Parexel CRA Job | Clinical Research Associate in Bengaluru | Apply Now!
Join Parexel, a global leader in clinical research and drug development, as a Clinical Research Associate II (CRA II) in Bengaluru, India. In this role, you will be responsible for ensuring patient safety, regulatory compliance, and high-quality clinical trials while working with investigators and research sites. If you have clinical research experience, a degree in biological sciences, pharmacy, or nursing, and a passion for advancing medical treatments, we want to hear from you!
About Parexel
Parexel is a leading global clinical research organization (CRO) dedicated to accelerating drug development and bringing life-changing treatments to patients worldwide. With over 40 years of experience, Parexel partners with pharmaceutical, biotechnology, and medical device companies to conduct high-quality clinical trials that ensure patient safety, regulatory compliance, and scientific excellence. Headquartered in Durham, North Carolina, USA, Parexel operates in more than 100 countries, offering full-service clinical trial management, regulatory consulting, and real-world evidence solutions. The company is known for its patient-first approach, innovative research methodologies, and commitment to improving healthcare outcomes.
About Parexel CRA II Job Role
Job Post: Clinical Research Associate II
Location: Bengaluru, India
Job ID: R0000031331
Category: Clinical Trials
Key Accountabilities
Start-up (from site identification through pre-initiation):
- Act as Parexel’s direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase.
- Build relationships with investigators and site staff.
- Conduct, drive, and manage country-specific feasibility and/or site pre-qualification and qualification activities.
Maintenance (from initiation through close out):
- Serve as the primary contact for assigned sites, ensuring compliance with Parexel CRA II job responsibilities.
- Facilitate and support site with access to relevant study systems and ensure sites are compliant with project-specific training requirements.
- Evaluate if on-site staff assignment is still accurate and implement corrective actions.
Overall Accountabilities from Site Identification to Close out:
- Ensure timely and accurate completion of project goals.
- Monitor and maintain compliance with ICH-GCP and applicable international and local regulations.
- Show commitment and perform consistent, high-quality work.
Skills for Parexel CRA II Job
- Problem-solving and analytical thinking
- Strong communication and interpersonal skills
- Advanced presentation and client engagement abilities
- Proficiency in clinical trial management systems and data analysis
- Ability to manage multiple priorities and meet project deadlines
Knowledge and Experience
- Prior site management experience or clinical research exposure.
- Familiarity with clinical trial methodology, GCP guidelines, and medical terminology
Education for Parexel CRA II Job
- Degree in Biological Sciences, Pharmacy, Nursing, or a related field.
- Equivalent experience in clinical research or site management is also considered.
Keywords: Parexel, Clinical Research Associate, CRA II, Clinical Trials, Clinical Research Organization, CRO, Drug Development, Patient Safety, Regulatory Compliance
