Study Manager

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. Study Manager - Research Collaboration Center of Excellence Primary Duties Operational Study Management for 1 or more studies of limited complexity (e.g. Clinical Research Unit, single country, small number of 3rd party vendors) or manage a unique part of a larger study (e.g. recruitment and retention, 3rd party vendors): Accountable for the development of realistic detailed study startup and monitoring plans Accountable for conducting country level feasibility in collaboration with Global Clinical Trial Execution and CROs, reviewing Pre-trial Assessment outputs, approving sites, and assessing site activation plans Leads study risk planning process in context of site and subject Coordinates study/protocol training & supports investigator meetings Develops and provides key inputs to Clinical Trial Budget (e.g., Per Subject Costs) Accountable for the delivery of the study or subset of agreed study activities against approved plans Leads inspection readiness activities related to study management and site readiness May produce or review model Informed Consent Document (ICD) and study/country/site level ICD, as appropriate May expand study design document into approved protocol template while incorporating input from other team members (e.g., Clinician, Clinical Pharmacology Lead, Supply Chain Lead, Statistician, Outcomes Research Representative, Clinical Assay Group, etc.) Study Management Oversight: Approves the Study Startup, Study Monitoring & protocol recruitment plans Approves & oversees drug supply management – manages flow of drug supply to the sites & set up Interactive Voice Randomization System with Supply Chain Lead Reviews consolidated Pre-trail Assessment reports, feasibility outputs, etc. May support study level submission readiness Study Team Interface: Leads and oversees some or all elements of study startup and monitoring functions both internally and at the CROs to ensure delivery & compliance with all applicable Standard Operating Procedures (SOPs) and Quality Standards, interfacing directly with CRO to determine Feasibility / Study Startup, Monitoring / Management & Site Contracting Groups Works proactively with CRO and data management functions to ensure alignment on data flow and timely delivery Shares and escalates plan deviations to Clinical Project Manager (and study team) May provide ongoing assessment of subject enrollment / discontinuations to inform accurate forecasting for financial planning May provides operational input into protocol design Subject Matter Expertise: The Study Manager will be the technical expert for study management systems and processes The Study Manager will champion the implementation and use of harmonized, consistent processes and excellence in Study Management deliverables related to cost-effective, timely, and high-quality clinical trial data according to agreed global goals. The Study Manager will be responsible for the technical oversight of the CRO to include but is not limited to: mentoring, standards, continuous improvement, issue escalation/resolution, inspection readiness/quality assurance, performance feedback, review of metrics. The Study Manager partners with CRO Managers to proactively identify and resolve study operations staff performance issues. For project-specific audits and inspections, the Study Manager can serve as a resource to the study team to facilitate the audit/inspection. Qualifications Training and Education Preferred: Clinical trial/study management experience Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations BS / Nurse – minimum of 2 years’ relevant experience MS/PhD – minimum of 1 year of relevant experience Prior Experience Preferred: Demonstrated study management experience Experience with CRO oversight Demonstrated experience in managing per subject costs, vendor & ancillary, and monitoring costs projections & spend Skills: Understands how to work with vendors to accomplish tasks Ability to interpret study level data & translate and identify risks Ability to proactively identify & mitigate risks around site level in study execution Understands feasibility of protocol implementation Country level cultural awareness and strong interpersonal skills Keen problem-solving skills Excellent communication skills, both written and verbal. Must be fluent in English. Detail oriented & possesses technical expertise (e.g., spreadsheets, metrics & data flow management) 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. Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.