Medical Monitor

We are looking for an additional Medical Monitor to support our growth and strengthen our Medical Affairs team! While our preference is for the ideal candidate to be based in Slovakia, we are open to considering candidates from Czech Republic, Poland, Bulgaria and Romania. Job Responsibilities:The Medical Monitor will provide medical expertise across clinical trials, ensuring subject safety, high-quality data collection, and regulatory compliance. Key responsibilities include:Monitoring trial/subject safety in line with protocol, GCP, and regulatory requirements.Reviewing and evaluating medical data and adverse events, raising queries, and ensuring consistency in clinical trial records.Assessing patient eligibility and supporting study teams with medical questions.Performing second-level review of MedDRA and WHODrug coding to ensure clarity and accuracy.Contributing to study design, conduct, and safety oversight, including participation in project meetings and data safety monitoring boards.Supporting Pharmacovigilance activities and escalating medically relevant issues to sponsors or authorities.Operating in accordance with ICH GCP, GVP, 21 CFR part 11, and relevant regulations. Job Requirements:Completed medical degree. (Mandatory Requirement)Experience in drug safety, clinical development, or medical affairs within the pharmaceutical industry will be considered an advantageKnowledge of ICH GCP, GVP, and PV regulations.Experience with electronic data capture in clinical and safety databases.Familiarity with MedDRA and WHODrug coding practices.Proficiency in English language (level C1 or C2). What We Offer:Competitive salaryFlexible working hours and home-based working optionGreat work-life balance (you will not be overwhelmed with projects as we believe in quality over quantity)Career growth and development opportunities in a continuous learning cultureFriendly environment in a privately owned international companyAdditional paid day off on your birthday You can apply via the link or send a CV directly to: careers@sanaclis.comSanaClis is an equal opportunity and inclusive employer