Molly Johnson Email & Phone Number

Indianapolis, Indiana, Us

• Guiding clinical trial teams and investigators through the transition from investigational product to commercial product• Writing, implementing, and managing Clinical Trial protocols • Creating, approving, and maintaining budgets for Clinical Trial Sites• Co-Chair for the Avid Chapter of Women’s Initiative for Leading at Lilly (WILL)• Informed Consent Subject Matter Expert writing, reviewing, and approving Informed Consent Forms for clinical trial sites

Indianapolis, Indiana, Us

• Assisted in closing out Phase III Clinical Trials for the submission and approval of a New Drug Application to the United States Food and Drug Administration (U.S. FDA)• Expanded and maintained the Exploratory Investigator Sponsored Trial and Investigator Initiated Trial (ExIST and IIT) Program• Continued role as Informed Consent Subject Matter Expert writing, reviewing, and approving Informed Consent Forms for clinical trial sites• Continued role as the Sponsor main point of contact for site study and regulatory coordinators and Principal Investigators, and study vendors and CROs

Indianapolis, Indiana, Us

- Informed Consent Form Subject Matter Expert- Study Start-Up Subject Matter Expert- Electronic Trial Master File (eTMF) implementation and Subject Matter Expert- Reviewing and approving site monitoring visit reports- Coordinating regulatory document collection - Creating and submitting study-level IRB submissions - Reviewing and processing site invoices for payment- Maintaining site regulatory documents and trial master files

Indianapolis, Indiana, Us

- Reviewed site regulatory documents during study start-up and during trial - Created and maintained study and site-level trial master files- Informed Consent Form Subject Matter Expert- Created and shipped site regulatory binders- Maintained open lines of communication with sites during trial

Indianapolis, Indiana, Us

- Reviewed and maintained site and trial master files- Created and shipped site regulatory binders- Assisted Clinical Research Associates and Clinical Trial Managers with site correspondences and maintenance

Hockessin, Delaware, Us

• Choreographed pieces to be performed at competitions and correcting dancers’ technique and mistakes• Coached dancers to become disciplined while having fun and instilling a strong work ethic • Travelled with dance teams to competitions, conventions, and other special performances

Columbia, Maryland, Us

• Coordinated interviews, orientations, and start dates for over 20 employees, increasing the amount billed to one client from $1,600/week to over $35,000/week over the course of seven months• Supervised, trained and mentored four other recruiters in the office to increase business production• Recruited healthcare professionals for temporary and permanent employment with hospitals, healthcare facilities, and schools• Developed sound relationships with prospective and active clients to maintain and facilitate staffing opportunities

• Corresponded with patients’ physicians to transfer and/or receive patient care information• Verified patients’ coverage and eligibility with insurance companies and interpreted insurance and treatment information for patients• Scheduled patients’ visits with a team of therapists while coordinating the therapists’ schedules to ensure complete patient care

Wilmington, Delaware, Us

• Welcomed and assisted fans and corporate groups• Monitored fans’ safety and security

• Compiled consent forms in compliance with the Institutional Review Board • Collected and interpreted research data and performed statistical analysis on data spreadsheets

• Conducted virtual reality and Electroencephalography (EEG) tests on the subjects and analyzed results• Informed subjects about the tests that they will be completing during their visit and ensured all subjects were comfortable and all of their questions were answered

Bachelor Of Science - Bs, Honors Kinesiology - Movement Science

Master Of Science - Ms, Biomechanics And Movement Science

Education record