Clinical Research Coordinator II — Lead, Compliance & Operations

Tekton Research; Edmond (OK); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

Competitive salary

Comprehensive benefits

Job summary

Tekton Research in Edmond, Oklahoma is looking for a Clinical Research Coordinator II to oversee daily operations of clinical trials. Responsibilities include managing communications with sponsors, monitors, and site management, while ensuring adherence to SOPs and training CRC I personnel.

The ideal candidate has a minimum of two years of experience in clinical research and must possess skills in phlebotomy and effective communication. We offer competitive salaries and comprehensive benefits in a collaborative work environment.

Qualifications

• 2+ years of experience as a Clinical Research Coordinator is needed.
• Experience in phlebotomy, vitals, and EKG is required.
• Ability to work both independently and as part of a team.

Responsibilities

• Manage daily operations and overall management of clinical trials.
• Communicate clearly with study sponsors and site management.
• Train and guide CRC I on protocols and regulatory compliance.

Skills

Clinical Research Coordinator experience

Phlebotomy

Effective communication skills

Knowledge of medical terminology

Education

GED or HS Diploma

Advanced training

Job description

Tekton Research in Edmond, Oklahoma is looking for a Clinical Research Coordinator II to oversee daily operations of clinical trials. Responsibilities include managing communications with sponsors, monitors, and site management, while ensuring adherence to SOPs and training CRC I personnel.

The ideal candidate has a minimum of two years of experience in clinical research and must possess skills in phlebotomy and effective communication. We offer competitive salaries and comprehensive benefits in a collaborative work environment.