Medical Study Coordinator

1 day ago


Rockville, Maryland, United States Cape Fox Shared Services Full time

Key Responsibilities

The Research Nurse Specialist will be responsible for coordinating and conducting clinical studies, ensuring the highest level of patient care and data quality. Key responsibilities include:

  • Design and implement study protocols: Utilize established resources to design study protocols that meet study objectives, working with staff to coordinate and collect epidemiologic, genetic, and clinical data.
  • Conduct patient education: Provide instruction to potential clinical study subjects and those involved in their care on aspects of their treatment and side effects.
  • Maintain study documentation: Ensure all aspects of Good Clinical Practice (GCP) are met or exceeded, completing source documentation and Case Report Forms.
  • Collaborate with teams: Collaborate with other members of the team to manage patient progress throughout treatment, obtain informed consent/assent as needed, and ensure accurate drug accountability records.
  • Recruit and evaluate subjects: Schedule appointments, interviews, and prepare IRB documentation, including initial submissions, protocol amendments, and Adverse Event Reports.

About the Company

Cape Fox Shared Services is committed to providing equal employment opportunities to all persons and prohibits employment decisions based on race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation. We offer preference to Cape Fox Corporation shareholders, descendants, and other Native Americans pursuant to Public Law 100-241.



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