Clinical Research Associate Jobs at Parexel: iCRA II Role | Life Sciences Jobs | Apply Now
Are you searching for Clinical Research Associate Jobs that combine strategy, regulatory expertise, and global clinical exposure? Parexel Careers brings an exciting iCRA II opportunity for professionals aiming to grow through impactful Life Sciences Jobs. This role focuses on study start-up, site activation, and regulatory submissions while supporting complex global clinical trials.
- Position: iCRA II
- Primary Location: India, Bengaluru
- Job ID: R0000036655
- Category: Clinical Trials
About the Company:
Parexel is a leading global clinical research organization committed to improving patient outcomes through innovative research and regulatory excellence. Through Parexel Careers, professionals gain access to purpose-driven Life Sciences Jobs that support pharmaceutical and biotechnology advancements worldwide.
Job Overview:
The iCRA II role is responsible for managing and driving start-up, Pre-SIV, and activation activities for clinical studies. This position supports protocol amendment submissions, regulatory approvals, essential document review, and site readiness. The role requires close collaboration with investigators, sponsors, and internal teams to ensure timely site activation and compliance with regulatory standards.
Key Responsibilities:
- Act as Parexel’s primary point of contact for assigned clinical sites
- Manage site start-up activities from identification through activation
- Prepare, review, and submit IRB/IEC and regulatory applications
- Customize and negotiate informed consent documents and amendments
- Ensure timely submission and quality of Trial Master File documentation
- Maintain accurate updates in Clinical Trial Management Systems
- Identify, resolve, or escalate site risks and activation challenges
- Support audit and inspection readiness for assigned sites
Educational Requirements:
- Degree in biological sciences, related discipline or equivalent clinical research experience
Skills Required:
- Strong understanding of clinical trial methodology and regulations
- Knowledge of ICH-GCP and regulatory compliance
- Excellent analytical, organizational, and problem-solving skills
- Strong communication and stakeholder management abilities
- Experience with CTMS, eTMF, and clinical documentation systems
- Ability to work independently in a matrix and global environment
If you are aiming to advance your career through challenging Clinical Research Associate Jobs, this iCRA II role via Parexel Careers offers global exposure, professional growth, and long-term stability within high-impact Life Sciences Jobs.
