Clinical Research Coordinator, On-Site, Elkhorn, Nebraska

IQVIA • Omaha, NE

418d • $43,500 - $72,500

About The Position

The Clinical Research Coordinator (CRC) will play a vital role in assisting with the conduct of clinical trial activities at IQVIA's Elkhorn, Nebraska site. This position involves coordinating studies, developing patient recruitment strategies, and ensuring compliance with regulatory guidelines. The CRC will work closely with study team members to achieve study objectives and corporate goals, while maintaining effective communication and strong interpersonal relationships.

Requirements

• Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
• Clinical Research Coordinator experience within a similar setting.
• Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc.
• Knowledge and experience of site operations and the drug development process.
• Effective communication skills.
• Computer proficiency in Microsoft Word and Excel.

Responsibilities

• Coordinate as primary CRC on 1-3 studies of low to medium complexity with oversight by a manager or higher-level CRC.
• Assist as back-up CRC on other studies.
• Develop and implement patient recruitment strategies to achieve enrollment targets.
• Obtain informed consent from research subjects.
• Develop strong working relationships and maintain effective communication with study team members.
• Complete all protocol-related training.
• Perform patient/research participant scheduling.
• Collect patient/research participant history and maintain source documentation.
• Manage inventory and administer test articles/investigational product to participants.
• Perform data entry and query resolution.
• Support the collection and review of required essential study documents and reports.
• Order supportive study supplies such as contracts, lab kits, and handling manuals.
• Adhere to an IRB approved protocol and support the safety of research subjects by reporting adverse events.
• Coordinate protocol-related research procedures, study visits, and follow-up activities.
• Facilitate pre-study, site qualification, study initiation, monitoring visits, and study close-out activities.
• Collect, process, and ship laboratory specimens.
• Perform special project responsibilities and travel to other clinic locations as needed.
• Comply with Avacare and Sponsor policies, standard operating procedures (SOPs), and guidelines.

Benefits

• Health insurance
• 401k plan
• Paid time off
• Professional development opportunities
• Flexible scheduling options

What This Job Offers

• Job Type: Part-time
• Career Level: Entry Level
• Industry: Professional, Scientific, and Technical Services
• Education Level: No Education Listed
• Number of Employees: 5,001-10,000 employees