Clinical Research Coordinator II

1 week ago


Norfolk, Virginia, United States Eximia Research Full time

About Eximia Research

Eximia Research is a leading network of research sites dedicated to delivering exceptional clinical research services to the biopharmaceutical, biotechnology, and medical industries.

Job Summary

The Clinical Research Coordinator II is a key member of our team, responsible for managing multiple clinical trials from initiation to completion, ensuring compliance with protocols and industry standards.

Key Responsibilities

  • Conduct and manage clinical trials in accordance with study protocols and guidelines, ensuring timely and accurate data collection.
  • Perform medical procedures within protocol and regulatory requirements, maintaining the highest level of patient care and safety.
  • Coordinate all aspects of assigned clinical trials, from start-up to close-out, including project management, data management, and regulatory compliance.
  • Implement project management concepts to enhance study quality, ensuring seamless execution and timely completion.
  • Communicate effectively with team members, sponsors, and vendors, fostering strong relationships and ensuring seamless collaboration.
  • Ensure data accuracy and resolve queries in a timely manner, maintaining the highest level of data integrity.
  • Maintain confidentiality of sensitive information, adhering to strict confidentiality agreements and protocols.
  • Evaluate and recruit potential study subjects, ensuring compliance with regulatory requirements and study protocols.
  • Adhere to regulatory requirements and submit necessary documents, ensuring compliance with industry standards.
  • Collaborate with the team to ensure quality control and prepare for monitoring visits, ensuring a seamless and efficient process.
  • Perform clinical duties as required, maintaining a high level of professionalism and expertise.

Qualifications

To be successful in this role, you will require:

  • A Bachelor's degree with 2 years of relevant experience, or an Associate's degree with 4 years of relevant experience, or a High School Graduate with 6 years of relevant experience and 1 year as a Clinical Research Coordinator.
  • Phlebotomy certification if applicable, Intramuscular dose administration certification if applicable, and Certified Clinical Research Coordinator through ACRP or SOCRA within six months.
  • Strong knowledge of medical terminology, proficiency in technology use, and ability to work in a fast-paced environment.
  • Strong communication and organizational skills, with the ability to work effectively in a team environment.
  • Detail-oriented with leadership skills, with the ability to problem-solve and make sound decisions.


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