Radiation Oncology Clinical Research Specialist

University of Maryland Medical System Corporation; Baltimore (MD); On-site; USD 80,000 - 120,000; Full time

Job summary

University of Maryland Medical System Corporation seeks a clinical research professional to coordinate the implementation of approved protocols and support complex trial activities under supervision. This role interfaces with investigators, regulatory bodies and sponsors to ensure compliant study conduct.

The position involves study activation preparation, data collection and analysis, plus training staff. Independent work and strong communication with stakeholders are essential in delivering

Qualifications

• Ability to understand and utilize scientific terminology in communications.
• Lead role in performing various advanced, routine, and maintenance procedures.
• Ability to conduct independent projects and serve as a consultant in technical areas.

Responsibilities

• Submit protocols for review boards and coordinate responses with regulatory bodies.
• Recruit and screen subjects for research studies.
• Prepare studies for activation and develop tools/manuals for departments.
• Perform data collection, entry, verification, analysis and reporting.
• Provide training and guidance to clinical research staff.
• Participate in study design and act as liaison with sponsors and investigators.
• Ensure Good Clinical Practices and CFR compliance.
• Maintain clinical databases and monitor participant safety and continuity of care.

Skills

Clinical Research Coordination

Regulatory Submissions

Independent work

Communication Skills

Data Entry and Verification

Education

Bachelor's degree in epidemiology, sociology, psychology, nursing or related field

Tools

Statistical Software

Spreadsheet Software

Database Software

Job description

University of Maryland Medical System Corporation seeks a clinical research professional to coordinate the implementation of approved protocols and support complex trial activities under supervision. This role interfaces with investigators, regulatory bodies and sponsors to ensure compliant study conduct.

The position involves study activation preparation, data collection and analysis, plus training staff. Independent work and strong communication with stakeholders are essential in delivering