Lead Clinical Research Coordinator - Drive Study Execution

SGS; Phoenix (AZ); On-site; USD 50,000 - 65,000; Full time

Job summary

SGS is seeking a Clinical Research Coordinator I to coordinate clinical studies at our Phoenix, AZ facility. You will lead study coordination, perform data entry, document review, and ensure adherence to protocol and GCP guidelines.

The role requires an associate degree or 2 years of relevant experience, with the ability to manage multiple projects in a fast-paced environment and organize CRFs, EDCs, and study materials.

Qualifications

• Associate degree or 2 years of relevant work experience with a GED or high school diploma.
• Basic understanding of clinical research concepts and ability to learn duties during clinical studies.
• Ability to manage and coordinate multiple projects in a fast-paced, professional environment.

Responsibilities

• Lead coordinator on a clinical study and execute follow-up visits for ongoing studies.
• 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 adhering to GCP guidelines and SOPs.
• Perform station and instrumentation duties, collect and record clinical information.
• Respond to queries from Quality Assurance and Statistics; prepare and conduct meetings per protocol and SOPs.
• Prepare test material for studies; maintain study documentation, including CRFs and EDС forms; monitor budgets.
• Ensure staff understand duties per protocol and coordinate scheduling of subject visits.
• Complete additional duties as assigned by Clinic Manager or Supervisor.

Skills

Project coordination

Clinical research knowledge

Multitasking

Education

Associate degree or 2 years relevant experience

Job description

SGS is seeking a Clinical Research Coordinator I to coordinate clinical studies at our Phoenix, AZ facility. You will lead study coordination, perform data entry, document review, and ensure adherence to protocol and GCP guidelines.

The role requires an associate degree or 2 years of relevant experience, with the ability to manage multiple projects in a fast-paced environment and organize CRFs, EDCs, and study materials.