Clinical Research Associate 2
Há 3 horas
Sacavém, Lisboa, Portugal
Alimentiv
Tempo integral
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pAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. /ppAs the world's largest FSP organisation, with over 90 sponsor partnerships,
we offer
stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. /ppAs a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. /ppWhat You Will Do You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. /ppKey Responsibilities Include /ppConducting site qualification, initiation, monitoring, and close-out visits for clinical trials. /ppEnsuring protocol compliance, data integrity, and patient safety throughout the trial process. /ppCollaborating with investigators and site staff to facilitate smooth study conduct. /ppPerforming data review and resolution of queries to maintain high-quality clinical data. /ppContributing to the preparation and review of study documentation, including protocols and clinical study reports /ppYour Profile You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. /ppRequired Qualifications And Experience /ppBachelor's degree in a scientific or healthcare-related field. /ppMinimum of 2 years of experience as a Clinical Research Associate. /ppIn-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. /ppStrong organizational and communication skills, with attention to detail. /ppAbility to work independently and collaboratively in a fast-paced environment. /ppWillingness to travel as required (approximately 60%) /ppWhat ICON Can Offer You Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. /ppIn addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. /ppOur Benefits Examples Include /ppVarious annual leave entitlements /ppA range of health insurance offerings to suit you and your family's needs. /ppCompetitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. /ppGlobal Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. /ppLife assurance /ppFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. /ppAt ICON, inclusion belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. /ppIf, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here /p
we offer
stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. /ppAs a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. /ppWhat You Will Do You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. /ppKey Responsibilities Include /ppConducting site qualification, initiation, monitoring, and close-out visits for clinical trials. /ppEnsuring protocol compliance, data integrity, and patient safety throughout the trial process. /ppCollaborating with investigators and site staff to facilitate smooth study conduct. /ppPerforming data review and resolution of queries to maintain high-quality clinical data. /ppContributing to the preparation and review of study documentation, including protocols and clinical study reports /ppYour Profile You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. /ppRequired Qualifications And Experience /ppBachelor's degree in a scientific or healthcare-related field. /ppMinimum of 2 years of experience as a Clinical Research Associate. /ppIn-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. /ppStrong organizational and communication skills, with attention to detail. /ppAbility to work independently and collaboratively in a fast-paced environment. /ppWillingness to travel as required (approximately 60%) /ppWhat ICON Can Offer You Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. /ppIn addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. /ppOur Benefits Examples Include /ppVarious annual leave entitlements /ppA range of health insurance offerings to suit you and your family's needs. /ppCompetitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. /ppGlobal Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. /ppLife assurance /ppFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. /ppAt ICON, inclusion belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. /ppIf, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here /p