Opportunity Alert: Join Ethyra Global Research Solutions as a Clinical Research Coordinator (CRC) πŸ₯

Are you a Life Sciences or Pharmacy graduate looking to kickstart or elevate your career in the clinical research industry? Ethyra Global Research Solutions is currently expanding its team and hiring passionate individuals for the role of Clinical Research Coordinator (CRC).

This is a fantastic opportunity to work at the heart of clinical trials, helping ensure life-saving medical advancements are developed with the highest standards of safety and ethics.

Understanding the Role: What Does a Clinical Research Coordinator Do? πŸ€”

A Clinical Research Coordinator (CRC) is the backbone of any clinical trial site. They bridge the gap between the study sponsor, the hospital or clinic (the site), and the patients (the participants).

If you enjoy a mix of administrative precision and direct human interaction, this role could be the perfect fit.

At Ethyra Global Research Solutions, a CRC is expected to handle a diverse range of responsibilities that keep a trial running smoothly and ethically.

Key Responsibilities Include:

πŸ“‹ Trial Coordination & Site Management

You will manage day-to-day clinical site operations, including scheduling patient visits, maintaining trial supplies, and ensuring the facility meets all study requirements.

🀝 Patient Recruitment & Informed Consent (ICF)

You will help identify eligible participants and conduct the Informed Consent Form (ICF) process so every patient fully understands the study before joining.

✍️ Documentation Excellence

Maintain accurate and compliant study records including:

  • Source Documents
  • Case Report Forms (CRFs)
  • Site Master File (SMF)

βš–οΈ Compliance & Ethics

Ensure all trial activities follow ICH-GCP (Good Clinical Practice) guidelines, protocol requirements, and regulatory standards.

πŸ”Ž Monitoring & Audits

Support monitoring visits by Clinical Research Associates (CRAs) and assist during audits/inspections.


Are You Eligible? πŸŽ“

Educational Requirements:

  • B.Sc / M.Sc in Life Sciences (Biotechnology, Microbiology, Zoology, etc.)
  • B.Pharm / M.Pharm / Pharm D

Skills & Knowledge:

  • Freshers are welcome!
  • Candidates with prior clinical trial experience are encouraged to apply.
  • Basic understanding of GCP and clinical trial processes preferred.

Hiring Locations πŸ“

Openings are available across multiple cities in India:

  • Amravati
  • Indore
  • Jabalpur
  • Bhopal

This creates excellent opportunities for local candidates and those willing to relocate.


Why Choose a Career in Clinical Research? 🌟

India’s clinical research industry is growing rapidly. Starting as a CRC can lead to future opportunities such as:

  • Clinical Research Associate (CRA)
  • Trial Start-up Specialist
  • Project Coordinator
  • Clinical Operations Manager
  • Project Manager

It offers both career stability and the satisfaction of helping bring new treatments to patients.


How to Apply πŸ“©

Send your updated CV/Resume to:

πŸ“§ Email: ethyraglobal.research@gmail.com

Tip: Mention your preferred location in the subject line.


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