Clinical Research Coordinator II

Tekton Research

Edmond (OK)

On-site

USD 50,000 - 70,000

Full time

14 days+

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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

The CRC II is responsible for the daily operations and overall management of assigned clinical trials including administrative duties and regulatory functions. Responsible for clear and direct communication with study sponsor, study monitor, CRO, PI and site management. Adherence to Tekton SOPs is required. The CRC II works collaboratively with the CRC I to train and guide them on Tekton SOPs, protocol, and regulatory compliance. It is the responsibility of the CRC II to problem solve issues that may arise and to represent himself/herself and the site in the most professional, ethical and positive manner.

Required Skills/Abilities
  • 2 + years Clinical Research Coordinator experience required
  • Phlebotomy, Vitals, EKG experience required
  • IP management, accountability & administration experience required
  • Ability to work independently and as a member of a team
  • Effective verbal and written communication skills
  • Ability to read, write, and speak English language
  • Knowledge of high-level medical terminology
  • GED or HS Diploma required, advanced training preferred

Mon - Fri / 8am - 5pm

Tekton Research is a growth-oriented research company focused on excellent conduct of clinical trials. We are team-oriented and core value-centric. We value Focus, Discipline, and Accountability. We offer benefits and a competitive salary. At Tekton Research, we do excellent work and are Making Life Better.

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