CITLALI VELAZQUEZ GARCIA
Huntington Park,CA
Summary
Dedicated Clinical Research Coordinator experienced in complying with study protocols, standard operating procedures and good clinical practices. A research professional proficient in handling patient information, laboratory samples and compliance procedures for diverse clinical trials. Highly organized with excellent communication and planning skills
Overview
5
5
years of professional experience
1
1
Certification
Work History
Clinical Research Coordinator
Amicis Research Center
Northdrige, California
12.2023 - Current
- Performed patient assessments, collected and analyzed data, and prepared reports.
- Coordinated investigator meetings, conference calls, and site initiation visits as needed.
- Communicated effectively with investigators, study staff, sponsors, vendors, IRB personnel, and other stakeholders throughout the life cycle of the trial.
- Maintained accurate up-to-date tracking logs for all aspects of clinical research activities including but not limited to adverse events, serious adverse events, concomitant medications, lab results .
- Kept patient care protocols and clinical trial operations in compliance.
- Collected, processed and delivered specimens from trial participants.
- Took vital signs and collected medical histories as part of study protocols.
- Conducted screening interviews to determine eligibility of possible subjects.
- Educated participants on studies and anticipated outcomes.
Clinical Research Coordinator
Pasadena Clinical Trials
Pasadena, CA
10.2023 - 11.2023
- Help Site Manager create and file documents in regulatory binders.
- Performed patient assessments, collected and analyzed data, and prepared reports.
- Took vital signs and collected medical histories as part of study protocols.
- Vaguely trained in unblinded procedures
Clinical Research Assistant
Century Research Institute
Huntington Park, CA
11.2022 - 08.2023
- Conducted screening visits for new participants, explained and went over thoroughly the ICF before participants signed
- Administer vaccines to qualified participants after signing the ICF
- Scheduled on site visits for participants within the visit window and scheduled monthly phone calls for participants as well
- Completed study case forms for participants and file sources in participants charts
- Documented and entered data in EDC using the imedidata program
- Revised and organized charts before monitor visits.
Customer Service Associate
Dulfi Fiesta Candy
Huntington Park, CA
07.2019 - 11.2022
- Accepted cash and credit card payments
- Tracked outgoing orders to provide shipping status to customers
- Received incoming product deliveries and relocated to storage shelves, coolers and warehouse
- Updated products with new pricing or temporary promotions to increase sales.
Education
Medical Assistant Diploma -
UEI College
12.2022
High School Diploma -
Huntington Park Senior High
06.2018
Skills
- Data Analysis
- Phlebotomy
- Specimens Collection and Processing
- Patient Scheduling
- Data Entry
- Electrocardiography (EKG)
- Vital Signs Documentation
- Patient Registration
- Critical Thinking
- Well Organized
- Great computer skills
Clinical Research Experience
Bavarian Nordic
A Randomized, Double-Blind, Phase 3 Trial to Assess Clinical Efficacy, Safety and Reactogenicity of the Recombinant MVA-BN-RSV Vaccine in Adults ≥60 years of Age
Sanofi US Services Inc.
Safety and Immunogenicity of Quadrivalent Influenza mRNA Vaccine MRT5410 in Adults Aged 18 Years and Older
UCB Biopharma SRL
A PHASE 1/2A, RANDOMIZED,PLACEBO-CONTROLLED, SINGLE-ASCENDING DOSE(PART A,PARTICIPANT-AND INVESTIGATOR-BLIND) AND REPEAT-DOSE (PART B, PARTICIPANT-,INVESTIGATOR-, AND SPONSOR-BLIND) STUDY TOINVESTIGATE THE SAFETY, PHARMACOKINETICS,AND EFFICACY (PART B ONLY) OF UCB1381 INHEALTHY STUDY PARTICIPANTS (PART A) AND INSTUDY PARTICIPANTS WITH MODERATE TOSEVERE ATOPIC DERMATITIS (PART B)
Highlightll
A randomized, double-blinded, placebo-controlled, multicenter Phase 2 study evaluating the efficacy and safety of TLL018 in participants with moderate-to-severe plaque psoriasis
Cara Therapuetics
A 2 part, Multicenter, Randomize, Double-blind Study to Evaluate the Efficacy and Safety of Oral Difelikefalin for Moderate-to-Sever Pruritus in Adults Subjects with Notalgia Paresthetica
AstraZeneca
A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Parallel-Group, Dose-Ranging Study to Evaluate CIN-107 for the Treatment of Patients With Uncontrolled Hypertension and Chronic Kidney Disease
Ionis Pharmaceuticals Inc.
A Randomized, Double-Blind, Placebo- Controlled, Phase 3 Study of Olezarsen (ISIS 678354) in Patients with Hypertriglyceridemia and Atherosclerotic Cardiovascular Disease (Established or at Increased Risk for), or with Severe Hypertriglyceridemia
Languages
English
Native/ Bilingual
Spanish
Native/ Bilingual
Certification
- Handling of Category A, Infectious Substance Affecting Humans- Mayo Clinic Laboratories
- Good Clinical Practice- NIDA Clinical Trials Network
EDC and IRT Systems
- Medidata Rave
- Suvoda
- Clario
- 4G Clinical
- Endpoint
- Long Boat
References
References available upon request.
Timeline
Clinical Research Coordinator
Amicis Research Center
12.2023 - Current
Clinical Research Coordinator
Pasadena Clinical Trials
10.2023 - 11.2023
Clinical Research Assistant
Century Research Institute
11.2022 - 08.2023
Customer Service Associate
Dulfi Fiesta Candy
07.2019 - 11.2022
Medical Assistant Diploma -
UEI College
High School Diploma -
Huntington Park Senior High
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