding of pharmacology, toxicology, biostatistics, and regulatory frameworks. Experience in clinical research and the ability to interpret complex scientific data are also highly valued. The candidate must possess exceptional analytical skills, attention to detail, and a strong professional ethic. The Drug Evaluator plays a key role in protecting public health by ensuring that medications available on the market are safe and effective for patients. If you are passionate about science, rigorous analysis, and making a positive impact on global health, this is an excellent opportunity for you.

Responsibilities

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  • Evaluate the safety and efficacy of new drugs.
  • Review clinical and preclinical data.
  • Collaborate with multidisciplinary teams.
  • Prepare detailed technical reports.
  • Oversee clinical trials.
  • Ensure compliance with regulatory standards.
  • Conduct risk-benefit analyses.
  • Participate in the development of study protocols.
  • Interpret complex scientific data.
  • Contribute to drug regulatory approval processes.

Requirements

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  • University degree in Pharmacy, Medicine, Biology, or related field.
  • Experience in drug evaluation or clinical research.
  • Knowledge of regulatory standards (FDA, EMA, etc.).
  • Analytical skills and attention to detail.
  • Ability to work in multidisciplinary teams.
  • Proficiency in statistical tools and scientific software.
  • Excellent written and verbal communication skills.
  • Professional ethics and confidentiality.
  • Ability to manage multiple projects simultaneously.
  • Advanced level of technical English.

Potential interview questions

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  • What is your previous experience in drug evaluation?
  • Have you worked with international regulatory standards?
  • What statistical tools are you proficient in?
  • How do you handle the interpretation of complex clinical data?
  • Have you participated in clinical trials?
  • How do you ensure quality and accuracy in your reports?
  • Are you familiar with drug approval processes?
  • What motivates you to work in this field?
  • How do you handle tight deadlines?
  • Do you have experience working with multidisciplinary teams?