Linda Richter Email and Phone Number

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• Manage the set-up of studies and sites in the electronic Trial Master File (eTMF)• Manage the creation and distribution of Investigator Site File (ISF) Binders and Pharmacy binders• Liaise with CRAs or CPM to assist with Resolution of site questions• Managed site non-clinical supplies including ordering supplies, initial site shipments, site re-supply requests, and in-house inventory levels• Performed study start-up duties, including but not limited to: essential document collection and review, uploading initial site documents to eTMF, review of site Informed Consent Forms (ICF) against the ICF Checklist, completion of the site IP Release Form, etc.• Uploaded study documents to eTMF as directed by the Clinical Project Manager (CPM)• Performed Quality Control (QC) checks of original documents against electronic copies in eTMF• Created folders and files study documents in paper TMFs, as required• Ensured eTMF Binders are current, accurate, and complete by performing eTMF QC checks• Assisted with meeting set-up, including printing agendas and generating meeting minutes

• Participated in the informed consent process by obtaining subjects’ written informed consent per SOP and IRB guidelines• Conducted study procedures and assessments per protocol• Participated in protocol review and patient retention• Served as liaison between principal investigator, sub-investigator, sponsor, subjects, etc. • Completed case report forms and respond to data queries in a timely manner• Performed accountability of investigational products & reporting temperature excursions • Screened participants for eligibility criteria based on review of medical records, as well as pre-screening potential participants in lieu of recent medical records• Collected and recorded data onto source documents for data entry from participant interviews & procedures (via in-person or phone)• Scheduled participants’ study appointments based on study protocol schedule of activities & procedures• Participated in the preparation or review of documents exchanged within the institutional review board• Performed Electrocardiograms, phlebotomy, physical examinations with participants as per protocol and recorded subject compliance• Obtained medical history and medication usage history with participants, as well as reporting adverse events & serious adverse events to the principal investigator and Institutional Review Board• Processed and shipped human biological samples per protocol, and in compliance with Federal guidelines• Transported investigational products to designated sites or participants as per SOP guidelines• Prepared for and participated in sponsor site initiation visits, routine monitoring visits & study close-out visits• Reviewed & explained consent forms, questionnaires and procedures that established rapport with participants in the presence of the principal investigators or sub-investigators within good clinical practice guidelines• Prepared for and participated in sponsor audits and/or regulatory inspections• Attended sponsor investigator meetings

• Assisted tenured faculty with data entry, data organization, laboratory organization and maintenance.• Instructed undergraduate students with Motor Learning and Control course labs that stimulate the effects of learning, aging and motor control theories. • Piloting/testing out new research studies as budgeted by the department and IRB. • Assisted with faculty and other graduate colleagues on designing research study design, age and target population of participants. • Assisted faculty with preparing for research presentation at South West American College of Sports Medicine (Newport Beach, California).

• Worked with the active elderly patients & elderly patients with Parkinson’s Disease and other movement disorders. • Taught fitness and rehabilitation classes for patients with declined motor function or loss of physical abilities. • Physically spotted and assisted elderly patients with declined or loss of motor function and abilities.• Administered senior fitness testing and assessments are per yearly health guidelines. • Instructed patients on how to operate exercise equipment.• Performed administrative duties and organized patient medical records.