Study Start Up Associate I

As a Study Start Up Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.The SSUA is responsible for leading or supporting operational activities from start-up to close-out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and client standards. Responsibility within a country and may span over more than 1 country depending on the geographical region and business needs.What you will be doing:Clinical Trial Site ActivationInitiate and coordinate activities and essential documents management during start-up towards the compilation of a high-quality Investigator Initiation Package (IIP) leading to approval for site initiation.Register investigator sites and client stakeholders in client registries and systems as required. Update and regularly maintain the registry with accuracy and have it inspection ready.Work directly and interact with investigator sites to confirm readiness for site start-up by reviewing study site profile ready in SIP or reviewing/completing critical information Sheet inclusive of but not limited to Investigator Initiation Packages (IIP) essential documents components, Site contracts contacts, clinical supply shipment information, payment information, IRB submission and status.Take the lead to resolve issues or concerns and timely escalation of Site issues where applicable.Prepare, validate and submit regulatory documents such as completed IIP, IRB approval forms, FDA 1572/Attestation Form, for internal regulatory approval within required timelines.Manage and coordinate with other supporting roles to ensure timely site activation and operational activities.Support the compilation of the Central Investigator Review Board (IRB) package and submissions to approval of the study (where applicable) and other committees as per country requirements.Coordinate the timely communication, documentation and responses between Client and Central Ethics committee to bring clinical study to approval (country dependent).Support investigators sites with local IRB workflow from preparation, submission through approval.Assist with preparation, handling and distribution of non-Clinical Trial Supplies and maintenance of tracking information as needed.Collaborate with the Study Team on the development and readiness of sites eISF when utilized and act as primary point of contact for the sites and manage the Site Operations/CRO monitor access to eISF prior to SIV.Assist with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.Support & implement activities in Shared Investigator Platform to align with client strategy as it relates to the role.Coordinate translation of documents that are within scope with the preferred translation vendors.Clinical Trials ConductPost site activation, initiate and coordinate activities and essential documents management with the investigator’s sites towards the compilation of a high-quality documents and updates through the life cycle of a study such as the documents management for protocol amendments, FDA 1572/Attestation revisions, Ethics Committee annual approvals and other activities required during study conduct.Ensure maintenance of IRB/Ethics and other committees’ activities as applicable.Responsible for timely filing of documents to Trial Master File and assisting with periodic quality review of study files for accuracy and completeness.Accurately update and maintain clinical trial systems that track site compliance and performance within project timelines.Supports investigator sites, and study teams in preparation for and providing responses to site audits / inspections.Internal & External CommunicationMaintain ongoing contact and communication with the study team and respond promptly to study team and investigator site requests.Attend study Start-up meeting and provide functional updates on a country and site level.Establish tools for efficient updates to study team as needed regarding site status, issues, delays, approvals.Disseminate Central or Local Ethics Approval to study team and Investigator Sites where applicable.Communicate Local sites approvals to study team members and stakeholders.Clinical Trial Site SupportAs needed, perform awareness sessions with site personnel on client requirements and to ensure ongoing compliance with study documentation in accordance with prevailing laws, Good Clinical Practices, and Client standards.Identify and resolve investigator site issues within required timeframes; align with study team and local country colleagues on corrective and preventative actions to close open issues and to prevent recurrence / persistence of issues.Additional Responsibilities:A good understanding of the Site Activation requirements and processes within the country/region and be able to learn and potentially implement in more than one (1) country.May be assigned as Study Start Up Associate Point of Contact (PoC) on a study conducted in multi-country.May be assigned as an SME on a system and/or process, and represent the SSUA function as applicable.May represent the SSUA role on global initiatives.Able to act as an SME on projects and initiatives, as requested.Support the mentoring of new hires on processes/ systems.You are:School diploma/certificate with equivalent combination of education, training and experience; BS/BA or bachelor’s degree in life sciences preferred.Minimum 2 years relevant experience in clinical site management.Experience working in the pharmaceutical industry/or CRO in study site activation is an asset.Knowledge of clinical trial methodologies, ICH/GCP, FDA and Global and local country regulations.Must be fluent in Local language and in English. Multilanguage capability is an asset.Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization.Good technical skills and ability to learn and use multiple systems.Demonstrated knowledge of clinical research and development processes, Key operational elements of a clinical trial, and ability to gain command of process details.Understand the quality expectations and emphasis on right first time. Demonstrate compliance with all applicable company, regulatory and country requirements. Attention to detail evident in a disciplined approach.Ability to work independently and also as a team member.Ability to organize tasks, time and priorities, ability to multi-task.Understand basic medical terminology, GCP requirements and proficient in computer operations.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.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.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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