Research Nurse

2 weeks ago

Rockville, United States Cape Fox Shared Services Full time

Concentric Methods is seeking a Registered Research Nurse to join our team in Bethesda, MD in support of the NIH.

Responsibilities:

  • Utilize established resources to design study methods to meet study objectives.
  • Work with staff to coordinate and collect epidemiologic, genetic, and clinical data.
  • Participate in an interdisciplinary team supporting clinical evaluation and follow-up.
  • Provide instruction to potential clinical study subjects and those involved in the care of subjects on aspects of the subject's care, treatments, and side effects.
  • Provide patient education for protocol participants to ensure patient safety and protocol adherence.
  • Monitor and support activities pertaining to clinical protocols, such as monitoring patient recruitment and retention, trial progress, and the need for extension or renewal of ongoing trials.
  • Coordinate various activities to ensure proper filing of serious adverse events, amendments, annual reports, and other regulatory documents.
  • Support the collection, data entry, and assistance with special procedures for patients.
  • Organize and maintain an active referral list and master schedule for planning follow-up and new patient admissions.
  • Collaborate with other members of the team in managing the patient's progress throughout treatment
  • Obtain informed consent/assent as needed.
  • Collaborate with other members of the team for the collection, processing, and handling of research and clinical laboratory samples inside and outside of NIH.
  • Ensure that all aspects of Good Clinical Practice (GCP) are met or exceeded.
  • Complete all source documentation and Case Report Form.
  • Maintain thorough and organized study documentation, including research records, phone logs, screening logs, regulatory binders, and accurate drug accountability records.
  • Provide expertise in patient care coordination and implementation of protocol requirements during onsite visits.
  • Work with staff on the preparation and implementation of study protocols.
  • Recruit and evaluate clinical study subjects, scheduling appointments, and interviews.
  • Prepare IRB documentation, including initial submissions, protocol amendments, protocol modifications, Adverse Event Reports, protocol deviations, protocol violations, continuing review, and informed consent documents.

Cape Fox Corporation, its subsidiaries, and affiliates provide equal employment opportunities to all persons and prohibit employment decisions on the basis of race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation. Cape Fox Corporation, its subsidiaries, and affiliates offer preference to Cape Fox Corporation shareholders, descendants, and other Native Americans pursuant to Public Law 100-241.

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