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CRA, Medical Writer & QA Openings at Ardent CRO

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Ardent CRO

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Medicine

Pune/ Hyderabad

2 - 6 Years

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Ardent CRO is a leading clinical research organization (CRO) dedicated to advancing healthcare through high-quality clinical trials and regulatory compliance. With a strong presence in Pune and Hyderabad, we offer a dynamic work environment, career growth, and opportunities to work on global clinical research projects.

Current Job Openings

We are looking for talented professionals to join our team in the following roles:

1. Clinical Research Associate (CRA)

๐Ÿ“ Location: Pune / Hyderabad
๐Ÿงช Experience: 2โ€“3 years

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Key Responsibilities:

  • Conductย site monitoringย (initiation, routine, and close-out visits).
  • Ensure compliance withย ICH-GCP and CDSCO regulations.
  • Manage multiple trial sites and ensure timely documentation.
  • Willingness toย travel frequentlyย for site visits.

Eligibility:

  • Degree inย Life Sciences/Pharmacy/Medicine.
  • Hands-on experience inย clinical trial monitoring.
  • Strong understanding ofย regulatory guidelines.

2. Medical Writer โ€“ Clinical Research

๐Ÿ“ Location: Pune / Hyderabad
๐Ÿงช Experience: 3โ€“5 years

Key Responsibilities:

  • Draftย clinical study reports (CSRs), protocols, IBs, ICFs, and regulatory documents.
  • Ensure compliance withย ICH-GCP and global regulatory standards.
  • Collaborate with cross-functional teams for accurate documentation.

Eligibility:

  • Advanced degree inย Life Sciences/Pharmacy/Medicine.
  • Excellentย scientific writing & communication skills.
  • Prior experience inย regulatory medical writing.

3. Manager โ€“ Quality Assurance (QA)

๐Ÿ“ Location: Pune / Hyderabad
๐Ÿงช Experience: 5โ€“6 years

Key Responsibilities:

  • Conductย GCP audits, SOP reviews, and CAPA management.
  • Performย site/vendor auditsย to ensure compliance.
  • Maintainย regulatory documentationย and quality standards.

Eligibility:

  • Strong background inย GCP/GXP compliance.
  • Experience inย clinical trial audits & quality systems.
  • Detail-oriented with strongย documentation skills.

Why Join Ardent CRO?

โœ… Competitive salary (No bar for eligible candidates)
โœ… Career growth & learning opportunities
โœ… Work on global clinical research projects
โœ… Flexible & supportive work culture

How to Apply?

Interested candidates can send their resumes to hr@ardent-cro.com with the job title in the subject line.

๐Ÿ“Œ Donโ€™t miss this opportunity to advance your career in clinical research!

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