Clinical Research Assistant - 251480

Clinical Research Assistant

Must Haves: Must have experience as a Clinical Research Assistant, and experience with Oncology

Hours: 40 hours per week, Monday-Friday, onsite, normal business hours. Need someone flexible to come in earlier or stay later for patient needs.

Contract Duration: Permanent position

Benefits: Medical, Dental, Vision, time off, paid holidays off, bonus, 401k, growth opportunities, etc.

Responsibilities

The Research Assistant I is an essential team member in the conduct and execution of clinical research studies. The Research Assistant is to assist under direct supervision of the Site Director or Clinical Research Coordinator (CRC) in clinic supporting activities and perform duties and procedures related to the start-up, conduct and close-out phases of clinical research protocols. Under direct supervision and direction, to help obtain clean, objective, and accurate data within provided timelines while following applicable federal regulations, medical ethics, Good Clinical Practices (GCPs), Institutional Review Board (IRB) requirements, and in compliance with specific sponsor protocol requirements. All responsibilities should be completed in accordance with the companies Mission Statement and Employee Manual.

Required Skills

• Education: Associate in Science degree or adequate experience within the field of clinical research to compensate. Bachelor's degree preferred.
• Experience: Preferably a minimum of 1-3+ years’ experience within the field of clinical research or biological research. Must have experience with Oncology.

Preferred Skills

• Exceptional knowledge of clinical research methods.
• Demonstrates core values & all skills set required.
• Demonstrated ability to collaborate and align with all research department teams.
• Excellent oral and written communication skills.
• Excellent computer skills to include Office365 products.
• Is moral and ethical in decision-making and during interaction with patients, sponsor and IRB representatives, physicians and staff at satellite clinics, and other employees.
• Must be professional, have a strong work ethic, be motivated to identify tasks that need to be completed and to strive for accuracy and quality when completing assignments.
• ECG, phlebotomy skills, and any other technical skills related to the completion of a study visit as required by the protocol.
• Must be able to adapt and take on additional tasks as requested.
• Assists with key initiatives/process improvements in the department.
• Assists with training company new hires.
• Completes at least 80% of goals annually.

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