Optimapharm is a mid-sized, global Contract Research Organisation turning science into hope through agile, patient-focused clinical development. At Optimapharm, you'll have the opportunity to work on diverse and meaningful projects that help bring innovative therapies to patients worldwide. As part of our international team, you'll collaborate with experts across multiple disciplines, gain exposure to a broad range of therapeutic areas, and contribute to research that makes a real difference.

With colleagues in 26 countries and operations in more than 40 countries, we combine global reach with the agility, collaboration, and supportive culture of a mid-sized organisation. We're searching for a CRA who is motivated by quality, driven by purpose, and eager to contribute to innovative clinical research that changes lives . Being part of a clinical research team that transforms science into hope for patients International projects and professional growth Performance bonus Adaptable work hours Work from home allowance Additional Health Insurance Well-being initiatives Training and development program University degree in medicine, pharmacy, dentistry,



or equivalent At least 4 years of independent clinical trial monitoring experience (oncology, neurology, infectious diseases experience is a plus) Strong interest in clinical research and excellent understanding of the clinical trial process Fluent in local language and English, both written and verbal Ability to work with minimal supervision, pro-active A current, valid driver's license Perform routine site visits independently, including pre-study, initiation, interim monitoring and closeout visits across the region generate and resolve queries against established data review guidelines or data management systems as applicable Prepare corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active follow-up on each individual CAPA until timely resolution Independently negotiate study budgets with potential investigators and institutions and assist with the execution of site contracts as applicable Support administration of site payments in accordance with relevant project instructions

📌 Senior Clinical Research Associate - Spain (Madrid)
🏢 Tamarind Intelligence
📍 Madrid