WhatsApp Group
Join Now
WhatsApp Channel
Join Now
Telegram Group
Join Now
Advertisement

Accede Clinicals Hiring For Clinical Research Coordinator

Published on

Accede Clinicals

Bachelor’s or Master’s degree in Pharmacy, Life Sciences

Guwahati, Assam

1–2 Years

Verified Job

Email Application

Why Use Pharmabharat?

Real-Time Job Alerts

Trusted by Top Pharma Employers

Exclusive Pharma Industry Insights

Verified & Trusted Listings

Advertisement

Accede Clinicals, a growing organization in clinical research services, is hiring a Clinical Research Coordinator (CRC) in Guwahati, Assam. This opportunity is ideal for candidates with 1–2 years of hands-on experience in clinical trial coordination, regulatory documentation, and ethics committee (EC) submissions.

If you are looking for a Clinical Research Coordinator job in Guwahati with exposure to end-to-end clinical trial activities, this role offers a strong platform to build your career in clinical research.


🧪 Job Details at a Glance

  • Position: Clinical Research Coordinator (CRC)
  • Company: Accede Clinicals
  • Location: Guwahati, Assam
  • Experience Required: 1–2 Years
  • Industry: Clinical Research / Clinical Trials
  • Job Type: Full-time

🔑 Key Responsibilities – Clinical Research Coordinator

As a Clinical Research Coordinator at Accede Clinicals, your responsibilities will include:

  • Coordinating clinical trial activities as per approved study protocols
  • Thorough understanding and implementation of study protocols
  • Preparation, handling, and maintenance of regulatory and essential documents
  • Managing Ethics Committee (EC) submissions, follow-ups, and approvals
  • Maintaining accurate and complete subject source documents
  • Ensuring compliance with ICH-GCP guidelines and SOPs
  • Supporting investigators during study conduct and audits

🎓 Qualifications & Experience Required

  • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Clinical Research, or related field
  • 1–2 years of experience in clinical trial coordination
  • Practical exposure to EC submissions and regulatory documentation
  • Good understanding of clinical research processes and compliance
  • Strong documentation, communication, and organizational skills

💼 Why Join Accede Clinicals?

  • Hands-on exposure to real-world clinical trial coordination
  • Opportunity to strengthen expertise in regulatory and ethics submissions
  • Work with experienced professionals in clinical research services
  • Career growth in a structured clinical research environment

📩 How to Apply?

Interested and eligible candidates can apply by sending their updated resume to:

📧 Email: hr.ac808@gmail.com

Share This Job

✅ Job Copied Successfully!
Ad Popup