Summary
Overview
Work History
Education
Skills
Study Experience
Timeline
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MURPHY TUREK

Oconomowoc,WI

Summary

Senior Clinical Research Associate with a Master's in Biomedical Sciences, and extensive experience leading complex global clinical trials across oncology, vaccines, infectious disease, immunology, neurology, and rare disease. Recognized as an outstanding performer for exceptional quality, leadership, and operational excellence. Demonstrated ability to manage high-volume study portfolios, maintain top-tier compliance metrics, mentor clinical teams, support cross-functional operations, and drive successful study execution across dynamic research environments.

Overview

10
10
years of professional experience

Work History

Senior Clinical Research Associate

ICON PLC / Pfizer (On Assignment)
Milwaukee, WI
10.2023 - Current
  • Led monitoring activities across global studies, ensuring adherence to ICHGCP and regulatory standards.
  • Maintained exceptional performance metrics with 100% compliance in documentation and training.
  • Recognized for leadership and operational efficiency through multiple performance-based awards.
  • Supported site teams with strategic guidance on enrollment and compliance matters.
  • Mentored junior CRAs by providing co-monitoring and technical training.
  • Selected for high-priority assignments due to proven expertise and reliability.
  • Achieved top-tier operational benchmarks, including 100% trip-report compliance and timely issue resolution.
  • Completed over 75 visits annually, demonstrating commitment to operational excellence.

Clinical Research Associate I/II

ICON PLC
Milwaukee, WI
11.2021 - 10.2023
  • Executed qualification, initiation, monitoring, and close-out visits for global multi-site trials.
  • Performed source data review to ensure accuracy and adherence to protocols.
  • Managed inventory of investigational products, ensuring compliance with storage and reconciliation requirements.
  • Maintained inspection-ready documentation through regular updates of trial master files.
  • Identified protocol deviations and collaborated with site teams to enhance compliance.
  • Directed site audit preparations and efforts for regulatory inspection readiness.

Clinical Research Associate

Barrow Neurological Institute (Medasource)
Phoenix, AZ
04.2021 - 11.2021
  • Managed all site management and trial administration as defined by monitoring plan.
  • Facilitated study startup, ongoing training, site initiation visits, and remote monitoring.
  • Evaluated clinical data and regulatory documents to ensure compliance with study protocol.
  • Prepared timely monitoring reports and coordinated deliverables requests.
  • Collaborated with study team and operations management to enhance project success.
  • Contributed to program development initiatives, improving quality of clinical monitoring services.
  • Executed internal quality control processes for monitoring activities to enhance procedures.
  • Conducted investigational product inventory, reconciliation, and security assessments.

Clinical Research Associate / Jump Team Coordinator

IQVIA (Aerotek)
Scottsdale, AZ
12.2020 - 04.2021
  • Maintained current study protocols, case report forms (CRFs), electronic data capture (EDC) systems, and documentation.
  • Planned logistical activities for study procedures in alignment with established protocols.
  • Managed clinical study readiness through meticulous setup, inventory oversight, and equipment troubleshooting.
  • Executed data entry, performed quality checks, and resolved queries to uphold protocol adherence and accuracy.
  • Conducted complex clinical procedures, including vital signs monitoring, phlebotomy, and lab processing.

Clinical Research Coordinator

Synexus Clinical Research
Chandler, AZ
01.2020 - 12.2020
  • Managed study leadership for over 10 trials in cardiology, infectious disease, and vaccines.
  • Provided support for 30+ clinical studies across multiple medical specialties.
  • Executed detailed informed consent and screening procedures.
  • Accurately recorded AE/SAE data to ensure compliance and safety.

Clinical Research Coordinator

HonorHealth
Scottsdale, AZ
07.2019 - 12.2019
  • Recruited and screened patients to ensure appropriate study participation.
  • Coordinated study visits, optimizing scheduling and participant engagement.
  • Ensured regulatory compliance throughout all phases of research.
  • Managed data effectively, maintaining accuracy and confidentiality.
  • Supported Institutional Review Board submissions to facilitate timely approvals.

Emergency Department Medical Scribe

ThedaCare Regional Medical Center
Appleton, WI
06.2016 - 08.2018
  • Documented patient histories and examination findings in real-time during consultations.
  • Assisted physicians with precise charting during patient procedures.
  • Coordinated with nursing staff to ensure seamless flow of patient information.
  • Managed electronic health record entries for emergency department cases efficiently.

Education

Master of Arts - Biomedical Sciences

Midwestern University
Glendale, AZ
05-2019

Bachelor of Science - Biochemistry

St. Norbert College
De Pere, WI
05-2017

Skills

  • Clinical monitoring and site management
  • Oncology and immunology expertise
  • Vaccine development and administration
  • ICH-GCP compliance
  • Risk-based monitoring strategies
  • Data integrity and issue resolution
  • Query management and resolution
  • TMF/ISF reconciliation
  • CRA mentorship and training
  • Operational excellence in clinical trials
  • Metrics management and analysis
  • EDC and EPRO systems proficiency
  • CTMS and IRT knowledge
  • Microsoft Office Suite proficiency
  • RBM platform experience
  • Specialization in infectious disease, neurology, gastroenterology, endocrinology, cardiovascular, dermatology

Study Experience

  • Vaccines: COVID-19 (all phases), Influenza/COVID combo, Pneumococcal, Lyme disease
  • Oncology: Early-phase advanced solid tumors, metastatic disease
  • Dermatology: Atopic dermatitis
  • Gastroenterology: Eosinophilic GI disorders
  • Neurology: ALS multi-regimen platform
  • COVID-19 prophylaxis
  • RSV challenge model
  • NASH / hematology
  • Endocrinology (men's health)
  • Migraine therapy

Timeline

Senior Clinical Research Associate

ICON PLC / Pfizer (On Assignment)
10.2023 - Current

Clinical Research Associate I/II

ICON PLC
11.2021 - 10.2023

Clinical Research Associate

Barrow Neurological Institute (Medasource)
04.2021 - 11.2021

Clinical Research Associate / Jump Team Coordinator

IQVIA (Aerotek)
12.2020 - 04.2021

Clinical Research Coordinator

Synexus Clinical Research
01.2020 - 12.2020

Clinical Research Coordinator

HonorHealth
07.2019 - 12.2019

Emergency Department Medical Scribe

ThedaCare Regional Medical Center
06.2016 - 08.2018

Master of Arts - Biomedical Sciences

Midwestern University

Bachelor of Science - Biochemistry

St. Norbert College