Senior Clinical Research Coordinator

Responsibilities

• Manage all aspects of a study from planning through closeout
• Conduct research protocols in accordance with Good Clinical Practice Guidelines
• Participate in the informed consent process
• Coordinate and perform all study visit procedures per protocol
• Manage data entry, query resolution, and Investigational Product management
• Manage study-related supplies and equipment
• Host monitoring visits and attend investigator meetings
• Provide high-level care for study patients and customer service to pharmaceutical clients

Requirements

• Minimum of two years of experience as a Clinical Research Coordinator on clinical trials
• Experience in hands-on patient-facing clinical roles
• Strong organizational and communication skills
• Ability to manage multiple studies as a primary coordinator

Preferred Qualifications

• Nursing license
• Medical assistant certificate or registration
• Experience with sponsor-initiated and pharma clinical trials

Benefits

• PPO and HMO medical plans
• PPO and HMO dental plans
• Vision coverage
• Long term disability plan
• Life/AD&D coverage
• 401k plan
• Paid holidays and paid time off

About the Company

Artemis Institute for Clinical Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments, specializing in Psychiatry/Neurology, Internal Medicine, and Women’s Health studies.