Clinical Research Coordinator Resume Example
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 [Number] years of related experience to a challenging new role.
Gullas College Of Medicine - City
University Of Illinois At Chicago - City, State
- Member of Activities Honor Society
- Minored in Chemistry
University Of Miami Miller School Of Medicine – Miami , FL
- Study Areas: Rheumatology, Cardiology, Dermatology, Endocrinology, and General Medicine
- Phase II-IV Studies
- 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.
- Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Followed informed consent processes and maintained records.
- Performed duties in accordance with all applicable standards, policies and regulatory guidelines to promote safe working environment.
- Used critical thinking to break down problems, evaluate solutions and make decisions.
- Created plans and communicated deadlines to ensure projects were completed on time.
- Worked closely with CRO, Sponsors, CRA to maintain optimum levels of communication to effectively and efficiently complete projects.
- Informs IRB of serious adverse events, assists in completing enrollment logs
- Processes regulatory documents
- Maintains/organizes Trial master file/Investigator Site file
Weis Memorial Hospital – City , STATE
- Promoted office efficiency, coordinating charts, completing insurance forms and helping patients with diverse needs.
- Enhanced patient outcomes by providing knowledgeable education on procedures, medications and other physician instructions.
- Assisted with routine checks and diagnostic testing by collecting and processing specimens.
- Prepared and administered medications to alleviate patient symptoms.
- Collected and documented patient medical information such as blood pressure and weight.
- Directed patients to exam rooms, fielded questions and prepared for physician examinations.
- Coordinated with appropriate administrative staff to address clinical, operational and financial questions.
- Taught patients about medications, procedures and care plan instructions.
- Documented vital signs and health history for patients
- Participated in all scheduled rounds and teaching conferences.
- Collected data on patients, including labs and test results.
- Observed and recorded patient conditions by assessing vitals.
- Assisted patient medication administrations using various methods such as intravenous, intramuscular, oral, subcutaneous and pulmonary.
- Reviewed medical testing requests to determine validity of diagnostic testing requests.
- Provided medical care and treatment in Level-2 Trauma Unit for patients
- Met with patients to discuss medical histories and current complaints.
- Diagnosed and treated patients suffering from chronic conditions including diabetes, hypertension and dyslipidemia.
- Recorded patients' health histories and provided over 50 consultations weekly.
- Diagnosed issues and implemented treatment plans to resolve problems or help manage symptoms.
- Leveraged expertise to assist patients in addressing routine infections as well as more complex concerns facing specific populations.
- Implemented therapeutic regiments involving medications and other interventions to mitigate symptoms and prevent reoccurrence.
- Devised treatment plans for disorders involving cardiovascular, endocrine and other internal systems.
- Conducted physical assessments of relevant body areas and performed standardized tests to check responses.
Larkin Community Hospital – City , STATE
- Worked in Internal Medicine departments to gain hands-on experience.
- Participated in all scheduled rounds and teaching conferences.
- Collected data on patients, including labs and test results.
- Observed and recorded patient conditions by assessing vitals.
- Assisted patient medication administrations using various methods such as intravenous, intramuscular, oral, subcutaneous and pulmonary.
- Reviewed medical testing requests to determine validity of diagnostic testing requests.
- Administered specialized treatment for multiple patients daily.
- Met with patients to discuss medical histories and current complaints.
- Recorded patients' health histories and provided consultations daily
- Diagnosed issues and implemented treatment plans to resolve problems or help manage symptoms.
- Teamed with other physicians, specialists and health care providers to provide well-rounded care for complex cases.
- Reviewed patient files and records, including allergies, problems, medications and immunization statuses.
- Leveraged expertise to assist patients in addressing routine infections as well as more complex concerns facing specific populations.
- Conducted physical assessments of relevant body areas and performed standardized tests to check responses.
- Devised treatment plans for disorders involving cardiovascular, endocrine and other internal systems.
Hhh – City , STATE
Joanna Figueroa “Elevated Liver Enzymes in Asymptomatics”
Department of Internal Medicine
Weis Memorial Hospital
Joanna Figueroa “Hepatitis B Serology”
Department of Internal Medicine Morning Rounds
Larkin Community Hospital
Joanna Figueroa “CNS Demyelinating and Inflammatory Disease”
Department of Neurology
Chong Hua Hospital
Joanna Figueroa “HIV Prophylaxis Management”
Department of Family Medicine Morning Rounds
Chong Hua Hospital
Joanna Figueroa “A Case of Terminal Dysuria”
Department of Internal Medicine Grand Rounds
Chong Hua Hospital
Joanna Figueroa “Persistent Left Superior Vena Cava”
Department of Pediatrics Grand Rounds
John H. Stroger Hospital
Joanna Figueroa “Preventative Health Care for Women”
Educational Class for Women
Gullas Health Community Center
“Stress Levels of First Year to Third Year Regular Students of Gullas College of Medicine”
Department of Pharmacology and Therapeutics
Gullas College of Medicine
“The Effectivity of Moringa oliefera extract on inhibition of Methicillin Resistant Staphylococcus Aureus in Comparison to Vancomycin”
