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Transaction coordinator • lafayette la
Clinical Research Coordinator
Southern Urology LafayetteLafayette, LA, USParty Coordinator
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Louisiana State University (LSU)Lafayette, LA, US- software architect (from $ 239,520 to $ 244,260 year)
- intake coordinator (from $ 29,738 to $ 200,000 year)
- machine learning engineer (from $ 142,910 to $ 200,000 year)
- pediatric dentist (from $ 45,760 to $ 200,000 year)
- business development manager (from $ 72,500 to $ 195,000 year)
- engineering director (from $ 39,000 to $ 193,670 year)
- director of engineering (from $ 39,000 to $ 193,250 year)
- telecom engineer (from $ 155,525 to $ 185,150 year)
- telecommunications engineer (from $ 155,525 to $ 185,150 year)
- aerospace engineer (from $ 123,760 to $ 179,000 year)
- Westminster, CO (from $ 37,500 to $ 90,000 year)
- Denver, CO (from $ 45,000 to $ 84,141 year)
- Newark, NJ (from $ 46,219 to $ 76,650 year)
- Los Angeles, CA (from $ 42,000 to $ 75,000 year)
- Santa Rosa, CA (from $ 45,000 to $ 72,500 year)
- Santa Clarita, CA (from $ 45,000 to $ 72,500 year)
- El Monte, CA (from $ 40,000 to $ 69,000 year)
- New York, NY (from $ 37,500 to $ 67,500 year)
- Jersey City, NJ (from $ 36,131 to $ 65,000 year)
- Plano, TX (from $ 37,050 to $ 64,996 year)
The average salary range is between $ 35,895 and $ 55,000 year , with the average salary hovering around $ 42,500 year .
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Clinical Research Coordinator
Southern Urology LafayetteLafayette, LA, US- Full-time
Job Description
Job Description
We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team (RN or LPN) In this role, you will be responsible for overseeing clinical trials and ensuring compliance with regulatory standards. You will work closely with research teams, participants, and sponsors to facilitate the successful execution of clinical studies. The ideal candidate will possess a strong understanding of medical terminology, data management systems, and compliance management.
Responsibilities
- Coordinate and manage all aspects of clinical trials from initiation to completion.
- Conduct blood sampling and ensure adherence to safety standards.
- Oversee data collection processes, ensuring accuracy and integrity of data.
- Review documentation for compliance with regulatory requirements and study protocols.
- Maintain up-to-date knowledge of HIPAA regulations and ensure participant confidentiality.
- Collaborate with investigators to develop study protocols and informed consent documents.
- Monitor trial progress, addressing any issues that arise during the study.
- Prepare reports on study findings and assist in the publication of results.
Requirements
Join us in advancing medical knowledge through rigorous research while ensuring the highest standards of participant care and data integrity.
Benefits :Schedule :
Education :
Experience :
Work Location : In person
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