Zemmie Pollock Email & Phone Number

Albuquerque, New Mexico

Albuquerque, New Mexico, United States

• Managed Studies for Radiation Oncology Dept at Rust & Kaseman Hospitals• Demonstrated proficiency with RedCap, EPIC, Mosiaq, IntelliTRIAL, Microsoft Office Suite• Understanding of GCP and HIPPA • Reviewed & QC’d data for audits and responded to audit reports.• Developed familiarity with IRB Procedures Protocol (coordinating with auditors for compliance) Updated personnel on training requirements.  Generating yearly reports and audits• Managed multiple aspects of studies including: Coordinating w/ different depts for study milestones Training coworkers on study procedures Screening prospective patients Education of patients about study and requirements Obtained informed consents, time-point data, study samples. Training coworkers on study procedures Screening prospective patients Education of patients about study and requirements Obtained informed consents, time-point data, study samples. Data management Scheduled Patient Follow-ups• Worked with Compliance for: Protocol modifications Addition of personal to the study DOA log Study deviations and violations• Finalizing study for final report and publication• Working with MD Anderson for study activities• Worked with MDA IRB, MDA Legal, PHS Legal and PHS IRB to transition studies when MDA announced that they were not renewing contact with PHS.

Albuquerque, New Mexico, United States

• Managed Studies for Radiation Oncology Dept at Rust & Kaseman Hospitals• Demonstrated proficiency with RedCap, EPIC, Mosiaq, IntelliTRIAL, Microsoft Office Suite• Understanding of GCP and HIPPA • Reviewed & QC’d data for audits and responded to audit reports.• Developed familiarity with IRB Procedures Protocol (coordinating with auditors for compliance) Updated personnel on training requirements.  Generating yearly reports and audits• Managed multiple aspects of studies including: Coordinating w/ different depts for study milestones Training coworkers on study procedures Screening prospective patients Education of patients about study and requirements Obtained informed consents, time-point data, study samples. Training coworkers on study procedures Screening prospective patients Education of patients about study and requirements Obtained informed consents, time-point data, study samples. Data management Scheduled Patient Follow-ups• Worked with Compliance for: Protocol modifications Addition of personal to the study DOA log Study deviations and violations• Finalizing study for final report and publication• Working with MD Anderson for study activities• Worked with MDA IRB, MDA Legal, PHS Legal and PHS IRB to transition studies when MDA announced that they were not renewing contact with PHS.

Albuquerque, New Mexico Area

• Designed and implemented business marketing plans.• Proficient with SalesForce• Prospecting for new clients• Coordinated Child ID Events• Managed client files with multiple agencies• Interviewed individuals, families and business owners concerning their protection needs and financial goals.• Presented strategies to resolve financial concerns.

Albuquerque, New Mexico Area

• Demonstrated proficiency with Microsoft Office Suite, Share Point• Prepared numerous proposals for submission to sponsors.• Authored Study Protocols• Developed familiarity with IACUC procedures including: Protocols (coordinating with auditors for compliance) Generating yearly usage reports and ordering animals• Reviewed and QC’d data for audits and responded to audit reports.• Authored and reviewed Standard Operating Procedures (SOPs)• Authored interim and final reports• Data Management• Prepared studies for FDA submittal• Worked with USDA, CDC, FDA• Coordinated with collaborators on multiple continents.• Completed numerous DOJ and DOD Clearances• Project Management of Studies including but not limited to: Coordinating with different departments for timelines on study milestones Training and supervising technicians on study procedures Working with Vendors for training and equipment, software repairs and upgrades Ordering supplies and equipment Reviewing resumes and interviewing potential new hires On-Boarding and Mentoring new hires Evaluation of clinical symptoms Collaborating with different departments Reviewed and monitored study budgets for accurate billing and meeting study financial goals.• Coordinated GLP and non-GLP studies for multiple areas. ABSL1-3 and BSL2-3 Toxicology, Pharmacology, Cell Therapy, Telemetry, Cardiovascular Various Government Agencies and Pharmaceutical Companies• Worked with multiple Agents and Diseases including: HPAI, Seasonal and Swine flu, Monkey Pox, Anthrax, SARS, MERS Hantavirus, Tularemia, VEE/EEE, Botulism, Rabies Pulmonary Arterial Hypertension (PAH)• Received vaccinations for Anthrax, Vaccinia, Rabies• Performed Aerosol Exposures: Nose-only, Head-only, Whole body.• Supervised all telemetry including: Set-up and ran validation scripts. Set-up programs for data collection, processing data Proficient with different Telemetry software (EMKA, CARecorder, ITS, DSI, VRR)