Clinical Research Associate 临床监查员（北京/沈阳/长春/哈尔滨)

RESPONSIBILITIES
• Perform site select******** ******** monitoring an********-out visitsin accordance with contracte******** of work an******** clinicalpractice.
• Provide monitoring visits an******** management for a variety ofprotocols, sites an******** areas.
• Administer protocol an******** study training to assigne********an******** regular lines of communication with sites to
manage ongoing project expectations an********.
• Evaluate the quality an******** of study site practices relate********the proper conduct of the protocol an******** to
applicable regulations. Escalate quality issues to Clinical Team Lead(CTL) and/or line manager.
• Manage the progress of assigne******** by tracking regulatorysubmissions an********, recruitment an********,
case report form (CRF) completion an********, an******** querygeneration an********.
• Create an******** appropriate documentation regarding site management,monitoring visit findings an******** plans by
submitting regular visit reports an******** require********documentation.
• May provide assistance to more less experience******** staff.
All responsibilities are essential job functions unless note********nonessential (N).


REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
• Basic knowledge of, an******** in apply******** applicable clinicalresearch regulatory requirements; i.e., Goo******** Practice
(GCP) an******** Conference on Harmonisation (ICH) guidelines
• In depth therapeutic an******** knowledge as provide******** companytraining
• Computer skills including proficiency in use of Microsoft Word, Excelan******** an******** of a lap top computer
• Strong written an******** communication skills including goo********of English language
• Excellent organizational an********-solving skills
• Effective time management skills
• Ability to manage competing priorities
• Ability to establish an******** effective working relationships withcoworkers, managers an********


MINIMUM REQUIRED EDUCATION AND EXPERIENCE
• Bachelor's degree in a health care or other scientific discipline oreducational equivalent an******** than1 year of on-site
monitoring experience; or equivalent combination of e******** training an********