Clinical Research Coordinator

About the Role

Following established policies, procedures, and study protocols, provides assistance on clinical research studies. Candidates who are in the process of completing their bachelor's degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification. This position does not require patient care.

Responsibilities

• Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
• Recruits patients for clinical trials and conducts phone interviews.
• Verifies the accuracy of study forms and updates them per protocol.
• Prepares data for analysis and data entry.
• Documents patient visits and procedures.
• Assists with regulatory binders and QA/QC procedures.
• Assists with interviewing study subjects.
• Assists with study regulatory submissions.

Requirements

• Bachelor's degree in a related field of study (or equivalent experience).
• 0-1 year of relevant research project work preferred.
• Careful attention to detail and good organizational skills.
• Ability to follow directions and work with clinical research protocols.
• Good interpersonal and communication skills.
• Computer literacy.
• Ability to demonstrate respect and professionalism for subjects' rights and individual needs.

Benefits

In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable, and recognition programs designed to celebrate your contributions and support your professional growth.

Pay

$21.00 - $29.01/hour (Grade 5). Base pay is determined by skills, relevant experience, education, certifications, and other essential factors.

Schedule

• Onsite at 1575 Cambridge Street.
• Scheduled weekly hours: 40.
• Employee type: Regular.
• Work shift: Day (United States of America).