Location: Spain (Madrid or Barcelona based)Who we are?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 general reach with the agility, collaboration, and supportive culture of a mid-sized organisation. Here, your expertise is valued, your growth is encouraged, and your work has a visible impact.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 . At Optimapharm, your dedication is rewarded with meaningful growth opportunities, exposure to diverse studies, and the support needed to reach your full potential.What do we offer?Working in a successful company that’s growing and developing every dayBeing part of a clinical research team that transforms science into hope for patientsInternational projects and professional growthPerformance bonusReferral bonusFlexible work hoursWork from home allowanceAdditional Health InsuranceShopping discountsEmployee engagement programsWell-being initiativesTraining and development programWho are we looking for?Qualifications And ExperienceUniversity degree in medicine, pharmacy, dentistry, or equivalentAt 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 processKnowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirementsFluent in local language and English, both written and verbalComputer proficiency is mandatoryAbility to read, analyze, and interpret common scientific and technical journalsExcellent verbal and written communication skillsExcellent interpersonal and negotiation skillsAbility to work with minimal supervision, pro-activeAffinity to work effectively and efficiently in a matrix environmentExcellent numerical skills and reasoning abilityA current, valid driver's licenseYour responsibilitiesPerform routine site visits independently, including pre-study, initiation, interim monitoring and closeout visits across the regionManage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirementsIndependently perform CRF review; generate and resolve queries against established data review guidelines or data management systems as applicableIdentify and escalation potential risks and identify retraining opportunities for site personnelPrepare corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active follow-up on each individual CAPA until timely resolutionPrepare documents required for EC submissions and notifications, translate study-related documents (where applicable), and perform other tasks as instructed by the supervisorIndependently negotiate study budgets with potential investigators and institutions and assist with the execution of site contracts as applicableSupport administration of site payments in accordance with relevant project instructionsCompensation is competitive and final offers will reflect each candidate's experience, skills, and qualifications.
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📌 Senior Clinical Research Associate - Spain (Madrid)
🏢 Tamarind Intelligence
📍 Madrid