Clinical Research Coordinator

at  The IMA Group

COMPANY OVERVIEW:

The Clinical Research Division at The IMA Group is a dynamic hub of expertise and innovation, dedicated to advancing healthcare through clinical trials and studies. Our team of seasoned professionals collaborates with industry leaders, conducting patient-centric research across diverse therapeutic areas. Committed to ethical practices and regulatory compliance, we aim to pioneer groundbreaking medical solutions that shape the future of healthcare.

JOB SUMMARY:

IMA Clinical Research is seeking an experienced Clinical Research Coordinator with proficiency in managing clinical trials and a background in phlebotomy. They are eagerly seeking individuals like you to become an integral part of our team in NYC!

EDUCATION AND EXPERIENCE:

• Preferably clinical experience in healthcare settings.
• Proficient in conducting and interpreting clinical and diagnostic tests (such as vital signs, height, weight, temperature, etc.) preferred.
• Capable of independent work, leading studies, and making informed decisions.
• Strong team player with proactive problem-solving skills.
• Exceptional communication, professional demeanor, and high motivation.

QUALIFICATIONS:

• At least two years of clinical research and phlebotomy experience.
• Preferred Clinical Research Coordinator certification (CCRC).
• Proficient in leading multiple concurrent projects.
• Bachelor’s degree required; significant demonstrated experience or a master’s degree is preferred.

RESPONSIBILITIES:

• Coordinating clinical trials according to sponsor protocols and ensuring adherence to SOPs.
• Acquiring and maintaining comprehensive knowledge of study protocols and associated procedures.
• Effectively communicating with various stakeholders within the research industry, including sponsors, CROs, monitors CRAs, IRBs, laboratories, and clinical personnel.
• Advising Investigator and staff on protocols and procedures essential for successful study implementation and completion.
• Timely notification of adverse events or serious adverse events as per the protocol.
• Upholding ALCOA principles for accurate and timely documentation, including meticulous data entry.