Clinical Trials Coordinator

2 weeks ago

Washington, United States The George Washington University Full time

Department Overview:

The George Washington University (GW) Cancer Center, established in 2015, is a collaborative initiative involving the George Washington University, GW Hospital, and GW Medical Faculty Associates, aimed at enhancing efforts in cancer research and treatment. Our mission is to work towards a cancer-free future through innovative research, education, and equitable healthcare.

Position Summary:

The Clinical Research Coordinator plays a pivotal role in supporting various research initiatives within a designated Practice Area. This role encompasses essential clinical and administrative tasks, including data management and participant tracking, ensuring compliance with both regulatory and clinical standards. The Coordinator operates independently to facilitate Investigator-Initiated studies and other clinical trials across all phases. Responsibilities include conducting trial activities, analyzing research data, and assisting in the preparation of regulatory submissions, reports, funding proposals, and other necessary documentation.

Key Responsibilities:

  • Evaluate patient eligibility for studies by gathering medical history and health information as dictated by research protocols, while maintaining confidentiality and professionalism.
  • Extract and compile clinical data from medical records.
  • Execute clinical and administrative tasks in accordance with study protocols, such as measuring vital signs, performing venipuncture, and completing case report forms.
  • Monitor participant safety by tracking adverse reactions, documenting findings, and collaborating with the principal investigator.
  • Manage institutional review board documentation, including submissions and ongoing reviews.
  • Oversee recruitment strategies, including referrals and advertising efforts.
  • Coordinate patient appointments and liaise with other departments for necessary testing.
  • Prepare and manage study samples for storage and distribution.
  • Attend investigator meetings and contribute to the development of new research proposals.
  • Perform additional duties as assigned, which may include related tasks not explicitly listed.

Special Requirements:

Proficient in using office equipment such as computers, telephones, and various software applications including Microsoft Office and OnCore.

Qualifications:

Applicants should possess a BA/BS degree along with a minimum of two years of relevant experience. Certification in clinical research is preferred.

Preferred Skills:

  • Certifications such as CRCC, CCRA, or CCRP are advantageous.
  • Strong verbal and written communication skills, along with leadership capabilities.
  • Excellent organizational and problem-solving skills, with a detail-oriented approach.
  • Ability to adapt to changing responsibilities and manage multiple projects effectively.
  • Demonstrated capacity to work collaboratively in a team environment.
  • Willingness to acquire new technical skills as necessary for the role.
  • Ability to communicate effectively with a diverse range of stakeholders.

Compensation and Benefits:

The position offers a competitive salary range and a comprehensive benefits package, including medical, dental, and retirement options, along with opportunities for professional development.

Work Environment:

This is a full-time position requiring on-campus presence during standard business hours.

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