Clinical Research Associate Jobs in Advity Research Pvt. Limited - Hyderabad, Telangana

Clinical Research Associate Jobs in Advity Research Pvt. Limited - Hyderabad, Telangana

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Advity Research Pvt. Limited

time outline iconHyderabad, Telangana, India

Posted on 28-01-2026

1 Vacancy

Description

  1. Job Title: Clinical Research Associate
  2. Qualification: BPharm/MPharm
  3. Location: Advity Research Pvt. Limited - Hyderabad, Telangana
  4. Work Experience: 0 to 5 Years

Job Description

  1. Monitor clinical trial sites as per protocol and SOPs.
  2. Ensure patient safety and data integrity.
  3. Verify source documents and CRFs.
  4. Ensure informed consent is properly obtained.
  5. Track and report adverse events and protocol deviations.
  6. Maintain Trial Master File (TMF) and site files.
  7. Coordinate with investigators and site staff.
  8. Prepare monitoring visit reports (pre & post visit).
  9. Ensure regulatory and ethical compliance.
  10. Support audits and inspections.

Take this opportunity to join Advity Research Pvt. Limited - Hyderabad, Telangana as a Clinical Research Associate in Hyderabad, Telangana and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Clinical Research/ Data Science

Preferred Education

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

Good Communication SkillsTime Management SkillsInterpersonal skillsTeamwork

About Organization

Advity Research Pvt. Limited, Hyderabad, Telangana, is a reputed pharmaceutical and clinical research organization committed to ethical research practices, quality standards, and regulatory compliance. The company is inviting applications for Clinical Research Associate Jobs as part of its expanding clinical research team. The role involves monitoring clinical trials, ensuring protocol adherence, managing trial documentation, coordinating with investigators and study sites, and ensuring compliance with GCP and regulatory guidelines. This opportunity offers strong clinical research exposure, professional development, and long-term career growth in a structured and supportive research environment.

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