UT Health - San Antonio, TX

posted 6 months ago

Full-time - Mid Level
San Antonio, TX
Educational Services

About the position

The Research Scientist position at UT Health Science Center at San Antonio involves a multifaceted role that encompasses the planning, designing, monitoring, coordinating, analyzing, and producing of scientific content specifically tailored for clinical and regulatory documents. This position is critical in ensuring that all scientific documentation meets the necessary standards and requirements for clinical research and regulatory submissions. The successful candidate will be responsible for managing and reviewing the medical writing associated with study protocols, statistical analyses, and study reports, ensuring accuracy and compliance with regulatory guidelines. In this role, the Research Scientist will collaborate closely with various stakeholders, including clinical researchers, statisticians, and regulatory affairs professionals, to develop comprehensive and clear documentation that effectively communicates research findings and methodologies. The position requires a strong understanding of clinical research processes and the ability to translate complex scientific information into accessible formats for diverse audiences. Additionally, the Research Scientist will be expected to stay abreast of the latest developments in clinical research and regulatory requirements, contributing to the continuous improvement of documentation practices within the organization. This role is essential for supporting the integrity and credibility of research conducted at UT Health Science Center, ultimately contributing to advancements in medical science and patient care.

Responsibilities

  • Plan and design scientific content for clinical and regulatory documents.
  • Monitor and coordinate the production of scientific documentation.
  • Analyze data and produce reports for clinical studies.
  • Manage and review medical writing for study protocols and statistical analyses.
  • Ensure compliance with regulatory guidelines in all documentation.
  • Collaborate with clinical researchers and statisticians to develop clear and comprehensive documentation.

Requirements

  • PhD in a relevant scientific field or equivalent experience.
  • Strong background in clinical research and regulatory documentation.
  • Proven experience in medical writing and scientific communication.
  • Excellent analytical and organizational skills.
  • Ability to work collaboratively in a multidisciplinary team environment.

Nice-to-haves

  • Experience with statistical analysis software.
  • Familiarity with Good Clinical Practice (GCP) guidelines.
  • Previous experience in a research-intensive environment.

Benefits

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