About the role

  • Clinical Research Associate II performing data abstraction and entry for clinical research. Collaborating with site coordinators and preparing reports while ensuring compliance with protocols.

Responsibilities

  • Act as site study coordinator conducting informed consent process as designated.
  • Assist with protocol submissions for review by federal or institutional committees as applicable.
  • Develop, maintain, monitor, and/or share assigned/relevant documentation.
  • Perform data abstraction, collection, and entry to support clinical research.
  • Prepare submission for all reportable events.
  • Prepare detailed data reports as required.
  • Provide patient care, education, and management as applicable.
  • Perform other duties as assigned to meet the goals and objectives of the department and institution.

Requirements

  • Bachelor's degree in relevant area required.
  • Master's degree preferred.
  • Minimum Requirement: 2+ years of experience in carrying out research preferably in healthcare settings.
  • Experience managing cross-functional communication, including liaison between site and study teams.
  • Some experience with documentation and tracking systems/processes.
  • Proven performance in earlier role.

Benefits

  • Explore our exceptional benefits !

Job title

Clinical Research Associate II – BMT

Job type

Experience level

JuniorMid level

Salary

$70,720 - $126,880 per year

Degree requirement

Bachelor's Degree

Location requirements

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