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BioRadius is Hiring for Senior Clinical Research Associate (CRA)

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BioRadius Therapeutic Research is inviting applications for the position of Senior Clinical Research Associate (CRA) in the bioequivalence (BA/BE) studies domain. This opportunity is ideal for experienced clinical research professionals looking to grow into senior roles within CROs and pharmaceutical research organizations. With multiple openings available, candidates can expect exposure to high-quality clinical trial processes and regulatory frameworks.

Company Overview

BioRadius Therapeutic Research is a growing clinical research organization specializing in bioequivalence and bioavailability studies. The company supports pharmaceutical companies in conducting clinical trials, ensuring regulatory compliance, and maintaining data integrity for generic drug development.

With a strong emphasis on quality, compliance, and scientific accuracy, BioRadius provides a dynamic environment for professionals to build expertise in clinical operations and regulatory standards.

Job Role & Responsibilities

As a Senior Clinical Research Associate (CRA), you will play a key role in monitoring and managing clinical trials while ensuring adherence to regulatory standards.

Key Responsibilities

  • Monitor clinical trials in compliance with protocols, GCP, and regulatory guidelines
  • Conduct site visits, audits, and ensure proper trial execution
  • Review clinical data for accuracy, completeness, and ALCOA compliance
  • Coordinate with investigators, site staff, and internal teams
  • Prepare and review clinical trial documents and reports
  • Ensure documentation aligns with GDP standards
  • Identify and resolve issues related to study conduct and data quality
  • Mentor junior CRAs and support team development
  • Assist in regulatory submissions and inspections

Eligibility & Qualifications

Candidates must have one of the following qualifications:

  • B.Pharm, M.Pharm, Pharm.D
  • BSc / MSc in Life Sciences
  • Biotechnology, Clinical Research, Biochemistry, Microbiology

Required Skills

  • Strong understanding of GCP, GDP, and ALCOA principles
  • Knowledge of regulatory guidelines and clinical trial processes
  • Excellent documentation and reporting skills
  • High attention to detail and analytical thinking
  • Strong communication and coordination skills

Experience

  • 3 to 5 years of experience as a CRA in BA/BE studies

Salary & Benefits

  • Competitive salary based on industry standards
  • Estimated range: ₹5.5 LPA – ₹9 LPA
  • Opportunity to work in regulated clinical research environments
  • Career growth into senior and leadership roles
  • Exposure to regulatory audits and global standards

Job Location

  • India (exact location not specified)

How to Apply

Interested candidates can apply using the details below:

Candidates are encouraged to apply early due to limited openings.

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