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Coordinate retrospective and prospective project looking at reverse and total shoulder replacement, rotator cuff repair, labrum repair, UCL repair, and various medical device studies Recruit, enroll, consent, follow-up and maintain patient participation in all active studies Complete all regulatory documentation including initial IRB applications, report forms, continuing reviews, amendments and closure forms Work with industry sponsors to initiate new studies and ensure all documents align with study protocols Create informed consent forms, study tracking sheets and case report forms Maintain progress updates of research for study teams Ensure all surveys are completed correctly and study procedures are per the protocol and study design Utilize and build Oncore protocols to track study subjects, follow study visit windows and ensure correct billing Complete IRB submission with the VA Utilize the Advarra payment system Contribute to project development of new studies Review studies annually with department monitors to ensure effective, safe and correct data collection, study and regulatory maintenance.

Research topics include myasthenia gravis, multiple sclerosis, cardiac amyloidosis, stroke, concussion, migraine, CIDP, MMN and epilepsy Perform all study visit requirements per protocol, including informed consent, vitals, anemia levels, ECG, blood draws, medical history, C-SSRS, various questionnaires, ensure eligibility and any other study specific requirements Write, design and implement research protocols, including IRB submission (local and central IRBs including Advarra and WCG), budget, site set up, recruitment materials and informed consent forms Host qualification, initiation, monitoring and closeout visits for commercial trials Process, store and ship all laboratory samples according to study procedures and laboratory manuals Coordinate around seventeen research projects, coordinating with sponsor contacts, vendors, primary investigator, other study staff and enrolled subjects Track study equipment (lab supplies/kits, ECG, incubator, tablets, handheld devices etc) for all studies including receipt, maintenance and return of devices Create all source documentation and ensure timely and accurate data input and query resolution according to ALCOA-C Expert in multiple research vendors including Medidata, Veeva Vault, YPrime, LabCorp, IQVIA, ClinTrak, Cenduit, Clario and a few other study specific sites Perform in depth chart reviews to determine eligibility for interventional, observational and retrospective studies Recruit study participants through in-person, phone and email communication Maintain patient records and investigator site file

Coordinate all research efforts related to the Hamstring Injury Index (HAMIR) study, including all baseline and injury MRIs, hamstring strength measures and sprinting mechanics Collect biomechanical data with inertial movement units Record hamstring strength measurements using the Nordbord device on adolescent and geriatric populations Perform MRI scan on the lower body from T12 to the ankles, ensuring MRI safety, positioning subject in MRI with coils and certify image quality Communicate effectively with primary investigators, study participants, other universities involved with HAMIR (UW-Madison and UNC), external MRI technicians and primary investigators Timely data input and record keeping to ensure accurate information Obtain subject information and informed consent and schedule subjects data gathering for various studies including HAMIR and Hamstring Strength in Older Adults Assist in ultrasound scans of the Achilles tendon in dancers and geriatric populations (CSA, thickness, panoramic, blood flow and elastography) Utilize online storage databases for data transfer between study cites including REDCap, Flywheel and Cloudstor Lead and coordinate a group of 10-15 undergraduate and graduate students to assist in data gathering Recruits and explain consents forms to a geriatric population, including excluding or including subjects based on risk factors