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Clinical Research Coordinator (Crc)

Curaclin Research
Curaclin Research
1-2 years
Not Disclosed
Bhubaneswar, India
10 Feb. 24, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Clinical Research Coordinator (CRC) – Bhubaneswar, Odisha
Location: Bhubaneswar, Odisha, India
Employment Type: Full-Time
Experience Required: 1–2 Years
Qualification: Pharmacy or Life Sciences Background

Job Overview

A growing clinical research organization is seeking a dedicated Clinical Research Coordinator (CRC) to join its expanding team in Bhubaneswar, Odisha. This role is ideal for professionals with 1–2 years of clinical research experience who are looking to strengthen their expertise in clinical trial coordination and site management.

The Clinical Research Coordinator will play a key role in supporting clinical studies, ensuring protocol compliance, and maintaining high standards of data accuracy and regulatory adherence.

This opportunity is well-suited for candidates searching for Clinical Research Coordinator jobs in Odisha, CRC roles in Bhubaneswar, or entry-to-mid level clinical trial site positions in India.

Key Responsibilities

  • Coordinate and support clinical trial activities in accordance with approved protocols

  • Assist with patient screening, recruitment, and informed consent procedures

  • Maintain accurate and up-to-date study documentation, including source documents and case report forms (CRFs)

  • Ensure compliance with ICH-GCP guidelines and regulatory requirements

  • Liaise with investigators, sponsors, CROs, and site staff to facilitate smooth study conduct

  • Manage investigational product accountability and site records

  • Support monitoring visits, audits, and regulatory inspections

Required Qualifications

  • Bachelor’s degree in Pharmacy, Life Sciences, or a related field

  • 1–2 years of experience as a Clinical Research Coordinator or in clinical trial site operations

  • Strong understanding of ICH-GCP and clinical research regulations

  • Excellent organizational and documentation skills

  • Effective communication and stakeholder coordination abilities

Why Apply?

This role offers hands-on exposure to clinical trial management within a growing research organization. Professionals seeking CRC jobs in Bhubaneswar, clinical research site coordinator roles in Odisha, or career advancement in Indian clinical trials will find this position aligned with long-term growth in the pharmaceutical and life sciences industry.

Application Process

Interested candidates may share their updated CV at:
hr.curaclinresearch@gmail.com

Applications will be reviewed on an ongoing basis.