Lavori attuali relativi a Clinical Research Associate Ii/Iii - Bardi - Optimapharm
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Oncology Cra Ii-Iii
59 minuti fa
Bardi, Italia Optimapharm. A tempo pienoA global clinical research organization is expanding its team in Italy and seeks a Clinical Research Associate (CRA II-III).This role offers a unique opportunity to impact patient lives by ensuring high-quality clinical trials.Candidates should have at least 2-3 years of experience in clinical trial monitoring, a relevant degree, and be a certified...
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Bardi, Italia Icon A tempo pienoA leading clinical research organization is seeking a Clinical Research Associate II to play a crucial role in clinical trial design and analysis.This home-based position requires a Bachelor's degree and at least 2 years of CRA experience, with a solid understanding of clinical trial processes.The role involves extensive traveling and offers competitive...
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Clinical Research Associate I/II
4 minuti fa
Bardi, Italia Icon A tempo pienoUn leader nel settore della ricerca clinica con sede in Italia è alla ricerca di un Clinical Research Associate I o II. Il candidato ideale avrà una laurea in un campo scientifico, almeno 2 anni di esperienza e dovrà condurre visite per prove cliniche. La posizione richiede eccellenti capacità organizzative e la capacità di lavorare in modo...
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Bardi, Italia Icon A tempo pienoA leading clinical research organization is seeking a Clinical Research Associate II in Milano, Italy.The role involves conducting site visits, ensuring compliance, and working with clinical data in a fast-paced environment.Ideal candidates hold a Bachelor's in a relevant field and have a minimum of two years' experience in clinical trial processes.The...
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Clinical Research Associate I, Ii Or Senior
2 minuti fa
Bardi, Italia Icon A tempo pienoClinical Research Associate All Levels - São Paulo (FSP - Sponsor Dedicated)ICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking...
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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...
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Bardi, Italia Icon A tempo pienoOverview Descrizione dell’offerta di lavoro Responsibilities A 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. Qualifications The ideal candidate holds a...
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Clinical Research Associate I/Ii
1 ora fa
Bardi, Italia Icon A tempo pienoUn leader nel settore della ricerca clinica con sede in Italia è alla ricerca di un Clinical Research Associate I o II.Il candidato ideale avrà una laurea in un campo scientifico, almeno 2 anni di esperienza e dovrà condurre visite per prove cliniche.La posizione richiede eccellenti capacità organizzative e la capacità di lavorare in modo...
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Clinical Research Associate
1 ora 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)...
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Clinical Research Associate I, Ii Or Senior
4 minuti fa
Bardi, Italia Icon A tempo pienoOverview ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. What you will be doing Conducting site qualification, initiation, monitoring, and...
Clinical Research Associate Ii/Iii
3 ore fa
LocationNorth Italy, MilanWho we are?Optimapharm 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 optimal access to patients and investigators worldwide.Established nearly 20 years ago, we leverage our experience, stable project teams and a collaborative, flexible approach to secure a high level of repeat business, gain the trust of new customers and continue to grow.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 offer?Working 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 for?Qualifications 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 1.5 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, knowledge of regulatory requirements and a strong interest in clinical researchComputer proficiency is mandatoryAbility to read, analyse 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 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 applicableIdentifying and escalating potential risks and identifying re-training opportunities for site personnelPreparation of corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active 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-g 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
