Senior Clinical Trials Coordinator — Multi-Trial Oversight

Socket.dev; Lenexa (KS); On-site; USD 65,000 - 85,000; Full time

Job summary

JCCT seeks a Clinical Research Coordinator II to manage multiple concurrent clinical trials, ensuring protocol compliance and accurate documentation. You will serve as the main contact for sponsors and investigators, coordinate study activities, and train team members to uphold study standards.

Responsibilities include patient screening, data entry into Medidata Rave, reporting adverse events, and audits support, with a strong emphasis on ethics, ALCOA+ principles, and cross-functional

Qualifications

• BS/BA in Life Science or related discipline or equivalent work experience.
• Basic understanding of CFR, GCP, HIPAA regulations.

Responsibilities

• Develop strong relationships with clinic and sponsor for activities.
• Manage multiple concurrent trials
• Mentor and train study team members
• Maintain study records and regulatory forms
• Screen volunteers for eligibility
• Coordinate Lab procedures and findings with Investigators
• Educate volunteers on study procedures and diary completion
• Ensure training and documentation for protocol amendments and ICFs
• Communicate with Nursing staff and Investigators on study progress
• Track enrollment status in Clinical Conductor or similar systems
• Prepare for QA audits conducted by sponsors or regulators
• Collect, process and ship laboratory specimens
• Adhere to safety and privacy regulations

Skills

Bilingual (Spanish & English)

Excellent communication

Interpersonal skills

Analytical thinking

Problem solving

MS Office proficiency

Education

BS/BA in Life Science or related field

Tools

Medidata Rave

Inform

TrialKit

Job description

JCCT seeks a Clinical Research Coordinator II to manage multiple concurrent clinical trials, ensuring protocol compliance and accurate documentation. You will serve as the main contact for sponsors and investigators, coordinate study activities, and train team members to uphold study standards.

Responsibilities include patient screening, data entry into Medidata Rave, reporting adverse events, and audits support, with a strong emphasis on ethics, ALCOA+ principles, and cross-functional