Clinical Research Coordinator II

Job Description

This position is responsible for the management of subjects on clinical trials and coordinating activities associated with clinical trials.

Essential Functions

• Screens potential subjects for clinical trials through a careful review of the patient’s past medical history and a review of current findings against inclusion and exclusion criteria specific to a trial
• Maintains informed consents records of each patient for the duration of a study
• Captures, processes, and ships biospecimens per sponsor protocol and regulations
• Protects the rights, safety, and welfare of patients
• Strives to maintain harmonious relationships with clinic team members, administrative staff, patients, their caregivers, and the public
• Reviews newly activated protocols, amendments, notices, suspensions, and terminations

Knowledge, Skills & Abilities

• Excellent verbal and written communication skills
• Excellent organization and follow-up skills
• Ability to handle multiple priorities in a fast-paced environment
• Ability to understand complex clinical trials protocols
• Ability to function in multi-functional teams
• Microsoft Office product knowledge (Word, Excel, PowerPoint, etc.)
• Bilingual (English/Spanish) a plus

Education & Experience

• Bachelor’s Degree or equivalent combination of education and experience required
• Two years of relevant experience required