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Emmes Group

CRO services and AI-driven trial infrastructure

Clinical Project Coordinator

Project ManagementUpdated on Nov 10
Full-timeRockville, MD, USANo salary listed

About the Job

Requirements

  • A bachelor's degree is required.
  • Four to six years of relevant project or administrative support experience is required.
  • Demonstrated experience with the Microsoft Office Suite, particularly Microsoft Word, is required.
  • Familiarity and experience with software such as project scheduling, bibliography management, teleconferencing and web conferencing, or website management are valued.
  • Time management and decision-making skills are required.
  • Attention to detail and the ability to handle several assignments simultaneously are required.

Responsibilities

  • Support Emmes project teams with logistics, including conference calls, meetings, supplies, documentation, and client or sponsor reporting needs as required by the statement of work; the role may support Public Sector and BioPharma work.
  • Track project deadlines and compile and submit project deliverables.
  • Schedule and distribute conference call information and materials, including agendas, minutes, and supporting documents.
  • Prepare nontechnical meeting minutes.
  • Coordinate conference calls and remote or in-person meetings, including meetings with international sites and collaborators.
  • Assist with communications between project staff and project sponsors as needed.
  • Manage logistics for inventory and supply management for research sites.
  • Support the development, composition, consolidation, compilation, editing, formatting, tracking, and distribution of reports—including DSMB and scientific committee reports—nontechnical reports, numbered memos, progress reports, site visit reports, project marketing materials, case report forms, study plans, presentations, and manuscripts, following eCTD and/or Section 508 compliance guidelines as required and under the direction of the Clinical Project Coordinator Manager or designee.
  • Maintain systems used to track project rosters, meeting materials, team training records, and other project deliverables.
  • Participate in establishing and maintaining project procedures and processes, such as standard operating procedures and work instructions.
  • Manage electronic project files and archives under the direction of the Clinical Project Coordinator Manager or designee.
  • Maintain project website content and user access under the direction of the Clinical Project Coordinator Manager or designee.
  • Assist with quality reviews based on standards, standard operating procedures, and Good Clinical Practice guidelines, and contribute to department standardization efforts when applicable.
  • Track project publications and manuscripts and support manuscript submission under the direction of the Clinical Project Coordinator Manager or designee.
  • Perform other duties as assigned.
  • Comply with all policies and standards.

About the Company

Emmes Group

CRO services and AI-driven trial infrastructure

Emmes Group combines a contract research organization (CRO) with an AI arm to support clinical research globally. The CRO Emmes provides study design, patient recruitment, data collection, statistics, and regulatory support, while Veridix AI builds software tools to plan, manage, and analyze trials using artificial intelligence. It differentiates itself by offering both hands-on trial services and an integrated AI-powered platform, backed by a long history dating to 1977 and a global health focus. Its goal is to modernize clinical research to make trials faster, safer, and more accessible for patients around the world.

Company size
11-50
Company stage
Not listed
Total funding
Not listed
Headquarters
Rockville, MD
Founded
2024

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