Senior Clinical Research Associate

Syngene International Ltd

Bangalore, India
On-site
Gcp guidelines and regulations adherence
Site selection and monitoring
Protocol and study training administration
Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work, Standard Operating Procedures and all the applicable Good Clinical Practice (GCP) Guidelines and Regulations

Job Summary

  • Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work, Standard Operating Procedures and all the applicable Good Clinical Practice (GCP) Guidelines and Regulations.
  • Manage the progress and performance of the assigned study sites by following activities but not limited to: tracking regulatory and Ethics Committee submissions and approvals, subject recruitment, case report form (CRF) completion and submission, and data query generation and resolution.
  • All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism.

Matching Summary

Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work, Standard Operating Procedures and all the applicable Good Clinical Practice (GCP) Guidelines and Regulations.

Skills & Requirements

Must-have

  • GCP Guidelines and Regulations adherence
  • site selection and monitoring
  • protocol and study training administration
  • quality and integrity assurance
  • manage study site progress

Nice-to-have

  • good communication skill
  • good team player
  • dynamic, ambiguous environment
  • develop new ideas and creative solutions
  • focused employee

Key Requirements

  • Experience as a Senior Clinical Research Associate
  • M. Sc/M. Pharm/Pharm D, BAMS, BDS, MDS & BHMS/Any life science

Work Rights

Not specified

Tailored Resume

Cover Letter