What are the responsibilities and job description for the Feasibility Study Manager position at 1010 Parexel International, LLC?
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. REMOTE - US Feasibility Study Manager Core Job Duties Adapt draft site feasibility questionnaires into electronic survey platform and format Apply appropriate ‘branching’, conditional logic and scoring parameters, as determined by the Feasibility Lead Develop necessary survey reporting templates within survey platform or via external systems as necessary Conduct appropriate quality checks on potential investigators prior to survey outreach Assist in cross-check for available CDAs prior to survey launch Responsible for loading identified site list into survey management system and ensuring all planned investigators for contact are loaded into the applicable survey Responsible for survey launch and regular monitoring & maintenance of survey preparation and management including: Survey Delegation Reconciling survey status Ensuring notes and details are appropriately documents Identification & collation of invalid contact details Proactive research and update invalid or missing contact details to ensure seamless outreach and response efforts and tracking Responsible for reporting and monitoring of country-level responses to aid in early risk and mitigation planning to ensure survey objectives can be met Responsible for execution of agreed site identification strategy, including: Ensuring identification of priority site designation is applied Application of agreed communication strategy and supporting materials (study summary details, communication templates, designated email origin within survey system) Facilitation of revisions to survey content, scoring parameters, and/or site & country list throughout survey duration Monitoring status of site CDA negotiations, and disseminating status updates internally as needed Responsible for survey closure tasks, including but not limited to site notifications Minimum Eligibility Criteria Education: BA or equivalent Year of experience: 3-5 years industry related experience #LI-LG4 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40 years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™