Lavori attuali relativi a Clinical Research Associate Iiiii Italy - Bardi - Optimapharm.
-
Bardi, Italia Jr Italy A tempo pienoA leading medical device company in Como, Italy is seeking a Senior Clinical Research Associate to conduct monitoring visits and ensure data accuracy in compliance with regulatory standards.The ideal candidate has at least 5 years of experience in clinical trials and a strong understanding of MDR and ICH/GCP guidelines.This position emphasizes...
-
Bardi, Italia Icon A tempo pienoOverviewDescrizione dell'offerta di lavoroResponsibilitiesA global clinical research organization in Milan is seeking a Clinical Research Associate to manage all phases of clinical trials.This role involves ensuring protocol compliance and data integrity while collaborating with site staff and investigators.QualificationsThe ideal candidate holds a...
-
Bardi, Italia Icon A tempo pienoA leading healthcare-focused organization in Bardi, Italy, is seeking a Clinical Research Associate to oversee clinical trial processes.The role requires a Bachelor's degree in a scientific or healthcare-related field and a minimum of 2 years of relevant experience.Responsibilities include site qualification, data review, and ensuring compliance throughout...
-
Bardi, Italia Jr Italy A tempo pienoA medical device company based in Cremona is seeking a Senior Clinical Research Associate to conduct monitoring visits and ensure compliance with regulatory standards.The ideal candidate should have at least 5 years of experience in clinical trial monitoring, strong organizational skills, and the ability to work independently.This role offers the chance to...
-
Clinical Research Associate
24 minuti fa
Bardi, Italia Tfs Healthscience A tempo pienoOverviewCLINICAL RESEARCH ASSOCIATE - REMOTE BASED (ITALY)TFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey.Our expertise includes full service-capabilities, resourcing and functional service (FSP)...
-
Remote Clinical Research Associate – Oncology Trials
25 minuti fa
Bardi, Italia Tfs Healthscience A tempo pienoA leading global Contract Research Organization is seeking a Clinical Research Associate to remotely monitor clinical trials in Italy.The ideal candidate will have a bachelor's degree, over 2 years of CRA experience in oncology, and strong communication skills.Responsibilities include ensuring compliance with clinical procedures and regulatory...
-
Bardi, Italia Jr Italy A tempo pienoA leading medical device company in Pavia is seeking a Senior Clinical Research Associate to conduct on-site and remote monitoring visits.The ideal candidate has at least 5 years of experience in clinical trials and a strong understanding of compliance with regulatory standards.Responsibilities include training site staff, evaluating data accuracy, and...
-
Senior Clinical Research Associate
24 minuti fa
Bardi, Italia Jr Italy A tempo pienoSocial network you want to login/join with:Senior Clinical Research Associate, cremonacol-narrow-leftClient:TeleflexLocation:Job Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:8556790222002585600337134Job Views:2Posted:**********Expiry Date:**********col-wideJob Description:POSITION SUMMARY:The Senior Clinical Research Associate...
-
Senior Clinical Research Associate
24 minuti fa
Bardi, Italia Jr Italy A tempo pienoSocial network you want to login/join with:Senior Clinical Research Associate, comocol-narrow-leftClient:TeleflexLocation:Job Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:8556790222002585600337126Job Views:2Posted:**********Expiry Date:**********col-wideJob Description:POSITION SUMMARY:The Senior Clinical Research Associate (Senior...
-
Senior Clinical Research Associate
24 minuti fa
Bardi, Italia Jr Italy A tempo pienoSocial network you want to login/join with:Senior Clinical Research Associate, paviacol-narrow-leftClient:TeleflexLocation:Job Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:8556790222002585600337139Job Views:2Posted:**********Expiry Date:**********col-wideJob Description:POSITION SUMMARY:The Senior Clinical Research Associate...
Clinical Research Associate Iiiii Italy
12 ore fa
Location: located in North Italy; MilanWho we areOptimapharm is a globally operating leading mid-sized 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, flexible approach to secure a high level of repeat business, gain the trust of new customers and ensure continued growth of the company.We're expanding our team in Italy and looking for a new CRA (CRA II – III depending on experience).Whether you're building your expertise as a CRA I or ready to step into a higher 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.This role sits within a defined CRA career path: CRA I > CRA II > CRA III > Senior CRA.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 programWho are we looking forQualifications 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 in a CRO/pharmaAt least 15 years of experience in oncology (solid tumors); gastroenterology experience would be considered a plusMandatory: certified CRA in accordance with the Italian Ministerial DecreeHigh level of knowledge of ICH GCP Guidelines, 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, 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 close-out 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 applicableIdentifying and escalating potential risks and identifying retraining opportunities for site personnelPreparation of corrective and preventive (CAPA) plans for issues identified during monitoring activities and proactive follow-up of each individual CAPA until timely resolutionPreparation of 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.Employment Type: Full-TimeVacancy: 1#J-*****-Ljbffr
