Houston Methodist - Houston, TX

posted 2 months ago

Full-time - Mid Level
Houston, TX
501-1,000 employees
Nursing and Residential Care Facilities

About the position

The Research Program Manager at Houston Methodist Academic Institute is responsible for coordinating processes that align the research and clinical interests of faculty and physicians with affiliated institutions. This role serves as a liaison for ongoing program activities, facilitating collaboration between research and clinical investigators, and managing relationships with industry partners. The position involves strategic planning, resource allocation, and maintaining organized documentation to support projects from pre-clinical to clinical stages.

Responsibilities

  • Coordinate face-to-face discussions between collaborators to encourage effective idea transfer.
  • Develop and maintain positive working relationships with collaborators, ensuring timely updates on project modifications.
  • Serve as a liaison between multiple client groups and stakeholders across various management levels.
  • Communicate results clearly and provide organized progress reports.
  • Assist in the preparation and coordination of business development materials and activities for the program.
  • Support outreach, pilot programs, and project management activities for major projects and grants.
  • Write SOPs and other regulatory documentation as needed.
  • Maintain organized records of collaborative projects and participants for reporting purposes.
  • Coordinate elements required for translating pre-clinical safety studies in support of medical devices.
  • Manage project-relevant information and documentation from conception to completion.

Requirements

  • Bachelor's degree required; Master's or terminal degree preferred.
  • Three years of experience in a health center (academic or clinical).
  • Portfolio Management Professional (PMP) certification preferred.
  • Strong communication and presentation skills.
  • Advanced spreadsheet skills, including pivot tables and v-lookups.
  • Strong project and time management skills.

Nice-to-haves

  • Experience in a research or clinical environment.
  • Knowledge of regulatory requirements for clinical studies.

Benefits

  • Health insurance
  • Paid holidays
  • Professional development opportunities
  • Flexible scheduling
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