Sr. Clinical Trial Coordinator

MSD (Merck)

Haryana, India
Clinical trial management
Document management
Budgeting and payments
This role is responsible for comprehensive trial and site administration

Job Summary

  • This role is responsible for comprehensive trial and site administration.
  • The CTC supports clinical supply management and ensures timely maintenance of tracking tools.
  • The person acts as process Subject Matter Expert, making recommendations for continuous improvement.

Matching Summary

This role is responsible for comprehensive trial and site administration.

Skills & Requirements

Must-have

  • Clinical trial management
  • Document management
  • Budgeting and payments

Nice-to-have

  • Proactive problem-solving
  • Culturally sensitive relationships
  • Mentoring junior staff

Key Requirements

  • Minimum 3 - 5 years in Clinical Research
  • Bachelor’s Degree or equivalent experience
  • Fluent in local languages and business proficient in English

Work Rights

Not specified

Tailored Resume

Cover Letter