Manage and oversee multiple trials, ensuring all start-up activities are complete, including completion of feasibilities, pre-study and site initiation visits.▪ Manage phase 1- phase 3 indication specific oncology trials, including all Hematological Malignancies, Gynecological, Genitourinary, Lung, and Head and Neck. ▪ Provides oversight and site management to ensure that supplies are secured, documentation is complete, and staff has necessary studies accesses.▪ Seek out potential trials according to Principle Investigators interests and indication gaps.▪ Assist in preparation and participation in Sponsor, FDA and NRG driven audits.▪ Work with CROs/Sponsor to develop and initiate working relationships.▪ Experience working with Global sponsors▪ Oversee project progress and closeout procedures.▪ Serve as a research meeting liaison and meet with medical science liaisons for trial progress and new opportunities. Work with legal, finance, and regulatory teams to open trials.▪ Attend and prepare agendas for indication-specific subgroup meetings.▪ Run reports for partnership relationship meetings, new staff, and study related metrics.▪ Review and edit initial regulatory documents, including consents.▪ Communicating quality improvement to enhance implementation and management▪ Performs essential document collection▪ Knowledge of ICH and GCP guidelines

Provide support to the research team by collecting, entering, abstracting, and managing the study data for sponsor data systems, publication, or other reporting. Assists in the set-up and execution of clinical research protocol procedures and associated administrative responsibilities. Coordinate retrospective, quality, and other non-therapeutic research trials under Principal Investigator direction. Responsible for maintaining research medical equipment; accurately maintain logs; perform protocol-related tasks as assigned, inventory, store, order and maintain study-related equipment/ supplies.

Provide support for research initiatives, protocol management, and study coordinator meetings. Schedule study participant appointments and serves as the patient liaison to the PI. Conducts patient recruitment and enrollment, patient follow up, data collection, sample/specimen collection and reporting. Collects, compiles, and organizes research data. Create standard operations procedures, along with study specific documents.

Actively market and recruit appropriate clients to participate in research interventions using investigational medications. Assist with research startups, and source documents. Responsible for excel sheets containing weekly and monthly data.

Served as a supervisor and manager to a team of activity based techs in a physical therapy setting, created and managed an excel database of current and past patient outcome measures from the clinic and research data. Created and administered trainings for new hires and current employees in order to stay up to date with new equipment, assisted in coordinating outreach and program events. Additional duties include assisting in Research protocols, data collection and analysis, managing projects, and adhering to timelines.