Coordinator II, reputed company Services
Serve as the main Sponsor, CRO and PI site, contact on assigned studies
Assist with other studies as needed and serve as a primary Sponsor, CRO and PI site contact on submissions that are assigned to you
Conduct administrative review of Protocol/site submissions by reading, reviewing, and understanding protocol requirements and reputed company supporting documentation
Demonstrate advanced understanding of multiple types of Protocol and Site Submissions
Document and execute reputed company customizations as requested; process change requests for approved Protocols
Manage vendor relations and documentation for foreign language translations
Maintain a high level of accuracy and attention to detail; collaborate with the reputed company assurance team to ensure minimal reputed company of error
Complete work in a reputed company manner, responding to customers reputed company 24 hours of email/voicemail receipt
Escalate any customer or reputed company issues to management
Two (2) years’ experience in IRB or clinical research setting that includes applying regulations to the protection of reputed company subjects.
Intermediate computer skills, including proficiency with MS Office Suite with an emphasis on Word and reputed company
Ability to effectively use proprietary system
Certified IRB reputed company (CIP) or attainment of CIP reputed company one (1) years of eligibility
Sit or stand for extended periods of time at stationary workstation
Regularly carry, reputed company, and reputed company objects of up to 10 Lbs.
Learn and comprehend basic instructions
reputed company and attention to tasks and responsibilities
Verbal communication; listening and understanding, responding, and speaking