Senior Registry Manager - CorEvitas

Work ScheduleEnvironmental ConditionsJob DescriptionAt Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life – To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. As part of our clinical research portfolio, our CorEvitas evidence-based solutions specialize in generating data intelligence and clinical insights needed to bring safe and effective treatments to market. Your objectivity and dedication to patient safety will improve health outcomes that people and communities depend on – now and in the future.Location/Division Specific InformationRemote position – Waltham, MA USACorEvitasDiscover Impactful Work:CorEvitas is the built-for-purpose gold-standard provider of real-world evidence. CorEvitas provides a holistic approach to capturing real-world data through patient-centered solutions including clinical registries, patient insight studies, biospecimen solutions and specialty electronic health record (EHR) data. We operate 13 major autoimmune and inflammatory registries across the US, Canada, Europe, and Japan, collecting data from nearly 600 clinical sites.A day in the Life:Responsible for full oversight and management of day-to-day activities within the entire registry, while utilizing key metrics on execution and performance in its entiretyKeys to Success:Works on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors. Exercises judgment in selecting methods, techniques, and evaluation criteria for obtaining results. Networks with key contacts outside own area of expertise.Direct and oversee assigned registry and registry teamMaintain strong relationships with participating sitesEnforce appropriate execution of IRB approved protocol, ensure full regulatory compliance is followed with each site.Ensure and monitor data queries within assigned registries are resolved in a timely mannerStrategize new business development in expansion of participating providers, sites and or registriesSupervising to include Organizing workflow to accomplish established objectives; delegating responsibilities; training, mentoring, and evaluating team member development.Appraise performing sites in a timely yet appropriate mannerSubmit by the 1st of each month key performance indicators of sites participation and enrollment for assigned registry to the Director of Registry Mgt.Work alongside key CorEvitas departments to build out strategies that increase provider and subscriber participation in existing registries and create new opportunities in additional therapeutic areasParticipate in all interactions with current subscribers to appropriately communicate status of enrollment per subscriber agreement. Drive and lead input to desired changes as related to theCorEvitas Registry protocol, questionnaires, site performance metrics and assessments and EDC systemsWork alongside key leadership to balance resource allocation against achievement of company goals.Design and implement recruitment strategies for sites and investigators; work with principal investigators to overcome enrollment barriers and suggest best practicesEducationMaster’s degree, preferably in life sciences, public health, health services research or related area or bachelor’s degree and equivalent experience.Preferred: Advanced degree, Research, and regulatory certifications, i.e., RAPS or ACRP certificatesExperience6 + years’ experience in a clinical research setting.Requires GCP and HSP training certificates per policies and procedures.Knowledge, Skills, AbilitiesExperience analyzing and interpreting written material and quantitative data to draw conclusions and make recommendations based on that data.Demonstrated proficiency in accessing information stored in large data systems. Demonstrated experience using computer applications, including Microsoft Word, Excel spreadsheet and PowerPoint presentation programs, REDCap, Zelta, SalesforceRequires GCP and HSP training certificate per company policies and procedures.Must be able to manage multiple study timelines, sites, and subscriber's commitments.Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As a team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.Apply today! http://jobs.thermofisher.com Thermo Fisher Scientific is an EEO/Affirmative Action Employer