Clinical Research Support Specialist

U.S. Anesthesia Partners; Roanoke (VA); On-site; USD 35,700 - 48,300; Full time

Job summary

Virginia Tech is seeking a Clinical Research Coordinator to support research studies under the supervision of the Principal Investigator. The role involves coordinating with sponsors, IRB submissions, data collection from medical records and questionnaires, and monitoring adherence to study protocols.

The candidate will develop and maintain study logs, assist with informed consent, coordinate site visits, and communicate with participants.

Qualifications

• Previous research experience, preferably with humans.
• Demonstrated organizational skills and acknowledgement of safety protocols.
• Ability to maintain a high level of confidentiality and professionalism.
• Open to working weekends and nights as necessary to meet business needs.
• Demonstrated communication skills.
• Ability to work independently and as part of a team.
• Ability to manage multiple tasks and exceptional time-management skills.

Responsibilities

• Oversee compliance to research protocols; assist with completion and submission of study documents.
• Monitor enrollment goals; coordinate informed consent and screening materials, visits, and liaison with participants.
• Collect data from charts, medical records, interviews, questionnaires, and tests; collect research specimens as directed.
• Track and report adverse events and protocol deviations.
• Coordinate site monitoring or auditing visits by sponsor or federal agencies.
• Prepare, submit, and maintain IRB, OSP, and other regulatory documents.

Skills

Research experience

Human subjects

Organizational skills

Safety protocols

Confidentiality

Communication

Time management

Teamwork

Job description

Virginia Tech is seeking a Clinical Research Coordinator to support research studies under the supervision of the Principal Investigator. The role involves coordinating with sponsors, IRB submissions, data collection from medical records and questionnaires, and monitoring adherence to study protocols.

The candidate will develop and maintain study logs, assist with informed consent, coordinate site visits, and communicate with participants.