Clinical Research Scientist, Regulatory & Medical Writing

A major health institution in San Antonio is seeking a qualified candidate for a role focused on planning, designing, and coordinating scientific content for clinical and regulatory documents. Responsibilities include executing complex research projects and collaborating in developing innovative research methodologies. Candidates must hold a Master's degree and have at least two years of related experience. Knowledge of specific software tools and effective communication skills are paramount.

A comprehensive benefits package, including medical, dental, and time off, is offered.
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