Chantelle Sanchez
Cicero,IL
Summary
Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Certified in GCP, IPS, Human Research and Medidata Classic RAVE.
Overview
3
3
years of professional experience
1
1
Certification
Work History
Research Study Coordinator
Northwestern University
11.2023 - Current
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Gathered, shipped, and entered data on lab specimens.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Followed informed consent processes and maintained records.
- Managed patient recruitment, informed consent process and data entry to support trial objectives.
- Monitored patient safety throughout clinical trials and reported any adverse events.
- Followed research protocols and conducted study visits in compliance with IPS,GCP and Human Research regulations.
- Submitted budget tracking and payment for each patient and healthy volunteer.
Research Assistant
Northwestern University
11.2021 - 10.2023
- Analysis and collection of data as well as creating and populating REDCap database.
- Weekly participation in research meetings pertaining to projects assigned to me.
- Instructions are received from principal investigators in weekly meetings on their data analysis needs, output needs, and provide status updates of previous data analysis.
- Recruiting, evaluating eligibility, scheduling and consenting participants into research studies.
- Updating Study Tracker and filing patient forms.
Research Intern
Northwestern University
09.2021 - 11.2021
- Completing and assisting with data collection and analysis
- Participation in weekly research meetings pertaining to projects assigned to me
- Instructions are received from principal investigators in weekly meetings on their data analysis needs, output needs, and provide status updates of previous data analysis
- A variety of research-related tasks are assigned and completed on an ad-hoc basis.
Education
Bachelor of Arts - Biochemistry
DePauw University
Greencastle, Indiana05.2021
Skills
- Data Collection and Design
- Informed consent
- Clinical Research
- Patient recruitment
- Participant screening
- Good Clinical Practices
- Research SOPs understanding
- Study protocols
- Experienced in R coding
- Experienced in Excel
Certification
- Biomedical Research certificate
- Good Clinical Practice certificate
- HIPAA, Security and Privacy certificate
- Medidata Classic RAVE EDC Essentials for Clinical Research Coordinators
- RAVE EDC: Bayer- Safety Dataflow
- Brainshark Protocol Training certificate
Activities
- DePauw First, First Generation Organization- DePauw University, 02/2018-05/2021, President, Handling and organizing events and activities geared to first generation students., Leading members through meetings and accomplishing pending tasks.
- DePauw First, First Generation Organization- DePauw University, 08/2019-05/2021, Treasurer, Calculating and managing budgets for different events and activities., Contacting other organizations or businesses for collaborations or orders.
- Committee for Latinx Concerns Organization- DePauw University, 08/2019-12/2020, Treasurer, Calculating and managing budgets for different events and activities., Contacting other organizations or businesses for collaborations or orders.
Languages
Spanish
Native or Bilingual
Chinese (Mandarin)
Elementary
Korean
Elementary
Timeline
Research Study Coordinator
Northwestern University
11.2023 - Current
Research Assistant
Northwestern University
11.2021 - 10.2023
Research Intern
Northwestern University
09.2021 - 11.2021
Bachelor of Arts - Biochemistry
DePauw University
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