Clinical Research Associate Jobs at Ardent CRO in India with 2–5 years monitoring experience travel-based role competitive salary apply now
About the Company
Ardent CRO is an emerging Contract Research Organization delivering comprehensive clinical operations support across Phase I–IV clinical trials and BA/BE studies. The organization partners with sponsors, investigators, and regulatory authorities to ensure studies are conducted with scientific rigor, ethical integrity, and strict adherence to global regulatory standards.
With a strong focus on patient safety, data quality, and regulatory compliance, Ardent CRO supports pharmaceutical, biotechnology, and life sciences companies in accelerating the development of safe and effective therapies.
Job Details
- Job Title: Clinical Research Associate (CRA)
- Experience Required: 2–5 Years
- Employment Type: Full-Time
- Job Location: India (Travel-based role)
- Industry: Clinical Research / CRO / Life Sciences
- Vacancies: Multiple
Job Description
Ardent CRO is hiring experienced Clinical Research Associates to support monitoring activities across Phase I–IV clinical trials and BA/BE studies. This role is ideal for professionals with strong site monitoring experience, a solid understanding of ICH-GCP guidelines, and the ability to manage multiple trial sites independently. Clinical Research Associate Jobs
The position offers exposure to end-to-end clinical trial execution, working closely with investigators, sponsors, and internal teams to ensure protocol compliance, patient safety, and high-quality clinical data. Clinical Research Associate Jobs
Skills/Qualifications
Educational Background
Candidates should hold a degree in life sciences or healthcare-related disciplines. Eligible qualifications include:
- B.Pharm
- M.Pharm
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Clinical Research
- Pharmacy
- Nursing
- Allied Health Sciences
Experience Requirements
- Minimum 2 to 5 years of hands-on experience as a Clinical Research Associate
- Monitoring experience across Phase I–IV clinical trials and/or BA/BE studies
- Strong working knowledge of ICH-GCP, regulatory guidelines, and clinical trial SOPs
- Experience in site management, documentation review, and source data verification
- Willingness and ability to travel for on-site monitoring activities
Clinical Research Associate Jobs
Key Responsibilities
- Perform on-site, remote, and hybrid monitoring visits as per monitoring plans
- Ensure protocol adherence, patient safety, and data integrity at trial sites
- Monitor clinical trials across Phase I–IV and BA/BE studies
- Review informed consent processes and source documentation
- Verify CRF data against source documents and resolve discrepancies
- Identify, document, and follow up on protocol deviations
- Support site initiation, routine monitoring, and close-out visits
- Maintain Trial Master File (TMF) and essential site documents
- Train site staff on protocol requirements, GCP, and study procedures
- Communicate effectively with investigators, sponsors, and internal teams
- Prepare monitoring visit reports and follow-up letters within defined timelines
Clinical Research Associate Jobs
Benefits/Perks
- Competitive salary aligned with industry standards
- Exposure to global clinical trials and multiple study phases
- Opportunity to work in a quality-driven and compliance-focused CRO
- Professional growth through diverse therapeutic area exposure
- Hands-on involvement in end-to-end clinical trial operations
Clinical Research Associate Jobs
Why You Should Join
- Work on Phase I–IV clinical trials and BA/BE studies
- Enhance expertise in site monitoring and regulatory compliance
- Gain experience with diverse sponsors and therapeutic areas
- Be part of a growing CRO focused on quality and patient safety
- Build a strong long-term career in clinical research operations
Clinical Research Associate Jobs
Frequently Asked Questions (FAQs)
Is this role open to candidates with only BA/BE experience?
Yes. Candidates with BA/BE monitoring experience are encouraged to apply.
Does this position require travel?
Yes. This is a travel-based role and requires visits to clinical trial sites.
Is remote monitoring experience acceptable?
Yes. Experience in on-site, remote, or hybrid monitoring models is acceptable.
Which therapeutic areas are involved?
Multiple therapeutic areas may be involved depending on sponsor and study requirements.
Is ICH-GCP certification mandatory?
Strong working knowledge of ICH-GCP is mandatory; certification is preferred.
How to Apply
Interested and eligible candidates should apply by sharing their updated resume via email.
Email: hr@ardent-cro.com
Shortlisted candidates will be contacted for further discussion and interview rounds.
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