Search by job, company or skills

Clinical Research Associate

Clinical Research Associate

Flexiple
2-6 Years
Not Disclosed
  • Posted 12 hours ago
  • Be among the first 10 applicants

Job Description

Clinical Research Associate

A hospital group's shared back-office team, covering four of its units, hiring for its clinical operations team

Location: Remote (India)

Who is hiring

A hospital group's shared back-office team, covering four of its units, hiring for its clinical operations team. The team supports four hospitals, so requests arrive from many directions at once. It has partnered with Flexiple to hire a clinical research associate. Flexiple is a managed talent marketplace that places vetted professionals with companies in India and abroad.

The job in short

The associate monitors trial sites, checks that studies follow the protocol and good clinical practice, and keeps data and records reliable. The hospitals host investigator-led and sponsored studies, and the associate supports their site teams.

What the associate handles

  • Carry out site initiation, monitoring and close-out activities as assigned
  • Verify data against source documents and resolve queries
  • Check compliance with the protocol, ICH-GCP and local regulations
  • Review informed-consent and safety-reporting processes
  • Maintain trial master file documents and site files
  • Write monitoring visit reports and follow up on actions
  • Support investigators and site staff with training and questions

Background we need

  • 2 to 6 years in clinical trial monitoring or clinical operations
  • Bachelor's or master's degree in life sciences, pharmacy or medicine
  • Experience in clinical monitoring or clinical operations
  • Working knowledge of ICH-GCP and Indian clinical-trial regulations
  • Careful documentation and good attention to detail
  • Willingness to travel to sites

Additional strengths

  • Experience with an eTMF or EDC system
  • Therapeutic experience in oncology, cardiology or diabetes
  • Formal GCP certification

What the seat gives

  • A Clinical Research Associate seat at a hospital group, reporting to the clinical project manager
  • On-site in Delhi or Hyderabad, with a placement intended to be long term
  • Varied trial exposure across sites and therapy areas

Steps to hire

Screening call, assignment, team panel, final fit conversation.

There is no need to apply twice; a single application is checked against our other openings as well.

More Info

Job Type:
Industry:
Employment Type:

Key Skills

ICH-GCP

eTMF

EDC system

Indian clinical-trial regulations

About Company

Similar Jobs

0-2 yrs
India
Skills:
case report forms , ICH-GCP, site files, protocol compliance
5-7 yrs
Bengaluru, India
Skills:
Site management, Safety reporting, Data quality management, Regulatory Submissions, Source data verification, Ethics committee communications, Clinical Trial Monitoring, Regulatory Compliance, Risk-based monitoring
3-6 yrs
Bengaluru, Mumbai
Skills:
Regulatory & GCP Compliance, Project & Site Management, source data verification (SDV), Clinical Trial Monitoring, Good Clinical Practice, Administer protocol