Clinical Trial Manager Posted Date 4 weeks ago(12/9/2024 9:15 AM) ID 2024-115603 Location : Location US-Remote Overview
As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Responsibilities
What you will be doing:
Perform day to day management and oversight of assigned clinical trial(s) to ensure deliverables are met in all phases of trialLead the Clinical Trial Team, and support other development teams as a Clinical Operations representative as requiredPerform and document study level Sponsor Oversight of outsourced clinical activitiesCommunicate study-status, cost and issues to ensure timely decision-making by senior managementInitiate and manage study-level timelines, including communication to internal and external team members on deliverablesWork closely with other supporting clinical operations team members, if applicable, to execute clinical studiesDraft and/or oversee the drafting of site materials including training, manuals and support documentationReview clinical data to ensure timely entry and readiness for data review meetingsPerform periodic review of clinical data, quality metrics and study deviationsManage trial feasibility process and oversee site feasibility/capability assessments in collaboration with the CRO and cross-functional teamReview and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and plans as appropriateReview clinical monitoring reports to ensure timely completion and identification of issuesEnsure trial samples are ready to be sent to vendors in order to meet trial deliverablesComplete and maintain internal clinical trial metrics, dashboards and other internal updatesEnsure trial is conducted in accordance with internal and ICH/GCP standards including multiple regions in global trialsParticipate in testing of clinical trial systems/databases (i.e. UAT)Manage invoice and budget tracking for individual studies and provide input into budget forecasting activitiesMay support additional clinical trial(s) in various capacities (e.g., unblinded clinical trial manager, regional clinical trial manager, etc.)Participate in clinical operations workstreams related to departmental and operating model related initiatives Develop and maintain strong, collaborative relationships with key stakeholders within and externalStrive for continuous improvement and more efficient ways of working in clinical development Qualifications
You are:
minimum of 2+ years of independent trial management preferred
Bachelor’s degree required; Advanced degree preferredRelevant experience in global setting, across more than one phase of development, and across entire lifecycle of a studySolid understanding of drug developmentInfectious Disease experience preferredGood project management skillsGood understanding of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studiesExcellent verbal and written communication skillsGood organizational skills and attention to detail
What 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.
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 others
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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. 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.
https://careers.iconplc.com/reasonable-accommodations
Interested 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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