Focused Clinical Research Coordinator well-versed in study protocols, standard operating procedures and general trial oversight. Excellent problem-solving abilities with a detail-oriented nature. Ready to bring 3 years of related experience to a challenging new role.
Skills
Good Clinical Practices
Informed consent
Specimen collections
Trial Management
Study Protocols
Research SOPs Understanding
Documentation Requirements
Scheduling
Data Collection
Schedule Coordination
Clinical Research
Microsoft Office
Project Management
Organization and Time management
Computer skills
Planning and Coordination
Verbal and written communication
Work History
04/2020 to CurrentClinical Research CoordinatorCentura Health | Brighton, CO,
Collected data and followed research protocols, operations manuals and case report form requirements.
Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
Maintained compliance with protocols covering patient care and clinical trial operations.
Coordinated clinical trials focused on disorders such as Crohn's Disease and Acute Spinal Injuries.
Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Monitored unit budget to meet financial objectives for spend rate and funding.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Gathered, processed and shipped lab specimens.
Followed informed consent processes and maintained records.
Used critical thinking to break down problems, evaluate solutions and make decisions.
Developed team communications and information for meetings.
11/2019 to CurrentPatient Experience RepresentativeAscension Health | Warren, MI,
Attended to patient and family's immediate needs and concerns by acknowledging and providing required attention.
Organized and replenished unit supplies to maintain team readiness for expected demands.
Supported patient admissions, discharges and transfers to promote team efficiency.
Monitored, tracked and conveyed important patient information to healthcare staff to help optimize treatment planning and care delivery.
Interacted effectively with patients, families, staff and other hospital department staff to deliver high level of customer service and teamwork.
Answered patient assistance calls, assessed needs and offered qualified support.
08/2019 to 04/2020Clinical Research Assistant IIBeaumont Hospitals | Dearborn Heights, MI,
Educated patients regarding all facets of clinical study participation.
Assisted with research protocol development.
Demonstrated advanced knowledge of federal regulatory compliance guidelines.
Collected, evaluated and modeled collected data.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
03/2018 to 08/2019Clinical Research SpecialistDuke University | Durham, NC,
Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Gathered, processed and shipped lab specimens.
Coordinated clinical trials focused on disorders such as Homocysturnia and PKU.
Followed informed consent processes and maintained records.
Collected data and followed research protocols, operations manuals and case report form requirements.
Maintained excellent attendance record, consistently arriving to work on time.
Maintained compliance with protocols covering patient care and clinical trial operations.
Completed all paperwork, recognizing any discrepancies and addressing them in a timely fashion.
Exceeded goals through effective task prioritization and great work ethic.
Developed team communications and information for meetings.
Quickly learned new skills and applied them to daily tasks, improving efficiency and productivity.
Education
Expected in 06/2022Master of Science | Regulatory AffairsNortheastern University, Boston, MAGPA:
Expected in 05/2016Bachelor of Science | PsychologyMillsaps College, Jackson, MSGPA:
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