Senior Site Management Associate

OverviewAs a Sr Site Management Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doingSupporting and conducting in accordance with the global ISS SOP, EA MAN, and other documentationWorking in partnership with the Manager and cross functional representatives to support timely and appropriate execution of all deliverables (including but not limited to CDA, drug forecasting and re-supply, budget negotiations, fair market value assessment, sponsor/investigator due diligence, regulatory cross reference, contracting, safety data exchange, publications review, and liaising with external vendors)Responsible for tracking and filing of data and documents throughout the processFacilitating review/approval of proposals and protocolsSupporting meetings internally and with sponsors (and or investigators) as appropriateTracking study budget, timeline milestones, and paymentsSupporting set up/conduct/close-out activities, and sponsor (and/or investigator) communicationMay also be assigned a lead role in managing a product-specific ISS programIdentifies and supports resolution of cross-functional issuesParticipates in cross-functional working groupsAssists management in support of activities including process clarification, process improvement, status updates, and metricsMay serve as a point of contact for the Global Development TA, Global Medical Organization and other functional areasMay be responsible for support of training and co-ordination of local Associates/Sr.
AssociatesYou areBasic QualificationsMaster's degree OR Bachelor's degree & 2 years of directly related experience OR Associate's degree & 6 years of directly related experience OR High school diploma / GED & 8 years of directly related experienceExperience supporting Investigator Initiated StudiesPreferred QualificationsBA/BS/BSc in the sciences or RN5 years' work experience in life sciences or medically related field, including at least 2 years of biopharmaceutical clinical research or clinical operations experience (experience obtained working on investigator-sponsored studies)What ICON can offer youOur 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.In 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.Our benefits examples include:Various annual leave entitlementsA range of health insurance offerings to suit you and your family's needsCompetitive retirement planning offerings to maximise savings and plan with confidence for the years aheadGlobal Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-beingLife assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among othersVisit our careers website to read more about the benefits of working at ICON: 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, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, 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 through the form below. in the role, but unsure if you meet all of the requirements?
We would encourage you to apply regardless – there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
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