Sr Analyst - Clinical Trial Coordinator

Job Summary

As a Clinical Trial Coordinator within the Local-Regional Studies Support Office, you will play a meaningful role in keeping global clinical trials on track - ensuring the operational backbone of each study runs with precision, compliance, and care. Working as part of dedicated trial teams across a broad portfolio of local and regional studies, you will coordinate and support a range of essential trial activities, from budget and invoice tracking to quality issue support and regulatory reporting oversight. Clear guidance from senior colleagues will support your growth as you contribute directly to the quality and integrity of clinical development operations.

Responsibilities

• Coordinate and support essential trial activities, including budget and invoice tracking.
• Provide quality issue support and regulatory reporting oversight across trials.

Location & Employment Type

Location: Bangalore, India | Hybrid | Full time.

Requirements

• A bachelor's degree or equivalent in a scientific field, with up to one year of experience in a clinical research-related role; candidates without a degree are welcome with a minimum of three years of relevant professional experience and additional qualifications demonstrating exposure to clinical research fundamentals.
• A foundational understanding of clinical operations and ICH-GCP guidelines, paired with comfort navigating the administrative and coordination demands of a clinical trial environment.
• Proficiency in standard office productivity tools - including spreadsheet, word processing, and presentation software - and some familiarity with clinical trial management systems.
• Clear and confident communication skills in English, both written and verbal, with the ability to exchange information effectively across functions and geographies.
• Strong organizational skills and a conscientious, detail-oriented approach - capable of managing high-volume tasks while maintaining quality and meeting deadlines in a structured, supervised environment.
• A collaborative mindset with the ability to work independently, and a genuine comfort operating within an international, multicultural matrix environment.
• A proactive attitude toward accountability and adaptability - willing to take on responsibility, ask questions, check for understanding, and continuously build expertise.

Skills

• Clinical operations
• ICH-GCP guidelines
• Clinical trial management systems
• Budget and invoice tracking
• Regulatory reporting
• Office productivity tools (spreadsheet, word processing, presentation software)
• English communication
• Strong organizational skills
• Attention to detail

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.