Summary
Overview
Work History
Education
Skills
Certification
Projects
Timeline
Generic

Ariam Tedla

Woodbridge

Summary

Dynamic Clinical Research Coordinator at Medstar Health Research Institute with expertise in regulatory compliance and trial coordination. Proven track record in enhancing participant retention and improving recruitment rates through innovative outreach strategies. Strong leadership and data integrity skills drive successful clinical trial outcomes while ensuring adherence to GCP and FDA regulations.

Overview

7
7
years of professional experience
1
1
Certification

Work History

Clinical Research Coordinator

Medstar Health Research Institute
Washington
11.2023 - Current
  • Recruited and enrolled eligible participants, obtained informed consent, and ensured compliance with study protocols
  • Maintained regulatory compliance and documentation, including the preparation and submission of reports to institutional review boards (IRBs) and regulatory agencies.
  • Monitored participant progress, managed adverse events, and reported deviations from protocol to relevant stakeholders
  • Coordinated with various departments and personnel to ensure smooth study operations and effective communication
  • Prepared and submitted regulatory documentation, including IRB submissions and communications with regulatory bodies
  • Oversaw the inventory of study supplies and medications.
  • Provide training and mentorship to staff on research protocols, SOPs, and best practices in clinical research and data handling.
  • Conduct routine data reviews and integrity checks to ensure accurate and timely reporting of clinical trial data.
  • Lead and oversee day-to-day operations for multiple clinical trials, ensuring compliance with GCP, FDA regulations, and internal study protocols.
  • Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
  • Increased participant retention rates through proactive follow-up efforts and regular engagement activities.
  • Conducted thorough literature reviews supporting the development of innovative study designs and methodologies.
  • Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
  • Contributed to the successful completion of clinical trials by proactively resolving issues, mitigating risks, and meeting deadlines in a fast-paced environment.
  • Improved recruitment rates by developing and implementing effective patient outreach strategies.
  • Managed study budgets and resources to maximize return on investment while maintaining quality standards.
  • Enhanced patient compliance with study protocols by creating informative and engaging participant materials.
  • Improved trial visibility and public interest through effective community outreach and education initiatives.
  • Facilitated successful trial completion by closely monitoring study timelines and milestones, ensuring on-time delivery of results.
  • Implemented electronic data capture system, significantly reducing paper use and increasing data retrieval efficiency.

STD/HIV Surveillance Liason

Virginia Dept. of Health
01.2022 - 10.2023
  • Coordinated and managed STD/HIV surveillance activities, including data collection, analysis, and reporting
  • Developed and maintained relationships with local health departments, clinics, and community organizations to enhance surveillance efforts
  • Conducted outreach and education programs to raise awareness about STD/HIV prevention and testing
  • Analyzed surveillance data to identify trends, emerging issues, and high-risk populations, and provided actionable insights to stakeholders
  • Prepared and presented detailed reports on STD/HIV prevalence, incidence, and trends to inform public health strategies and policy decisions
  • Ensured compliance with federal, state, and local health regulations and guidelines related to STD/HIV surveillance
  • Collaborated with epidemiologists, public health officials, and researchers to support and implement surveillance projects and initiatives
  • Managed and updated surveillance databases, ensuring data accuracy, confidentiality, and security
  • Coordinated with healthcare providers to facilitate the reporting and follow-up of STD/HIV cases
  • Provided training and technical support to staff and partners on surveillance procedures, data entry, and reporting protocols
  • Conducted QA audits of surveillance protocols and database entries, identifying areas for process improvement and corrective action.
  • Collaborated closely with department heads to identify opportunities for process improvement initiatives.
  • Improved interdepartmental collaboration with regular team building activities and open forums for discussion.
  • Managed complex schedules to coordinate travel, meetings, and events for executive leadership teams.

Patient Access Team Lead

Inova Health Systems
01.2018 - 01.2022
  • Supervised and mentored a team of patient access specialists, ensuring effective performance and adherence to departmental policies and procedures
  • Managed patient intake and registration processes, including verifying insurance coverage, obtaining necessary authorizations, and ensuring accurate data entry
  • Coordinated scheduling of patient appointments and procedures, optimizing clinic flow and resource utilization
  • Handled complex patient inquiries and resolved issues related to insurance coverage, billing, and access to care
  • Developed and implemented training programs for new hires, focusing on best practices in patient access, customer service, and compliance
  • Monitored team performance metrics and conducted regular evaluations to ensure high standards of service and operational efficiency
  • Collaborated with healthcare providers, insurance companies, and other departments to facilitate smooth patient interactions and streamline workflows
  • Oversaw the management of patient financial assistance programs, including identifying eligible patients and assisting with application processes
  • Conducted audits and quality checks on patient access activities to ensure accuracy and compliance with regulations and internal policies
  • Prepared and presented reports on team performance, patient access metrics, and operational improvements to senior management
  • Acted as a liaison between patients, healthcare providers, and Medicaid agencies to facilitate clear communication and resolve issues
  • Prepared and analyzed reports on patient access metrics, Medicaid enrollments, and team performance to support decision-making and strategic planning
  • Provided exceptional customer service, addressing patient inquiries, concerns, and complaints related to Medicaid coverage and access
  • Stayed updated on changes in Medicaid policies and regulations, ensuring the team's knowledge and practices remained current

Education

Doctor of Health Science (D.H.Sc.) -

Purdue University
11.2025

Master of Science (M.S.) - Healthcare Administration

Radford University
05.2022

Bachelor of Arts (B.A.) - Biology and Psychology

Radford University
12.2017

Skills

  • Clinical QA & Compliance: GCP, GMP, FDA/ICH regulations, IRB submissions, quality audits, protocol compliance
  • Data Integrity & Reporting: Data validation, analysis, risk management, adverse event reporting, audit reporting
  • CAPA Management: Root cause analysis, corrective/preventive action plans, audit findings resolution
  • Trial coordination: Full lifecycle clinical trial management, recruitment, data management, and site coordination
  • Regulatory Documentation & Reporting: Clinical trial documentation, regulatory filings, study progress reports, regulatory agency communications
  • Medical Terminology & Terminology Understanding: Strong understanding of clinical and pharmaceutical terminology
  • Leadership & Staff Training: Supervision, mentoring, training development, performance evaluations
  • Risk Management: Risk assessments, process optimization, compliance management, auditing best practices

Certification

  • CME
  • CEU

Projects

Perinatal Depression Brief Psychological Intervention in Obstetrics

End-User Research in Support of Long-Acting Injectable Multiple Prevention Technology, Discrete Choice Experiment

Materna Prep Clinical Trial

Preterm Birth Reduction Initiative: Maternal Health Quality Improvement

Timeline

Clinical Research Coordinator

Medstar Health Research Institute
11.2023 - Current

STD/HIV Surveillance Liason

Virginia Dept. of Health
01.2022 - 10.2023

Patient Access Team Lead

Inova Health Systems
01.2018 - 01.2022

Doctor of Health Science (D.H.Sc.) -

Purdue University

Master of Science (M.S.) - Healthcare Administration

Radford University

Bachelor of Arts (B.A.) - Biology and Psychology

Radford University
Ariam Tedla