Advity Research Hiring Clinical Trial CRA in Hyderabad

Advity Research, a reputed name in clinical research and pharmaceutical development, is inviting talented professionals to join its growing team. The company has announced openings for the position of Clinical Trial CRA (Clinical Research Associate) at its Hyderabad location.

About the Company
Advity Research is known for its commitment to scientific excellence, ethical research practices, and innovation in clinical development. With a vision to “Add Value with Integrity,” Advity continues to contribute to global healthcare advancements through high-quality research and reliable clinical trial management.

Position: Clinical Trial CRA

Location: Hyderabad
Job Type: Full-Time
Mode of Work: On-Premise

Experience Required
2 to 4 years of experience in clinical research or related roles.

Candidates with hands-on exposure to clinical trial monitoring, site coordination, and GCP (Good Clinical Practice) guidelines will be preferred.


Educational Qualification
B.Pharmacy / M.Sc / Pharm.D / M.Pharmacy
Applicants should have a strong understanding of clinical trial processes, documentation, and regulatory compliance.


Required Skills
•Excellent communication and organizational abilities.
•Strong fluency in English (spoken and written).
•Attention to detail and a proactive approach to managing trial activities.

Key Responsibilities
•Monitoring clinical trials and ensuring protocol adherence.
•Coordinating with investigators, clinical sites, and project teams.
•Reviewing and verifying case report forms (CRFs) and essential documents.
•Maintaining compliance with GCP and ethical standards.

How to Apply
Interested candidates can send their updated resumes to:
📧 hr@advityresearch.com
Please mention “Application for Clinical Trial CRA” in the subject line.

Why Join Advity Research?
At Advity, employees are part of a purpose-driven organization where innovation meets integrity. The company offers professional growth opportunities, collaborative work culture, and exposure to international clinical research standards.