Summary
Overview
Work History
Education
Skills
Trials
Publications
Certifications
References
Timeline
Generic

Hassan Rizk

Dearborn Heights,USA

Summary

Dedicated clinical research professional with extensive experience as a clinical research coordinator. Proven adeptness in adhering to study protocols, standard operating procedures, and good clinical practices, ensuring rigorous compliance throughout all phases of research projects. Known for strong problem-solving skills and meticulous attention to detail, facilitating smooth operations and accurate documentation.

Overview

9
9
years of professional experience

Work History

Clinical Study Coordinator

Henry Ford Health
06.2024 - Current
  • Gastroenterology and Hepatology
  • Participated in planning meetings with sponsors and CROs to discuss objectives of upcoming studies
  • Discussed research study with potential research participants
  • Reviewed participants' medical records to track and report adverse events and deviations
  • Developed comprehensive knowledge of ICH-GCP and FDA regulations to ensure compliance with study protocols
  • Created and maintained clinical trial documentation, including case report forms, informed consent forms and regulatory documents
  • Identified potential issues that could impact the successful completion of a study according to protocol requirements
  • Ensured that all relevant regulatory documents were collected from investigative sites before initiating any study activities
  • Collaborated with research team members to develop strategies for collecting patient data from medical charts or electronic health records
  • Developed effective working relationships with investigative sites, sponsors and CROs, IRBs, vendors and other stakeholders involved in clinical studies
  • Collected and recorded accurate and complete data, including medical histories, laboratory results, and adverse events, in accordance with study protocols and regulatory guidelines
  • Conducted informed consent discussions with study participants, ensuring their understanding of study procedures, risks, and benefits
  • Scheduled subjects for appointments, procedures, and inpatient stays as required by study protocols
  • Assessed eligibility of potential subjects through methods such as screening interviews, reviews of medical records and discussions with physicians and nurses
  • Directed requisition, collection, labeling, storage, or shipment of specimens
  • Communicated with laboratories and investigators regarding laboratory findings
  • TRACER studies
  • ONCORE and EPIC utilization


Clinical Research Coordinator

Revive Research Institute, Inc.
12.2020 - 08.2022
  • Coordinated data collection and assist in protocol amendments
  • Screen and enroll subjects in all clinical trials
  • Worked alongside clinical Principal Investigators, sponsors, and institutions to support, facilitate, and coordinate daily clinical trial activities
  • Maintain a working knowledge of all federal regulation and good clinical practices as related to clinical research and ensuring all studies are in compliance with federal regulations and policies
  • Coordinated and completes case report forms
  • Scheduling and conducting all study follow-ups
  • Performing EKG's
  • Coordinated all related monitor visits
  • Coordinated Phase I II III COVID Plasma Antibody trials
  • Developed and maintained clinical trial documents, such as protocols, case report forms, and informed consent forms
  • Organized and conducted investigator meetings to ensure protocol compliance
  • Reviewed patient charts for accuracy prior to data entry into the database
  • Managed drug supply inventory for multiple trials
  • Monitored laboratory results to ensure quality control of data collected
  • Conducted training sessions for research staff on Good Clinical Practices
  • Collaborated with project managers to identify potential issues that could affect the timeline of a study
  • Tracked adverse events reports from participating sites throughout the course of each trial
  • Ensured appropriate documentation was completed by investigators in accordance with ICH and GCP guidelines
  • Prepared monthly progress reports outlining key milestones achieved during the month
  • Maintained accurate records of all correspondence related to clinical trial activities
  • Provided support in preparation for FDA inspections including review of relevant documents
  • Kept patient care protocols and clinical trial operations in compliance
  • Mentored and provided ongoing support to research team, providing training in research design and conduct
  • Adhered to standards in areas involving data collection, research protocols and regulatory reporting
  • Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants
  • Collected, processed and delivered specimens from trial participants
  • Educated participants on studies and anticipated outcomes
  • Placed orders for medications to be used in studies
  • Monitored subject enrollment and tracked dropout details
  • Risk mitigation and issue resolution- proactively identifies and mitigates risks
  • Resolves and documents issues in real-time
  • Conducted screening interviews to determine eligibility of possible subjects

