Study Start Up Associate II

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/79hfdm

ppICON 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. /p pAs a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies. /p h3What You Will Do /h3 pYou will contribute to site start-up and activation activities, taking responsibility for your deliverables and working collaboratively. /p h3Key Responsibilities Include /h3 ul liWork directly with assigned sites on all site related essential document collection and review. /li liPartner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SSU metrics and deliver processes. /li liEnsure standards are applied to the SSU processes across projects. /li liReview site essential documents for start up including but not limited to: ICF, FDF, 1572, CVs etc /li liPromptly recognize and improve potential site activation delays and elevate to appropriate team members. /li liTrack all actions and communications with sites to ensure timelines are achieved for studies and sites assigned. /li liSupport resolving escalated issues identified by the CROs and Clinical Operations teams in partnership with the internal Study Startup team. /li liReview and provide feedback to management on site performance metrics.



/li liEnsure accuracy and completeness of the eTMF for assigned sites during start up /li /ul h3Your Profile /h3 pYou will bring relevant site start-up and activation experience, along with the following qualifications and skills. /p h3Required Qualifications And Experience /h3 ul liBS degree or international equivalent /li li2 or more years of experience in clinical research Site Start Up within a pharmaceutical company, CRO or relevant industry vendor. /li liAbility to explain data to facilitate decision making processes to be data driven. /li liKnowledge and understanding of clinical study protocols and essential documents /li liStrong organizational skills, decision making, communication and negotiation skills /li liProficient in Microsoft Excel, Word, and PowerPoint. /li /ul h3What ICON Can Offer You /h3 pOur 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. /p pIn 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. /p h3Our Benefits Examples Include /h3 ul liVarious annual leave entitlements /li liA range of health insurance offerings to suit you and your family’s needs. /li liCompetitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. /li liGlobal 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. /li liLife assurance /li liFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. /li /ul pVisit our careers site to read more about the benefits ICON offers. /p pAt 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. /p pIf, 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 /p #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/79hfdm