Instagram
youtube
Facebook

Clinical Research Associate – Ii

2-3 years
₹6 – ₹8.5 LPA
10 July 18, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Position: Clinical Research Associate – II
Experience Required: 2–3 years
Joining: Immediate

About ProRelix Research:
ProRelix Research is a dynamic and forward-thinking Contract Research Organization (CRO) committed to delivering excellence in clinical trials. With a focus on ethical standards, innovation, and global impact, we provide comprehensive research solutions that shape the future of healthcare.

Role Overview:
We are seeking a Clinical Research Associate – II with 2–3 years of hands-on experience in clinical monitoring. This role offers a unique opportunity to contribute to global clinical research projects while advancing your career in a fast-paced, growth-oriented environment.

Key Responsibilities:

  • Conduct site selection, initiation, routine monitoring, and close-out visits in accordance with ICH-GCP and study protocols.

  • Ensure accurate and timely data collection, source verification, and regulatory compliance.

  • Build and maintain strong working relationships with investigators, site personnel, and project stakeholders.

  • Proactively identify and resolve site-related issues to ensure study timelines are met.

  • Maintain essential study documents and generate comprehensive monitoring reports.

  • Collaborate with cross-functional teams to support study deliverables and reporting requirements.

Requirements:

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related discipline.

  • 2–3 years of experience in clinical research as a CRA.

  • In-depth understanding of clinical trial guidelines (ICH-GCP, local regulations).

  • Excellent communication, problem-solving, and organizational skills.

  • Flexibility to travel based on site and project requirements.

What We Offer:

  • A chance to work on diverse and impactful global trials.

  • A collaborative, mission-driven work environment.

  • Career advancement opportunities and professional growth.

  • Immediate joining with supportive onboarding.

How to Apply:
Interested candidates can email their resume to
career@prorelixresearch.com.

Estimated Salary: ₹6 – ₹8.5 LPA (based on current industry standards for CRA II roles in India)