Research Project Manager for Multi-Site Observational COVID-19 Study - Veteran Affairs Seattle Epidemiologic Research and Information Center

LOCATION: Seattle, WA

CLOSING DATE: February 18, 2021

OPPORTUNITY TYPE: Job

JOB #: 16703

POSTED: December 18, 2020

Description:

  Research Project Manager (Health Sciences) for Multi-Site Observational COVID-19 Study

The multi-year study, CSP #2028: Epidemiology, Immunology, and Clinical Characteristics of COVID-19 (EPIC3) within the Veterans Health Administration, gathers longitudinal data on the epidemiology, virology, immunology, and clinical characteristics of SARS-CoV-2 infections and the COVID-19 disease. CSP #2028 is coordinated by the VA CSP Seattle Epidemiologic Research and Information Center (ERIC).

Apply to join our Center to contribute to a high impact, national research study that aims to provide critical insights on how we understand SARS-CoV-2 infections and the COVID-19 disease, how it impacts Veterans specifically, and how to better anticipate and manage future pandemics.

The Seattle ERIC is hiring a full-time Project Manager. Our team at the Seattle ERIC coordinating center provides overall operational support and coordination to the 16 study sites nationwide. Under the direction of the Program Manager, the Project Manager will provide leadership for this multi-site observational study. This position is based in Seattle, WA.

The Research Project Manager will perform the following key duties under the direction of the Study Program Manager.

Key duties:

  • Work closely with Study Co-Chairs and Investigators to advance scientific aims and study objectives
  • Supervise Study Research Coordinators and Research Assistants
  • Serve as the liaison between the Seattle ERIC and site Investigators, site personnel, central laboratory personnel, consultants, and contractors
  • Manage research operational activities for all study sites, including tracking site personnel and managing site staff permissions to study folders and databases
  • Manage and maintain the Study Operations Manual
  • Manage regulatory processes, including completing R&D and IRB documentation and preparing for audits
  • Maintain the study SharePoint sites, manage site permissions, and upload study documentation
  • Design and develop standard operating procedures, databases, and study materials; maintain and troubleshoot tracking infrastructures
  • Virtually train study site personnel on procedures and protocols including participant tracking measures
  • Monitor subject recruitment and data collection activities at all study sites, identify deficiencies, recommend solutions, and take corrective action when required
  • Oversee data management and quality assurance/quality control procedures
  • Ensure compliance with study protocol, including informed consent, safety, and data security requirements
  • Prepare reports, presentations, and data summaries, and organize national meetings

Qualifications:

  • BA/BS or higher degree in a scientific- or health-related field required; Master’s level degree preferred
  • 4-6 years of work experience in clinical, epidemiological, or health services research required; several years of experience managing high visibility research studies/initiatives preferred
  • Successful management experience
  • Experience with customer service, particularly by telephone
  • Self-starter with demonstrated ability to effectively lead and manage complex projects
  • Experience building internal tracking systems that support attention to detail and quality control
  • Ability to understand and clearly communicate complex regulations and procedures
  • Excellent communication and interpersonal skills with the ability to collaborate with a diverse group of people with a wide range of professional backgrounds and expertise
  • Ability to adapt to evolving and competing priorities and timelines
  • Adept in troubleshooting and problem-solving  
  • Proficiency in Microsoft Office programs (e.g., Word, Excel, Outlook) required; experience with Microsoft Access, Microsoft SharePoint and REDCap programs preferred

About our Center, Seattle ERIC, and how it relates to VA Cooperative Studies Program (CSP):

The Department of Veterans Affairs (VA) Cooperative Studies Program (CSP) is a nationally renowned program that produces innovative solutions to Veteran and national healthcare problems through multi-site research studies.

Founded in 1997, the Seattle ERIC is a research center within CSP that works to improve the health and healthcare of Veterans through epidemiologic research. We’re located in Seattle, WA within the VA Puget Sound Health Care System. We are part of the VA CSP, a national VA research group of 12 epidemiology and clinical trial research centers.

Learn more at:

 

 

How to Apply:

Application information:

Candidates must be U.S. citizens. Education and experience will be evaluated by Human Resources to determine if the top candidate meets the criteria for the targeted GS-11 level. The General Schedule (GS) salary table for Seattle can be found on the Office of Personnel Management website at opm.gov.

Please send a cover letter and resume to SeattleCSPEC@va.gov Applications will be accepted until the position is filled; however, materials received by 01/04/21 will be considered first.