Parexel Hiring Clinical Research Associates – FSP

Parexel Hiring Clinical Research Associates – FSP | Apply Now!

Parexel, a globally recognized contract research organization (CRO), is looking for Clinical Research Associates (CRA) – FSP in Bengaluru, India. This is a fantastic opportunity for professionals passionate about clinical research and drug development. If you have a background in Life Sciences, Pharmacy, or Nursing, and experience in site management or clinical trials, this role could be the perfect fit for you!

About Parexel

Parexel is a leading clinical research organization dedicated to improving global health through innovative clinical solutions. With a strong presence worldwide, Parexel supports pharmaceutical, biotechnology, and medical device companies in bringing new treatments to market.

Job Overview

Job Title: Clinical Research Associate (CRA) – FSP
Location: Bengaluru, India
Department: Clinical Research
Employment Type: Full-time

Key Responsibilities

1. Clinical Site Management

• Serve as Parexel’s primary contact with assigned clinical trial sites.
• Ensure compliance with study protocols and regulatory requirements.
• Conduct site visits (initiation, monitoring, and close-out) and assess site performance.
• Build and maintain strong relationships with site staff and investigators.

2. Regulatory Compliance & Data Quality

• Ensure adherence to ICH-GCP guidelines and regulatory requirements.
• Monitor study data for accuracy, completeness, and consistency.
• Assist sites with training on study protocols, data collection, and compliance.
• Address any protocol deviations, compliance issues, and discrepancies in study data.

3. Risk-Based Monitoring & Patient Safety

• Identify and mitigate risks related to patient safety and trial compliance.
• Support site recruitment strategies to meet study targets.
• Ensure adverse events (AEs) and serious adverse events (SAEs) are reported promptly.

4. Documentation & Reporting

• Maintain essential documents in Trial Master File (TMF).
• Complete monitoring visit reports and site action plans.
• Assist with audits, inspections, and quality reviews.

Qualifications & Requirements

Educational Background

• Bachelor’s/Master’s degree in Life Sciences, Pharmacy (B Pharm, M.Pharm), Nursing (BSc Nursing, MSc Nursing), Biotechnology, Microbiology, or other health-related disciplines.

Experience Required

• 1-3 years of experience in clinical research, site monitoring, or regulatory compliance.
• Experience in handling clinical trial documentation, CTMS, EDC systems.
• Knowledge of GCP guidelines, ICH regulations, and clinical trial protocols.

Skills & Competencies

• Strong analytical and problem-solving skills.
• Excellent communication and interpersonal abilities.
• Ability to work independently and in a team.
• Proficiency in MS Office (Excel, Word, PowerPoint).
• Willingness to travel extensively for site visits.

How to Apply?

Interested candidates can apply directly through the Parexel Careers Portal by clicking the link below:
Apply Here

Job Summary Table

Company Name	Current Vacancies	Required Education	Experience Required	Location
Parexel	Clinical Research Associate (CRA) – FSP	B Pharm, M.Pharm, BSc/MSc Life Sciences, Nursing	1-3 years	Bengaluru, India