Departement of Pharmacology
Cebu Institute of Medicine
1. Biohaven Pharmaceuticals, Inc.
“BHV3500-202: A phase 2/3 Open-label, Long-Term, Safety Trial of BHV-3500 (zavegepant) intranasal (IN) for the Acute Treatment of Migraine”
Study Coordinator
2. AbbVie, Inc.
“A Phase 3 Randomized, Placebo-Controlled, Double-Blind Study to Evaluate Upadacitinib in Adolescent and Adult Subjects with Moderate to Severe Atopic Dermatitis”
Study Coordinator
3. AbbVie, Inc.
“Testosterone Replacement therapy for Assessment of long-term Vascular Events and efficacy ResponSE in hypogonadal men (TRAVERSE) Study”
Study Coordinator
4. Abbvie Inc.
“A Randomized, Active-Controlled, Efficacy Assessor-Blinded Study to Evaluate Pharmacokinetics, Safety and Efficacy of Risankizumab in Patients from 6 to Less than 18 Years of Age with Moderate to Severe Plaque Psoriasis”
Study Coordinator
5. Biohaven Pharmaceuticals, Inc.
“A Phase 2/3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Rimegepant in Migraine Prevention
Study Coordinator
6. Eli Lilly and Company
“The Effect of Tirzepatide versus Dulaglutide on Major Adverse Cardiovascular Events in Patients with Type 2 Diabetes (SURPASS-CVOT)”
Study Coordinator
7. Esperion Therapeutics, Inc
“A Randomized, Double-blind, Placebo-controlled Study to Assess the Effects of Bempedoic Acid (ETC-1002) on the Occurrence of Major Cardiovascular Events in Patients with, or at high risk for, Cardiovascular Disease who are Statin Intolerant”
Study Coordinator
8. Kowa Research Institute, Inc.
“Pemafibrate to Reduce cardiovascular OutcoMes by reducing triglycerides IN patiENts with diabeTes (PROMINENT)”
Study Coordinator
9. Novo Nordisk
“SELECT - Semaglutide effects on cardiovascular outcomes in people with overweight or obesity”
Study Coordinator
9. Novo Nordisk
10. Novo Nordisk
“Semaglutide cardiovascular outcomes trial in patients with type 2 diabetes (SOUL)”
Study Coordinator
11. Tonix Pharmaceuticals, Inc.
“A Phase 3, Double-Blind, Randomized, Multicenter, Placebo-Controlled Study to Evaluate the Efficacy and Safety of TNX-102 SL Taken Daily At Bedtime In Patients with Fibromyalgia, "RELIEF Study”
Study Coordinator
12. Dyve Biosciences
“Randomized, double-blinded, placebo-controlled study of the efficacy and safety of DYV700 for reducing pain associated with an acute gout flare”
Study Coordinator
13. Samumed, LLC
“A Phase 3, 28-Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of SM04690 Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects”
Study Coordinator
14. Samumed, LLC
“A Phase 3, 56-Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Utilizing Patient-Reported and Radiographic Outcomes to Evaluate the Efficacy and Safety of a Single Injection of SM04690 Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
Study Coordinator
15. GlaxoSmithKline Research & Development Limited
“A 24-week, phase 3, multicentre, randomised, double-blind, efficacy and safety study, comparing GSK3196165 with placebo and with sarilumab, in combination with conventional synthetic DMARDs, in participants with moderately to severely active rheumatoid arthritis who have an inadequate response to biological DMARDs and/or Janus Kinase inhibitors”
Study Coordinator
16. GlaxoSmithKline Research & Development Limited
“A multi-centre long-term extension study to assess the safety and efficacy of GSK3196165 in the treatment of rheumatoid arthritis.”
Study Coordinator
17. AOBiome Therapeutics
“A Phase II, Randomized, Double-Blind, Vehicle Controlled Study of the Efficacy, Safety, and Tolerability of B244 Topical Spray for the Treatment of Pruritus in Adults with a History of Atopic Dermatitis”
Study Coordinator
18. DS Biopharma
“A Randomised, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of Orally Administered DS107 in Adult Patients with Moderate to Severe Atopic Dermatitis”
Study Coordinator
19. Quantum Genomics
“A Phase 3, Double-blind, Placebo-controlled, Efficacy and Safety Study of Firibastat (QGC001) Administered Orally, Twice Daily, Over 12 Weeks in Difficult-to-treat/Resistant Hypertensive Subject”
Study Coordinator
20. Concert Pharmaceuticals
“A Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy and Safety of CTP-543 in Adult Patients with Moderate to Severe Alopecia Areata”
Study Coordinator
21. Amgen
“A Phase 2 Dose Ranging Study to Evaluate the Efficacy and Safety of AMG 570 in Subjects With Active Systemic Lupus Erythematosus (SLE) With Inadequate Response to Standard of Care (SOC) Therapy”
Study Coordinator
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Resume Overview
School Attended
- Gullas College Of Medicine
- University Of Illinois At Chicago
Job Titles Held:
- Clinical Research Coordinator
- Hands-On Clinical Extern
- Post Graduate Sub Intern
- Medical Student Surgery
Degrees
- M.D. : Doctor of Medicine , 2016
Bachelor of Science : Biological Sciences , 2011
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