Clinical Research Coordinator I

Responsibilities

• Lead coordinator on a study
• Execute follow-up visits on ongoing studies
• Query resolution and other study specific tasks
• Perform daily tasks such as document review, data entry, test material preparation and data collection
• Coordinate and execute projects assigned by the Clinic Manager while abiding by Good Clinical Practice (GCP) guidelines
• Set up and conduct study in compliance with protocol, SOPs, applicable regulations and GCPs
• Prepare for and conduct pre-study meetings as well as other meetings and processes as deemed to protocol, SOPs and GCPs
• Monitor Compliance of panelists
• Prepare and be accountable for all Test Material for managed studies
• Adhere to study budget
• Prepare, complete, organize and maintain of all study documentation forms, including drafting protocol amendments, case report forms, Electronic Data Capture (EDC), and other study specific documents
• Assure that staff working on their managed studies understand and are performing duties according to protocol, SOPs and GCPs
• Coordinate scheduling subjects for visits
• Complete other duties or tasks assigned by Clinic Manager and/or Supervisor

Qualifications

• Associate degree or 2 years minimum of relevant work experience with a GED or High School Diploma
• Understands basic concepts in clinical research and capable of learning and performing duties during clinical studies
• Knowledge / Skills / Abilities

Knowledge / Skills / Abilities

• Language Skills
• Mathematical Skills
• Reasoning Skills/Abilities
• Computer Skills
• Ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.

Additional Information

• Salary: $22.00 - $23.00/Hour
• Our Benefits: Health, Wealth, Happiness, Professional Growth, Work-Life Balance
• SGS is an Equal Opportunity Employer