Clinical Research Jobs at Parexel | Apply Now For Clinical Research Associate Role
Parexel is inviting applications for the Clinical Research Associate II position in Bengaluru—an exceptional opportunity for professionals seeking advanced clinical research jobs in global clinical operations. This role is ideal for candidates aiming to grow as a Clinical Research Associate while contributing to high-impact studies across multiple therapeutic areas. If you’re looking for a rewarding Parexel career with international exposure, site monitoring responsibilities, and a strong focus on patient safety, this opening is a perfect fit.
- Job Position: Clinical Research Associate II
- Location: Bengaluru, India
- Job ID: R0000036743
- Job Category: Clinical Trials
About The Company
Parexel is a global leader in clinical research, helping accelerate the development of therapies that improve patient lives. A Parexel career offers the chance to work across diverse therapeutic areas, collaborate with world-class experts, and contribute to transformational healthcare research. As one of the most trusted names in clinical development, Parexel empowers Clinical Research Associates to grow, lead, and innovate.
Role Overview
As a Clinical Research Associate, you will serve as the primary point of contact for investigator sites and be fully accountable for site performance from initiation to close-out. Your role ensures participant safety, protocol adherence, regulatory compliance, and the overall quality of trial conduct. This opportunity is ideal for candidates aspiring to excel in clinical research jobs within a global clinical environment.
Key Responsibilities
- Manage product registration data in alignment with SOPs, Work Instructions, and global regulatory requirements.
- Extract and interpret data from regulatory dossiers; ensure accuracy, completeness, and compliance.
- Execute hands-on data management tasks, including updates, validation, workflow handling, and system entries.
- Perform QC checks to maintain data integrity across Teva’s Global Registration database.
- Support regulatory data–related projects, system integrations, and process improvements.
- Build strong working relationships with cross-functional and global regulatory teams.
- Contribute SME insights for current and future regulatory data systems.
Education
- Degree in Biological Sciences, or other health-related discipline.
- Equivalent clinical research experience may also be considered.
Skills & Job Knowledge
- Required
- Strong interest and aptitude in regulatory affairs and regulatory data management.
- Ability to interpret regulatory dossiers and understand registration data structures/workflows.
- Accuracy, attention to detail, and strong documentation habits.
- Good communication and stakeholder-management skills.
- Preferred
- Experience in pharmaceutical regulatory affairs or regulatory operations.
- Familiarity with regulatory information management systems (RIMS).
- Hands-on experience managing registration data in pharma environments.
Why Choose a Parexel Career?
Choosing a Parexel career means joining a mission-driven global organization dedicated to accelerating medical innovation. With structured growth pathways, extensive learning resources, and a collaborative environment, this opportunity helps you build a strong future in clinical research jobs and clinical operations.
