Ardent CRO Hiring Clinical Research Associate, Medical Writer, QA Manager

Ardent CRO Hiring Clinical Research Associate, Medical Writer, QA Manager
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Explore exciting job opportunities at Ardent CRO for Clinical Research Associate, Medical Writer, and QA Manager roles in Pune and Hyderabad. Candidates with qualifications in life sciences, pharmacy, or clinical research and relevant experience are encouraged to apply.

Ardent CRO Hiring CRA, Medical Writer, QA Manager | Pune & Hyderabad


Exciting Job Vacancies at Ardent CRO – Clinical Research Careers in Pune & Hyderabad

Ardent CRO, a reputed name in the field of Contract Research, is inviting skilled professionals for multiple full-time positions in its Pune and Hyderabad offices. If you have an educational background in Life Sciences, Pharmacy, Biotechnology, or Clinical Research, and a passion for advancing healthcare through clinical trials and research, this is your opportunity to grow with a fast-paced, globally aligned organization.

Clinical Research Associate (CRA)

Location: Pune / Hyderabad
Experience Required: 2–3 years

Key Responsibilities:

  • Conduct end-to-end site monitoring from initiation through close-out
  • Ensure compliance with ICH-GCP and CDSCO regulations
  • Coordinate with investigators and site staff for smooth trial operations
  • Prepare visit reports, follow-ups, and maintain essential documents

Preferred Qualifications:

  • Bachelor’s or Master’s in Life Sciences, Pharmacy, or Clinical Research
  • Proficient in regulatory guidelines and site management
  • Strong interpersonal and communication skills

Medical Writer – Clinical Research

Location: Pune / Hyderabad
Experience Required: 3–5 years

Key Responsibilities:

  • Develop and edit clinical documents such as Protocols, CSRs, Investigator Brochures (IBs), Informed Consent Forms (ICFs), and Regulatory Submission Documents
  • Ensure adherence to ICH-GCP and international regulatory standards
  • Collaborate with clinical teams and sponsors

Preferred Qualifications:

  • M.Sc., M.Pharm, or advanced degree in Life Sciences
  • Prior experience in CROs or pharmaceutical companies
  • Excellent scientific writing and grammar proficiency

Manager – Quality Assurance (QA)

Location: Pune / Hyderabad
Experience Required: 5–6 years

Key Responsibilities:

  • Oversee GCP audits, SOP reviews, and CAPA management
  • Coordinate internal and external site/vendor audits
  • Maintain high standards in documentation and regulatory compliance

Preferred Qualifications:

  • Degree in Life Sciences, Quality Management, or related field
  • Experience in CRO/Pharma QA functions
  • Knowledge of global QA practices and regulatory inspection preparedness

How to Apply:
Interested candidates are requested to share their updated CVs with the subject line indicating the “Position Title – Location” to:
hr@ardent-cro.com

Take the next step in your clinical research career with a trusted CRO known for quality, integrity, and innovation.


Educational Background Relevant for These Roles:

Life Sciences, Clinical Research, Pharmacy, Biotechnology, Chemistry, Medicine (MBBS/MD for other roles)


Quick Summary Table for SEO Optimization

Company NameCurrent VacanciesRequired EducationExperience Required
Ardent CROClinical Research Associate, Medical Writer, QA ManagerLife Sciences, Pharmacy, Clinical Research2–6 years
Ardent CRO Hiring Clinical Research Associate, Medical Writer, QA Manager
Ardent CRO Hiring Clinical Research Associate, Medical Writer, QA Manager
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