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Network Power<100 people
Roles
💸100%
Marketing
✨100%
Business Owner
🖋️100%
Copywriting
Geos
Work Background
Baylor Scott & White Health Temple TxCST
Feb. 2025Temple, Texas, United States
Aya HealthcareTravel Scrub Tech
Jan. 2024 - Feb. 2025United States
Baylor Scott & White HealthCertified Surgical Technologist
Jan. 2022 - Jan. 2024Temple, Texas, United States
University Medical Center Of LubbockCertified Surgical Technologist
Jul. 2019 - Jan. 2022Lubbock, Texas Area
TAC AirCustomer Service Representative
Jul. 2018 - Jan. 2019Amarillo, Texas
Brownwood Iron and MetalOffice Assistant
May. 2016 - Jan. 2018Brownwood, Texas
Michael R MacAdams, M.D.Clinical Research Coordinator
Jun. 2011 - Oct. 2011Diabetes Clinical Research
VA North Texas HospitalResearch Coordinator
Sep. 2009 - Apr. 2010Perform regulatory activities related to submission to IRBs and sponsors for approval. Knowledgeable of protocols so that all study activities are performed correctly and completely. Design and maintain organizational tools to monitor conduct and progress of a study accurately in compliance with GCP. Query resolution from sponsors and IRBs. Obtain proper written informed consent from each study subject prior to participation in the study. Review of patient medical records. Maintain all records of the study including receipt, dispensing and return off all clinical supplies and to respond to all discrepancies. Communicates with PI and sponsor regarding study activities. Screen potential study subjects according to study I/E criteria.
2006 - 2007 Amarillo Heart Group Clinical Research InstituteClinical Research Clinical Research Coordinator
Feb. 2006 - Jan. 2007Schering Plough CRA Responsible for conducting clinical research and cleaning up a clinical trial. Responsible for assuring the integrity of this institution by following the trial regulations through the local IRB and ICH/GCP guidelines. Conducted site visit everyday until study site was cleaned and the study was closed. Worked along side Shering Plough CRA. 2002; Responsible for numerous clinical trials, patient recruitment, pharmaceutical contact, patient care and appropriate patient follow-ups, source documentation and posting, CFR posting, laboratory technician and abnormality follow-ups, regulatory documentation and reporting AE and SAE events.
AAMR Research ClinicDirector
Jan. 2005 - Mar. 2009In the last four years I have: Perform regulatory activities related to submission to IRBs and sponsors
for approval. Knowledgeable of protocols so that all study activities are performed correctly and
completely. Design and maintain organizational tools to monitor conduct and progress of a study
accurately in compliance with GCP. Query resolution from sponsors and IRBs. Obtain proper written
informed consent from each study subject prior to participation in the study. Review of patient medical
records. Maintain all records of the study including receipt, dispensing and return off all clinical
supplies and to respond to all discrepancies. Maintain required documentation in study file and
patient's medical records. Maintain records of study subject's status in the study. Made sure site had
source documents if none were provided by sponsor company. Ensure safety and welfare of study
subjects. Communicates with PI and sponsor regarding study activities. Approves and maintains
appropriate SOPs for the research site. (Procedures based on GCP and FDA guidelines.) Performs
annual training for research department staff. Assist with recruitment. Screen potential study subjects
according to study I/E criteria including: recruit new clinical studies and oversee clinical conduct of
investigational studies according to FDA regulations and guidelines. Conduct daily meetings with
study staff and investigators on study related progress. Specialties
grants, budgets, contracts
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