COVID-19 Mobile Testing

Wayne State University School of Medicine
03.2020 - 01.2021
  • Multiple roles for testing first responders and civilians within metro Detroit
  • Phlebotomist: Draw 1 to 4 tubes for serology and biobanking
  • Registration: Print labels and submit lab orders
  • Confirm that the number of samples collected have orders created
  • Lab Technician: Centrifuge blood samples and properly store equipment
  • Quality Assurance: Confirm all information on lab request form is correct
  • Ensure the label on the tube matches the paper form

Clinical Research Coordinator

Wayne State University School of Medicine
09.2016 - 01.2021
  • Coordinated community Blood Pressure health events such as May Measurement Month, working at farmer's markets, local churches, and working closely with the American Heart Association and all of their community events
  • Collected community blood pressures using REDCap and OnCore systems
  • Analyzed data to use in future grant submissions
  • Coordinated Hypertension-related studies
  • Built database using REDCap for data collection
  • Coordinated data collection and assist in protocol amendments
  • Screened and enrolled subjects in all Emergency Medicine conducted clinical trials
  • Worked alongside clinical Principal Investigators, sponsors, and institutions to support, facilitate, and coordinate daily clinical trial activities and provide guidance on the administration of the compliance, financial, personnel and other related aspects of clinical studies
  • Maintained a working knowledge of all federal regulation and good clinical practices as related to clinical research and ensuring all studies are in compliance with federal regulations and university policies
  • Collected documents and maintains data to assist investigators in implementing research protocols and remaining on target timelines
  • Coordinated and completes case report forms
  • Scheduling and conducting all study follow-ups
  • Performing EKG's
  • Screening and testing patients for HIV/HCV diseases
  • Coordinated all related monitor visits
  • Site coordinator at Sinai Grace Hospital where I assisted in managing a team where we tested for HIV and linking HIV positive patients to care
  • Coordinated HIV testing day from 2016-2019
  • Worked with Michigan Department of Health and Human Services in regards to linking patients to care and plugging in HIV numbers as well as positive results each month

Project Assistant

Sinai Grace Hospital
05.2015 - 09.2016
  • Assistant for grant funded programs housed in the emergency department
  • Trained incoming staff in technical skills (venipuncture, EKG's, etc.) and sample processing
  • Site coordinator at Sinai Grace Hospital where I assisted in managing a team where we tested for HIV and Hepatitis C in the Emergency Department

Education

BSN -

Wayne State University
12.2026

Public Health -

Wayne State University
12.2019

Skills

  • Protocol Adherence
  • Good Clinical Practices (GCP)
  • Regulatory Compliance
  • Data Collection and Management
  • Case Report Form Completion
  • Patient Screening and Enrollment
  • Study Follow-up Procedures
  • Drug Supply Inventory Management
  • Training and Mentoring
  • Problem-solving
  • Attention to Detail
  • Time Management
  • Team Collaboration
  • Communication (both written and verbal)
  • EKG Administration
  • Patient Education
  • Risk Management
  • Phlebotomy
  • EPIC
  • ONCORE
  • TRACER Studies
  • Site monitoring
  • Informed Consent Process

