AccordPro is inviting applications for the position of Clinical Research Coordinator at its Vadapalani, Chennai office. This full-time opportunity is ideal for experienced professionals from B.Pharm, Life Sciences, Nursing, Biotechnology, and healthcare backgrounds looking to build a career in clinical research, clinical operations, protocol management, and healthcare documentation.

The role offers exposure to international clinical research projects, patient coordination, prior authorization processes, laboratory operations, regulatory documentation, and clinical compliance. If you have 3–5 years of experience in clinical research or healthcare operations, this is an excellent opportunity to advance your career.

Clinical Research Coordinator Job Overview

Key Responsibilities

The selected Clinical Research Coordinator will be responsible for:

• Managing clinical research protocols and study documentation
• Tracking protocol milestones, payments, and study timelines
• Identifying eligible patients for clinical research studies
• Processing Prior Authorization (PA) requests
• Reviewing medical records, ICD codes, and clinical documentation
• Coordinating peer-to-peer reviews with healthcare providers
• Managing laboratory coordination and LabCorp follow-ups
• Monitoring clinical inventory and research supplies
• Assisting with literature reviews and monograph preparation
• Maintaining regulatory documentation and research compliance
• Ensuring HIPAA compliance throughout study activities
• Preparing operational reports and issue trackers
• Coordinating with vendors and internal healthcare teams

Educational Qualification

Candidates should possess any one of the following qualifications:

• Bachelor of Pharmacy (B.Pharm)
• Life Sciences
• Nursing
• Biotechnology
• Other Healthcare-related Bachelor’s Degree

Preferred:

• M.Pharm
• PhD in Pharmacy

Experience Required

Applicants should have 3–5 years of experience in one or more of the following:

• Clinical Research
• Clinical Operations
• Healthcare Operations
• Prior Authorization
• Medical Billing
• Clinical Documentation
• Healthcare Process Management

Preferred Skills

Successful candidates should have knowledge of:

• Clinical Research Coordination
• Clinical Trial Management
• Protocol Management
• Prior Authorization
• Clinical Documentation Review
• ICD Coding
• Healthcare Operations
• HIPAA Compliance
• Inventory Management
• Research Documentation
• MS Excel & MS Office
• Reporting & Data Analysis
• Stakeholder Communication

Why Join AccordPro?

Working at AccordPro provides professionals with:

• Opportunity to work with global clinical research teams
• International healthcare project exposure
• Strong career growth opportunities
• Learning-focused work culture
• Professional clinical operations environment
• Experience in global healthcare processes

How to Apply

Interested candidates should apply with their updated resume.

HR Contact: Prem
Phone: 9003756326

Application Link