Amaris Clinical Hiring 2026 | QA-RA / Senior Research Associate Jobs | Apply Now
Looking for a career in clinical research and regulatory affairs? Amaris Clinical (a division of Caplin Point Laboratories) is hiring for the role of Quality Assurance – RA / Senior Research Associate.
This is a great opportunity for candidates with 2–5 years of experience in clinical research, GCP/GLP compliance, and regulatory processes to work in a science-driven and compliance-focused environment.
About Amaris Clinical
Amaris Clinical, part of Caplin Point Laboratories, is known for its clinical research excellence, regulatory compliance, and global standards in drug development. The organization focuses on delivering high-quality clinical and research solutions.
Job Overview
- Company: Amaris Clinical (Caplin Point Laboratories)
- Role: QA-RA / Senior Research Associate
- Experience: 2 to 5 Years
- Open Positions: 2
- Qualification: B.Pharm / M.Pharm
- Industry: Clinical Research / Pharmaceutical
Roles & Responsibilities
- Ensure compliance with GCP and GLP regulatory requirements
- Conduct protocol review and Trial Master File (TMF) review
- Handle clinical trial processes such as screening, dosing, sample collection, and documentation
- Manage IP handling, sample shipment, and related records
- Perform SOP review and equipment qualification documentation
- Support calibration, maintenance data review, and compliance checks
Key Requirements
- Strong knowledge of GCP & GLP guidelines
- Ability to manage multiple tasks and lead clinical teams
- Excellent organizational and documentation skills
- Experience in clinical trial operations and regulatory compliance
Why Join Amaris Clinical?
- Work in a science-driven clinical research environment
- Exposure to global regulatory standards
- Opportunity to grow into senior clinical and RA roles
- Strong focus on quality, compliance, and integrity
How to Apply
📧 Send your updated CV to: hr@amarisclinical.com
FAQs
Q1: What is the required experience?
2 to 5 years in clinical research, QA, or regulatory affairs.
Q2: What qualifications are required?
B.Pharm or M.Pharm.
Q3: Is this a clinical or desk-based role?
It involves both clinical operations and documentation/regulatory work.
Q4: How many positions are open?
There are 2 openings.
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