Clinical Research Coordinator - William Cannon

Full Time
Austin, TX
Posted
Job description
Clinical Research Coordinator – Austin, TX – William Cannon Research Site
MediSync Clinical Research is part of our parent company, MediSync, Inc. that is headquartered in Cincinnati, Ohio. We are a strategic and progressive company that values people from all walks of life. MCR provides various clinical research activities in coordination with national pharmaceutical companies. Together with Austin Regional Clinic in Austin, TX we conduct research studies to help make a positive impact in healthcare. We have current opportunities to make a meaningful impact by conducting COVID-19 vaccine studies. The work we do can play a significant role in the quest to combat COVID-19 and emerge from the global pandemic. If you are a talented individual who wants to contribute towards bettering healthcare MCR is the place for you.
We currently have opening for Clinical Research Coordinators at our William Cannon research office in Austin, TX. The Clinical Research Coordinators will be responsible for the overall coordination, organization, and implementation of research studies in compliance with study protocol, SOPs, and state and federal regulations. This role requires the CRC to maintain open, clear, and effective communication with the physicians, patients, study sponsors, Institutional Review Board, and internal management.
Compensation and Benefits:
  • An attractive competitive hourly wage will be offered, which is determined based upon experience. A differential will also be paid for work on COVID-19 studies.
  • Opportunity to earn annual bonus.
  • Company paid Anthem health insurance plan.
  • Dental, vision, life insurance, short and long-term disability, HSA and FSA.
  • 401(k) with immediate eligibility and company provided matching contribution.
  • Paid time off accrued from first day of employment to use for vacations, personal time, and sick time.
  • Wellness program with annual incentives.
Education and Experience:
  • Clinical Research experience as a clinical research coordinator or similar position, 2 years preferred.
  • Bachelor's degree or RN preferred, but will accept some college, highschool/GED, or vocational education in a health care related discipline.
  • Preferred proficiency in clinical procedures such as phlebotomy, vital signs, and ECGs. On-the-job training can be provided.
Knowledge, Skills and Competencies:
  • Knowledge and understanding of general medical terminology; clinical methods, procedures, and applications.
  • Knowledge and understanding of the principles of good clinical practices including ethical issues, patient rights, regulations, and guidelines for clinical research.
  • Excellent written and verbal communication skills.
  • Extensive working knowledge of GCP, ICH, and other research industry norms.
  • Team building.
  • Leadership.
  • Problem solving
  • Customer service.
  • Interpersonal skills.
  • Process improvement.

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