Senior Clinical Research Associate Italy

Location :located in North Italy; MilanWho we areOptimapharm is a globally operating leading mid-size full-service CRO aiming to deliver new therapies to improve and save patients lives.Optimapharm's key priorities are the well-being of our people, consistent quality delivery to our clients and healthy sustainable growth.With 26 strategically located offices Optimapharm operates in 40 countries, providing the most optimal access to patients and investigators globally.Established nearly 20 years ago, we leverage our experience, stable project teams and collaborative and flexible approach to secure a high level of repeat business, gain the trust of new customers and secure continued growth of the company.We're expanding our team in Italy and looking for a new CRA (CRA III – Senior CRA depending on experience).Whether you're building your expertise as a CRA II or ready to step into a Senior CRA role, this is your chance to shape the future of clinical research – delivering excellence for our sponsors and meaningful impact for patients and families worldwide.What do we offerWorking in a successful company that's growing and developing every dayWorking with a highly experienced team of clinical research professionalsPerformance bonusReferral bonusFlexible work hoursHome-based positionWorking from home allowanceMeal vouchersShopping discountsEmployee engagement programsWell-being initiativesTraining and development programQualifications and ExperienceUniversity degree preferably in medical or life sciences; nursing education or other relevant healthcare college degreeAt least 2–3 years of independent clinical trial monitoring experience in oncology (solid tumors); gastroenterology experience would be considered a plusHigh level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements and a strong interest in clinical researchComputer proficiency is mandatoryAbility to read, analyze and interpret common scientific and technical journalsExcellent verbal and written communication skillsVery good interpersonal and negotiation skillsAbility to work independently and pro-activeAffinity to work effectively and efficiently in a matrix environmentA current valid driver's licenceYour responsibilitiesPerform routine site visits independently including pre-study initiation, interim monitoring and closeout visitsManage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirementsIndependently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicableIdentify and escalatie 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 of each individual CAPA until timely resolutionPrepare documents required for EC submissions and notifications, translation of study-related documents (where applicable) and other tasks as instructed by the supervisorIndependently negotiate study budgets with potential investigators/institutions and assist with the execution of site contracts as applicableAdministration of site payments in accordance with relevant project instructionsBy joining our fast-growing and prosperous team you will have an excellent opportunity for further personal growth and career development.If you would be interested in joining the Optimapharm team please send your CV and note that only shortlisted candidates who meet the requirements will be contacted for the further selection process.Compensation is competitive and final offers will reflect each candidate's experience, skills and qualifications.Disclaimer :Unsolicited CVs sent to Optimapharm (Talent Acquisition Team Hiring Managers or any other OPT employee) by recruitment agencies will not be considered for this role.Optimapharm follows a direct sourcing strategy and collaborates exclusively with selected recruitment partners when external support is required.#J-*****-Ljbffr