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Georgetown Universityposted about 2 months ago
$21 - $35/Yr
Full-time • Entry Level
Hybrid • Washington, DC
Educational Services

About the position

Georgetown University Medical Center seeks to provide excellence in education and cutting-edge interdisciplinary research collaboration to improve human health. The Clinical Research Coordinator 2 (CRC2) is responsible for managing and coordinating the ALL ALS studies, primarily in the disease states of Neuromuscular Disorders (ALS). This role requires refined technical, organization, interpersonal, and coordination skills. The CRC2 will conduct study visits, maintain patient confidentiality, oversee regulatory maintenance, and coordinate with various departments. The position requires spending 5 days per week on-site and interacting with other coordinators across the country.

Responsibilities

  • Conduct the entire study visit for each patient, ensuring that the protocol is followed.
  • Maintain a comprehensive functional knowledge of ancillary departments involved in trial visits.
  • Perform job maintaining patient confidentiality at all times.
  • Oversee regulatory maintenance and accurate reporting of clinical trial visits.
  • Coordinate the ALL ALS studies at the Georgetown University Hospital Dept. of Neurology and with remote patients.
  • Interact with other coordinators around the country and follow a central IRB protocol.

Requirements

  • Bachelor's degree; exceptions may be made for an Associate's Degree with 5 years minimum work experience as a Clinical Trial Coordinator or Clinical Research Assistant.
  • At least 3 years of experience working in a clinical setting with direct patient interaction.
  • Minimum 2 years of experience as a Clinical Trial Coordinator, Clinical Research Assistant, or equivalent position.
  • Experience working with Neurology patients, specifically in MS and neuromuscular clinics.
  • Previous experience with regulatory maintenance, preparation, and IRB submission activities.
  • Current CITI Group 1 Biomedical, HIPAA, and IATA Training.
  • Experience handling human biological specimens and operating a centrifuge.
  • Ability to access and read patient medical records and knowledge of medical care/operations.
  • Highly detail-oriented, organized, and able to work respectfully in a team.
  • Excellent communication skills with respect to external and internal communication.

Benefits

  • Medical insurance
  • Dental insurance
  • Vision insurance
  • Disability insurance
  • Life insurance
  • Retirement savings
  • Tuition assistance
  • Work-life balance benefits
  • Employee discounts
  • Voluntary insurance options

Job Keywords

Hard Skills
  • B
  • C
  • Clinical Research
  • Clinical Trials
  • Operations Research
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Soft Skills
  • ONbrlGVFa5 U4ygWuI85qb
  • RraXEs7 Akwnz4oSK
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