JOB SUMMARY

The Clinical Research Coordinator plays a pivotal role in the management and execution of clinical trials. This position involves overseeing the daily operations of research studies, ensuring compliance with regulatory standards, and maintaining the integrity of data collected. The ideal candidate will possess a strong understanding of medical terminology and research methodologies, along with excellent organizational and communication skills.

SKILLS

• Strong knowledge of medical terminology and clinical research standards.
• Proficiency in patient monitoring techniques and vital signs assessment.
• Experience with documentation review processes to ensure adherence to protocols.
• Familiarity with statistical software for data analysis is preferred.
• Ability to supervise team members effectively while fostering a collaborative environment.
• Understanding of HIPAA regulations to protect patient confidentiality.
• Experience in blood sampling techniques is a plus.
• Excellent organizational skills with attention to detail in managing multiple tasks.
  This role is essential for advancing clinical research initiatives while ensuring high-quality patient care. If you are passionate about contributing to medical advancements through research, we encourage you to apply.
  Job Type: Contract
  Pay: $33.84 - $36.10 per hour
  Expected hours: 40 per week

Benefits:

• Referral program

Medical Specialty:

• Oncology

Schedule:

• Day shift
• Monday to Friday

Experience:

• Clinical research: 4 years (Required)

License/Certification:

• BLS Certification (Required)

Work Location: On the roa

• Coordinate and manage clinical trials from initiation through completion.
• Ensure compliance with regulatory standards, including HIPAA regulations.
• Monitor patient safety and well-being throughout the study, including vital signs and blood sampling as necessary.
• Conduct documentation review to ensure accuracy and completeness of study records.
• Supervise research staff and provide training on study protocols.
• Maintain accurate records of patient interactions and data collection.
• Utilize statistical software for data analysis and reporting findings.
• Collaborate with investigators, sponsors, and other stakeholders to facilitate smooth study operations.