Clinical Research Assistant - Oncology - Per Diem

Essential Duties & Responsibilities

• Prepare, organize, and maintain ISF, Pharmacy, and Lab Binders from study start up through trial closeout.
• Print clinical trial related documents and correspondence and file in the appropriate clinical trial regulatory, lab, and pharmacy binders, as applicable.
• Unpack and organize clinical trial lab kits.
• Obtain physician and research team member signatures on trial related documents.

Required Knowledge, Skills & Abilities

• Consistently arrives at work in appropriate/professional attire.
• 1-2 years administrative experience in supporting daily operations, communication, scheduling, and record-keeping in an organization.
• Must have well developed verbal and non-verbal communication skills.
• Must have excellent organization and problem-solving abilities.
• Strong customer service and team orientation essential.
• Must be a team player, flexible and able to handle multiple tasks.
• Must have appropriate computer skills, which include Microsoft Office, Word, and Internet Skills.
• Demonstrate required work ethics and integrity of research data, and appropriate patient confidentiality.
• Completes all tasks within established time frame.
• Adheres to all clinic policies and procedure.
• Able to adapt to different working environments.
• Sets appropriate tasks when primary tasks are completed and assists co-workers as needed.
• Demonstrates adaptability to expanded roles.

Education

• High school diploma preferred.
• Knowledge of oncology related medical terminology.