5.0 - 8.0 years

8 - 13 Lacs

Bengaluru, Karnataka, India

On-site

Key Qualifications and Experience: Over 10 years of relevant experience in Clinical Trial Regulatory Submissions. Proven track record in managing clinical trial studies and serving as a Regulatory Lead for global trials, with specific exposure to the European market. Expertise in handling the CTIS database and submitting under EU CTR is highly desirable. Provides expert guidance to project team members. Works within broad project guidelines, facilitating issue and conflict resolution. Prioritizes personal workload and may prioritize the project teams workload to achieve project scope and objectives. Seizes opportunities to enhance project efficiency, results, or team performance and proactiv...

Posted 1 month ago

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