Trials

  • Enrolled in the SHINE trial (Stroke Hyperglycemia Insulin Network Effort), in which we assess whether tight glucose control in stroke patients accounts for a good neurological outcome. It is a Phase III multi-centered, randomized, controlled trial.
  • Enrolled in the POINT trial (Platelet-Oriented Inhibition in New TIA and minor ischemic stroke), in which we assess whether aspirin and Plavix will prevent the recurrence of a stroke after a TIA. It is a randomized, double-blind, multi􏰀centered clinical trial.
  • Enrolled in the RELAX-AHF Trial which was "A multi-center, randomized, double-blind, placebo-controlled phase IIIb study to evaluate the efficacy, safety and tolerability of SERELAXIN when added to standard therapy in Acute Heart Failure Patients"
  • Enrolled patients in the ICON-RELOADED trial (International Collaborative of NT-proBNP re-evaluation of acute diagnostic cut-offs in the emergency department), in which we assess the etiology of shortness of breath by measuring various levels of biomarkers released during an acute episode.
  • Enrolled in VALIDATION OF POINT-OF-CARE TBI DETECTION SYSTEM FOR HEAD INJURED PATIENTS (B- AHEAD III Trial) Enrolled in A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SARS-CoV-2 Neutralizing Antibody BGB-DXP593 in Patients With Mild to Moderate COVID-19
  • Enrolled in J2W-MC-PYAB a Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of LY3819253 and LY3832479 in Patients With Mild to Moderate COVID-19 illness
  • Enrolled in J2W-MC-PYAH a Randomized, Double-Blind, Placebo-Controlled Phase 2 Study to Evaluate the Efficacy and Safety of Mono and combination Therapy and Monoclonal Antibody in participants with Mild to Moderate COVID- 19 illness (BLAZE-4)
  • Enrolled in CTAP101-CL-2014 A Randomized, Double-Blind Placebo-Controlled Study to Evaluate the Safety and Efficacy of Rayaldee (calcifediol) Extended-release Capsules to Treat Symptomatic Patients Infected with SARS-CoV- 2 (REsCue)
  • Coordinated the National institutes of Health (NIH) – ACTIV-2/A5401
  • Coordinated Partner Therapeutics, Inc. – PTX-001-003
  • Coordinated ALRN-6924-1-03 A Phase 1b/2 Study of the Dual MDMX/MDM2 Inhibitor, ALRN-6924, for the Prevention of Chemotherapy-induced Myelosuppression
  • Coordinated A Randomized, Prospective, Multi-center Trial to Assess the Efficacy of a Cryotherapy Device Versus Best Supportive Oral Care in Mitigating Symptoms of Oral Mucositis in Patients Receiving Chemotherapy for the Treatment of Cancer
  • Suzhou Connect Biopharmaceuticals Ltd. - CBP-201-WW002 / 256558, A Multi-center, Randomized, Double-blind, Parallel Group, Placebo-controlled, Efficacy and Safety Study of CBP-201 in Patients with Moderate to Severe Persistent Asthma with Type 2 Inflammation
  • Genentech, Inc. - GB43311, A Phase IIb, Randomized, Double-blind, Placebo-Controlled, Multicenter study to evaluate the efficacy and safety of Astegolimab in patients with chronic obstructive pulmonary disease.
  • Sanofi- A Randomized, Double-Blind, Placebo controlled Study Assessing the Long-term Effect of Dupilumab on Prevention of Lung Function Decline in Patients with Uncontrolled Moderate to Severe Asthma
  • A Phase 2, Double-blind, Randomized, Placebo-controlled, Parallel-group, Study to Evaluate the Efficacy and Safety of LX9211 in the Treatment of Patients with Postherpetic Neuralgia (RELIEF-PHN1) LX9211.1-202-PHN

Publications

1. Katee Dawood, BS, Bethany Foster, MPH, Jonathon Ottolini, Daniel Foley, Hassan Rizk, Maxwell Wheaton, Revelle Gappy, & Phillip Levy, MD, MPH. May Measurement in Detroit- A Global Campaign to Raise Awareness for Blood Pressure Control.

2. Dawood K, Foster B, Ottolini J, Foley D, Rizk H, Wheaton M, Gappy R, Levy P. May Measurement Month in Detroit􏰀A global campaign to raise awareness for blood pressure control. 2018 Global Health and Innovation Conference; New Haven, CT. April 2018

Certifications

BLS Certification, ACLS Certification, Michigan certified HIV Test Counselor, Human Subjects Research - Biomedical Investigators, Human Subjects Research - Social & Behavioral Researchers, CITI Good Clinical Practice Course, 09/03/2023, CITI Health Information Privacy and Security (HIPS), Responsible Conduct of Research - Social and Behavioral , CITI Conflicts of Interest - 03/28/2024, Environmental Health & Safety Biological Substances , Shipping and Transport of Regulated Biological Materials

References

Val Mika, Wayne State University, vmika@med.wayne.edu
Katee Dawood, Wayne State University, kdawood@wayne.edu

Timeline

Clinical Study Coordinator

Henry Ford Health
06.2024 - Current

Clinical Research Coordinator

Revive Research Institute, Inc.
12.2020 - 08.2022

COVID-19 Mobile Testing

Wayne State University School of Medicine
03.2020 - 01.2021

Clinical Research Coordinator

Wayne State University School of Medicine
09.2016 - 01.2021

Project Assistant

Sinai Grace Hospital
05.2015 - 09.2016

BSN -

Wayne State University

Public Health -

Wayne State University
Hassan Rizk