Sarahlena Keckler Email & Phone Number

Miami, Florida, United States

In her role as senior product manager, Sarahlena worked closely with both internal and external stakeholders to translate strategies into deliverables and facilitate the product line life cycle from start (strategic planning) to finish (production delivery), leading innovative development aimed at improving delivery of cancer care to patients while simultaneously adding value to institutional programs by streamlining clinical workflows and reducing provider burden.

Philadelphia, Pa

New study protocol design, development and start-up including: 1) design and creation of all data collection tools and informed consent documents to be consistent with regulatory board requirements and HIPAA policy 2) submission of grant proposals and protocols (with all accompanying documentation) to university scientific review and regulatory boards 3) regular evaluation of regulatory documents, preservation of regulatory binders throughout total study timeframe and availability as principal point of contact for all regulatory board communications, visits and audits. Annual reviews, renewals and modifications to existing protocols for similar review and monitoring processes.Recruitment of study subjects, data collection and coordination of study staff. Tracking of large multi site studies and management and supervision of all study team activities (patient privacy protection and protocol adherence). Facilitate weekly team meetings and regularly presentations of study progress to investigators. Data management and analysis, both quantitative and qualitative. National conference poster presentation developments. Manuscript writing for publications in peer reviewed medical journals.

Responsible for creation and adaptation of data collection tool and informed consent documents consistent with local IRB requirements and HIPAA policy as well as the subject recruitment, data collection and creation and retention of all spreadsheets for tracking data collection for multiple, longitudinal research projects. Additionally assisted in maintaining and updating existing grant proposals with IRB submissions and re-submissions as needed. Managed all study data entry in to quantitative and qualitative data analysis software such as Teleform, N6 NUD*IST, STATA, SPSS and performed preliminary analysis for reporting on study outcomes. Additionally conducted chart reviews and abstractions from EMR records using such programs as Oasis, and UPHS Medview systems and EPIC.Participant at all team meetings ad tracked grant specific budget expenses related to mileage and subject reimbursement for research visits and conducted literature reviews of empirical data as needed.

Bachelor'S Degree, Clinical Psychology

Graduated Cum Laude with a Bachelor's of Science in Psychology

Nursing

Post-Bach core science courses as preparation for accelerated BSN/MSN program