Full-Time

Senior Research Project Manager

Women's Health

Posted on 11/30/2025

University of Texas at Austin

University of Texas at Austin

No salary listed

Company Does Not Provide H1B Sponsorship

Austin, TX, USA

In Person

Category
Business & Strategy (1)
Requirements
  • Bachelor’s degree with five (5) years’ relevant clinical research experience, project administration/coordination, or Masters degree and three years related experience.
  • Previous experience with subject recruitment and retention, and data management, and management experience within a large organization.
  • Demonstrated ability to discuss personal topics with patients in a compassionate, sensitive manner.
  • Demonstrated detail orientation, ability to follow-through, and strong problem-solving skills.
  • Must possess effective project management skills, including the ability to plan, organize and schedule work in an efficient and productive manner, focusing on key priorities and meeting deadlines.
  • Ability to work independently and on a team. Excellent written, oral, and interpersonal communication skills.
  • Proficiency in Microsoft Excel, Word, and PowerPoint and willingness to learn other technologies as necessary.
  • Relevant education and experience may be substituted as appropriate.
Responsibilities
  • Work under the guidance of the Director and principal investigators to meet research study objectives.
  • Support day-to-day project management and coordination for multiple studies, which may vary in scope and clinical area.
  • Support the research team to ensure that all study activities are completed according to applicable regulations and guidelines and adhere to the protocol and Good Clinical Practice.
  • Develop and oversee execution of recruitment strategies to ensure recruitment goals are met.
  • Develop, organize, and maintain study databases and ensure data is complete and accurate.
  • Help to facilitate project collaborations and teamwork.
  • Maintain broad organizational perspective to effectively carry out internal and external relationships of the program.
  • Oversee the collection and maintenance of appropriate source documentation and ensure accurate entry into study specific databases.
  • Manage, document, and report on adverse events, compliance, and other participant related safety issues.
  • Collaborate with investigators to ensure proper conduct of all aspects of clinical research.
  • Implement and recommend policies and procedures to ensure compliance of all applicable laws, University policies, rules and regulations.
  • Develop instructional materials to aid new physician investigators with study development and start-up requirements.
  • Oversee the creation and maintenance of research protocols on the clinicaltrials.gov website.
  • Assist with development of QI projects for hospital medicine.
  • Screen, recruit, and enroll eligible patients and track participation over time.
  • Conduct and manage study visits and participant assessments/interviews, which may include collection of biological specimens.
  • Act as primary contact for study participants.
  • Participate in data collection, data entry, and data organization.
  • Manage the consent of participants and completing study visits with participants.
  • Perform Quality Assurance/Quality Control of study data.
Desired Qualifications
  • Bilingual in English and Spanish.
  • Experience working with REDCap, SmartSheet, Qualtrics, and other clinical trial Electronic Data Capture systems.
  • Experience assisting with grant submissions and administration of funds with sponsors such as National Institutes of Health, National Science Foundation, Patient-Centered Outcomes Research Institute, etc.
  • Experience conducting research in University of Texas at Austin Dell Medical School setting, Ascension Seton setting and/or Community Care setting.
University of Texas at Austin

University of Texas at Austin

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