Clinical Research Associate Job at Parexel | Biological Sciences | Apply Now
Parexel, a global leader in clinical research, is currently seeking an Initiation Clinical Research Associate (iCRA II) for its Bengaluru, India office. In this specialized Clinical Research Associate Job, you serve as the critical engine driving the “Start-up” phase of global clinical trials. Your primary mission is to manage the strategy for Pre-SIV (Site Initiation Visit) and activation tasks, ensuring that life-saving treatments reach patients as quickly and safely as possible. If you are looking to advance a Parexel Career within the Biological Sciences, this role offers a high-stakes, results-oriented environment where integrity and patient well-being are the top priorities.
- Job Position: iCRA II
- Location: India, Bengaluru
- Job ID R0000036655
- Category Clinical Trials
About The Company
Parexel is a leading global clinical research organization (CRO) dedicated to accelerating the development of innovative treatments to improve world health. As a core mission, Parexel acts as an integral link in the healthcare chain, ensuring that life-saving therapies reach patients sooner while maintaining the highest standards of safety and well-being. For those pursuing a Parexel Career, the company provides a platform to work on complex, global projects across a vast array of therapeutic areas.
Key Accountabilities
In this Biological Sciences Job, your success is measured by the speed and quality of site readiness.
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Regulatory Submissions: You prepare and submit IRB/IEC and MoH/RA applications, resolving conflicts and following up until final approval is received.
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Document Negotiation: You customize, review, and negotiate site-specific Informed Consent Forms (ICF) and translations.
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TMF Quality: You manage country and site-level Trial Master File (TMF) issues, ensuring “First Time Quality” (FTQ) for all essential documents.
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Systems Management: You maintain and update Clinical Trial Management Systems (CTMS) and ensure sites are compliant with project-specific training requirements.
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Risk Mitigation: You use judgment to resolve or escalate risks related to activation timelines, recruitment strategies, or study non-compliance.
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Inspection Readiness: You ensure that all assigned sites are audit and inspection-ready at all times, maintaining strict compliance with ICH-GCP guidelines.
Qualification and Experience
To excel in this Clinical Research Associate Job, Parexel looks for a combination of technical expertise and specific soft skills.
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Education: You should be educated to degree level in biological science.
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Experience: Substantial start-up experience or equivalent clinical research experience is required, alongside a deep understanding of clinical trials methodology and terminology.
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Technical Proficiency: Strong computer skills are essential, specifically with CTMS, eTMF, and Microsoft Office products.
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Interpersonal Traits: The “Success Profile” for this role includes being a problem-solver, a self-starter, detail-oriented, and a professional communicator.
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Matrix Environment: You must be willing to work in a matrix environment, valuing teamwork and the ability to prioritize multiple tasks autonomously.
In summary, the iCRA II position is a definitive Clinical Research Associate Job for those who thrive in the high-pressure, high-reward phase of study initiation. Choosing a Parexel Career means joining a team dedicated to efficiency and integrity, where you are encouraged to be inquisitive and take full accountability for project milestones. Because this Biological Sciences Job bridges the gap between site identification and the first patient visit, your expertise in regulatory submissions and site relationship management will be the cornerstone of the study’s success. If you are ready to be the catalyst that gets treatments to patients sooner, Parexel’s Bengaluru team is waiting for your application.
