Heart Rhythm Clinical Research Solutions

This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Program Coordinator

Program ManagerProgram ManagerFull TimeRemote

Location

United States

Posted

47 days ago

Salary

Not specified

No structured requirement data.

Job Description

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more.

Role Description

The Program Coordinator – Scientific Affairs supports the planning, coordination, and execution of HRCRS scientific initiatives, serving as a central operational and research support role within the Scientific Affairs department. This position blends project coordination, research assistance, and scientific operations, enabling the successful delivery of registry-based research, survey research projects, investigator collaborations, and sponsor-supported studies.

  • Coordinate timelines, milestones, and deliverables for Scientific Affairs projects, including registry studies, survey research initiatives, and collaborative research programs
  • Track project status, action items, and dependencies to ensure timely execution and follow-through
  • Support meeting preparation, documentation, and follow-up for scientific working groups, investigator meetings, and research workshops
  • Assist with research protocol development, study documentation, and regulatory or ethics-related materials as needed
  • Support data-related activities, including data cleaning support, literature reviews, qualitative transcript organization, or synthesis preparation
  • Assist in the preparation of scientific outputs such as abstracts, posters, reports, and internal research summaries
  • Maintain organized study files and documentation in accordance with HRCRS research standards
  • Serve as a liaison between Scientific Affairs and internal teams such as Operations and RWE
  • Coordinate with external stakeholders, including clinicians, investigators, research sites, and industry partners
  • Support collaborative research activities by organizing inputs, tracking feedback, and synthesizing outputs
  • Maintain accurate project documentation, trackers, and reporting tools to support transparency and accountability
  • Prepare internal status updates and summary materials for Scientific Affairs team
  • Contribute to continuous improvement of Scientific Affairs workflows, templates, and project management practices
  • Stay current with developments in clinical research, public health research, and implementation science
  • Support special projects and emerging initiatives within the Scientific Affairs department as assigned

Qualifications

  • Bachelor’s or Master’s degree in a scientific field such as Public Health, Health Sciences, Epidemiology, Biology, Social Sciences, or a related discipline
  • A combination of relevant education and substantial experience in clinical, public health, or health services research
  • Prior experience or formal training in research methods (quantitative, qualitative, or mixed methods)
  • Experience in a research, academic, healthcare, CRO, or public health setting preferred
  • Strong organizational and project coordination skills, with the ability to manage multiple workstreams simultaneously
  • Working knowledge of research workflows, including protocol development, data collection, IRB-related processes, or study documentation
  • Excellent written and verbal communication skills, particularly for scientific and professional audiences
  • High attention to detail and commitment to accuracy in documentation and reporting
  • Proficiency with collaborative tools and project tracking platforms (e.g., MS Teams, MS Excel, HubSpot)
  • Ability to work independently while contributing effectively to cross-functional scientific teams
  • Interest in real-world evidence, implementation science, healthcare innovation, or medical technology evaluation

Requirements

  • This is a fully remote position and may be performed anywhere within the United States of America
  • Occasional domestic travel may be required for company meetings, audits, etc.
  • This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Job Requirements

  • Bachelor’s or Master’s degree in a scientific field such as Public Health, Health Sciences, Epidemiology, Biology, Social Sciences, or a related discipline
  • A combination of relevant education and substantial experience in clinical, public health, or health services research
  • Prior experience or formal training in research methods (quantitative, qualitative, or mixed methods)
  • Experience in a research, academic, healthcare, CRO, or public health setting preferred
  • Strong organizational and project coordination skills, with the ability to manage multiple workstreams simultaneously
  • Working knowledge of research workflows, including protocol development, data collection, IRB-related processes, or study documentation
  • Excellent written and verbal communication skills, particularly for scientific and professional audiences
  • High attention to detail and commitment to accuracy in documentation and reporting
  • Proficiency with collaborative tools and project tracking platforms (e.g., MS Teams, MS Excel, HubSpot)
  • Ability to work independently while contributing effectively to cross-functional scientific teams
  • Interest in real-world evidence, implementation science, healthcare innovation, or medical technology evaluation
  • This is a fully remote position and may be performed anywhere within the United States of America
  • Occasional domestic travel may be required for company meetings, audits, etc.
  • This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

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