From Top Pharmaceutical Company with Amazing Managing Team

Your new company
Top pharmaceutical company in cardiology and ophthalmology areas with great managing group from top MNC

Your new role
Conducts monitoring (pre-study, initiation, routine monitoring and closeout visit), if require

Conducts co-monitoring visits, if required

Conducts Quality Oversight Visits (QOV), as requested

Completes monitoring visit/ QOV reports timely

Assists with investigator/site identification

Assists site to prepare Ethics Committee submissions

Facilitates clinical trial site contract and budget negotiation

Manages site queries and communications

Assists in managing clinical trials, if required

Establishes regular lines of communication with sites and PMs

Provides protocol and related study training to assigned sites

Evaluates the quality and integrity of site practices – escalating quality issues as appropriate

Manages site performance by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

What you'll need to succeed
Bachelor’s level degree or above in life sciences, pharmacy, nursing or medical

Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines

2 years or more monitoring experience in the Pharmaceutical or CRO industry

Excellent communication and interpersonal skills

Excellent organizational skills and ability to prioritise and multi-task

Fluent in English (writing and speaking)

What you'll get in return
Excellent working experience in top pharmaceutical company with amazing team

Great exposure to the frontier of clinical areas

Exciting growth opportunities

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. #1216697


Job Type
Life Sciences

Talk to a consultant

Talk to Olivia Huo, the specialist consultant managing this position, located in Beijing
501, Tower 1, China Central Plaza, 81 Jianguo Road, Chaoyang District

Telephone: 01086487955

Similar jobs to CRA II,SCRA

  • Associate Clinical Project Manager

    From Top Pharmaceutical Company with Amazing Managing Team Focusing on Hot TA
  • Research Scientist

    Leading pharmaceutical company