Clinical Research Coordinator 1 - Hematology/Oncology

Responsibilities

• Covers all aspects of conducting clinical trials including screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports.
• Maintains accurate and complete documentation of signed informed consent, relevant IRB approvals, source documentation, case report forms (CRF's), drug dispensing logs, and study related communication.
• Plans and coordinates patient schedule for study procedures, return visits, and study treatment schedules.
• Ensures standard operating procedures (SOP) are implemented and documented in accordance to study sponsor, primary investigator, and regulatory agency specifications.
• Prepares and maintains protocol submissions and revisions.
• Edits and educates patients about study procedures to be performed, visit schedule, what to report between and during visits, and potential side effects.
• Performs assessments at visits and monitors for adverse events.
• Organizes and attends site visits from sponsors and other relevant study meetings.
• May recruit and interview potential study patients.
• May obtain, possess, and transport specimens to appropriate laboratory according to established aseptic techniques.
• Collaborates in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
• Analyzes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
• Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.

Requirements

• Minimum requirements include a college or university degree in related field.
• Knowledge and skills developed through < 2 years of work experience in a related job discipline.

Qualifications

• Education: Bachelor's degree.
• Technical Skills Or Knowledge: Knowledge of medical terminology/environment, knowledge of Microsoft Word, Excel and Adobe Acrobat, understand complex documents, such as clinical trials.

Skills

• Interacts and communicates with clarity, tact, and courtesy with patrons, patients, staff, faculty, students, and others.
• Communicates with tact and diplomacy.
• Strong organizational skills.
• Strong communication skills, verbal and written.
• Excellent interpersonal skills.
• Strong data management skills and attention to detail.
• Handles competing demands with diplomacy and enthusiasm.
• Absorbs large amounts of information quickly.
• Adapts to changing working situations and work assignments.

Benefits

• Benefits Eligible Yes

Pay

$50,000.00 - $65,000.00