Summary
Overview
Work History
Education
Skills
Certification
Languages
Timeline
Generic

Credo Mutabaruka

Westvalley,Utah

Summary

Analytical, organized, and detail-oriented Clinical Research Early Phase Manager with a collaborative team-player mentality and a track record of delivering strategic solutions to resolve challenges and drive business growth through employee development.

Extensive knowledge of Good Clinical Practice (GCP) and International Council for Harmonization (ICH) guidelines. Proven experience in coordinating with study teams, follow-up coordinators, dosing departments, and quality assurance units to ensure seamless clinical trial execution. Demonstrated ability to identify operational inefficiencies and implement strategies that enhance productivity and compliance.

Overview

10
10
years of professional experience
1
1
Certification

Work History

Screening Department Manager ,Early Phase Clinical

ICON PLC,
10.2023 - Current

Experience

Screening department Manager ,Early Phase Clinical Services

ICON PLC, Millcreek, Utah | October 2023 – Present

  • Managed a team of 14 direct reports, overseeing daily screening operations and patient scheduling to meet study objectives and enrollment targets.
  • Reduced staff turnover significantly through effective mentoring, regular 1:1 meetings, and professional development initiatives.


  • Increased screening numbers from screening 250 volunteers/ week to 400 volunteers / week creating a 40% increase in enrollment without additional staffing by streamlining scheduling and operational workflows and contributing to the most profitable year in ICON SLC history.
  • Developed quality control tools and training programs that consistently exceeded internal and regulatory quality standards.
  • Successfully implemented new e-source documentation (Clin-Spark system) training, resulting in improved data accuracy and streamlined processes across departments.
  • Collaborated closely with study teams and business development to optimize site operations and develop innovative recruitment strategies.
  • Oversee patient enrollment, scheduling, screening, and data collection processes to meet study objectives.
  • Collaborate with cross-functional teams to optimize trial operations and address challenges proactively.
  • Developed comprehensive training materials and conducted onboarding sessions for new team members, including Administrative Assistants and Clinical Research Coordinators, ensuring robust understanding of medical history all study assessments collection, protocols breakdown and quality standards.
  • Created and implemented quality control checks, consistently exceeding departmental and regulatory quality benchmarks.
  • Streamlined efficient screening process and supported the screening department in daily operations, scheduling, and patient activity management, directly contributing to efficient subject screening and data management.
  • Assisted in data entry, query resolution, and maintenance of source documentation in compliance with clinical trial regulations.
  • Worked in tandem with study team members and quality assurance personnel to facilitate smooth site qualification, initiation, monitoring, and close-out activities.
  • Provided training and operational support to ensure proper handling of laboratory specimens, informed consent processes, and adherence to study protocols.

Senior Medical Research Associate

​ICON PLC​ (formerly PRA Health Sciences)
07.2021 - 10.2023
  • Mentored junior team members, providing guidance and support to enhance their professional development.
  • Served as shift lead, managing clinic floor operations in the absence of the screening manager.
  • Organized study startup activities on the screening floor, ensuring efficient and compliant processes.
  • Explained consent processes and screened potential volunteers, maintaining high ethical standards.

Medical Research Associate

​ICON (formerly PRA Health Sciences)
09.2019 - 07.2021
  • Screened potential subjects and performed basic medical procedures, including informed consent, vital signs, phlebotomy, ECGs, and specimen collection.
  • Ensured all study activities were completed on schedule and in compliance with protocols, FDA, and IRB requirements.
  • Assisted with study setup, check-in/check-out activities, and interacted with clients as appropriate.
  • Monitored subject safety and reported equipment malfunctions, contributing to a safe clinical environment.

Laboratory Associate

​Intermountain Healthcare
09.2017 - 09.2019
  • Performed sample collection procedures, including venipuncture, capillary puncture, blood cultures, and throat/nasal swabs.
  • Properly identified patients and labeled samples, ensuring accuracy and integrity.
  • Instructed patients and family members on sample collection procedures, enhancing the patient experience.
  • Identified opportunities for process improvement and executed projects to enhance operational efficiency.

Case Manager

Asian Association of Utah
01.2015 - 09.2017

· Helped create proposals for funding.

· Worked with sponsors and donors to help them better understand our mission and how we can impact the community.

  • Organized fundraisers.
  • Worked with diverse groups and educated on our mission and vision statement.
  • Worked with team members to create awareness.

· Developed appropriate care plans for at-risk individuals and high-risk families.

· Coordinated resources from diverse providers for intervention plans.

· Coordinated support services and optimized communication between healthcare workers and patients.

· Communicated with legal services providers, social services agencies and local judicial systems regarding cases.

· Worked in close relationship with my clients building trust which helped in the execution of better services.

Education

Associate of Arts - Business Administration And Management

Salt Lake Community College
Salt Lake City, UT
05-2026

Skills

  • Team leadership
  • Team Development
  • Project management
  • Cross-Functional Collaboration
  • Quality Assurance & Regulatory Compliance
  • Scheduling & Workforce Management
    Data Entry & Source Documentation

  • Proficient in E- source ( Clin-spark) documantation, SharePoint, Microsoft Office Suite, and CTMS
  • Patient and clinical procedures

Certification

Certifications

  • Phlebotomist Certification, Oquirrh Mountain
  • Good Clinical Practice (GCP) Certification, CITI
  • Human Investigational Procedures (HIPS) Certification, CITI
  • Columbia-Suicide Severity Rating Scale (C-SSRS) Certification, RFMH
  • Cambridge Assessment of Thinking Skills (CANTAB)

Languages

French
Native or Bilingual
Swahili
Native or Bilingual

Timeline

Screening Department Manager ,Early Phase Clinical

ICON PLC,
10.2023 - Current

Senior Medical Research Associate

​ICON PLC​ (formerly PRA Health Sciences)
07.2021 - 10.2023

Medical Research Associate

​ICON (formerly PRA Health Sciences)
09.2019 - 07.2021

Laboratory Associate

​Intermountain Healthcare
09.2017 - 09.2019

Case Manager

Asian Association of Utah
01.2015 - 09.2017

Associate of Arts - Business Administration And Management

Salt Lake Community College
Credo Mutabaruka