Regulatory Affairs Manager.
2 weeks ago
Job Description
You will focus on leading regulatory services for global research projects of novel medicinal products in India while joining our global team of regulatory and ethics submissions experts. Join our team and contribute to groundbreaking clinical research.
Office-based in Bangalore or Remote in India
Oversee preparation of clinical trial submission dossiers for regulatory authorities in India, including Import and Export license applications Communicate with regulatory authorities, project teams and vendors on regulatory-related matters Develop and review project planning documents & processes, including study timelines for India Track changes/amendments to legislative acts pertaining to clinical trials in India and timely notification of all parties involved Develop and maintain regulatory requirements database Perform quality control of regulatory dossiers Ensures accurate and time-bound reporting of safety issues to local authorities Train PSI staff in regulatory aspects of clinical trials Mentor and train junior regulatory staff Participate in the regulatory aspects of feasibility research, support Business Development at client presentations and bid defense meetings
Qualifications
University degree 5 years of hands-on experience with clinical trial submissions (independent preparation of submissions dossiers for DCGI, including preparation of application forms, Executive Summary, country-specific statement, as well as country-level customization of patient documents) Extensive experience in regulatory aspects of clinical research with profound knowledge of regulations pertaining to clinical trials in India Full working proficiency in English Proficiency in MS Office applications Ability to learn, plan and work in a dynamic team environment Communication, collaboration, and problem-solving skills
Additional Information
You will work closely with driven and dedicated cross-functional teams, get all support and ownership of your projects.
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