Take your career to the next level and be involved in study startup processes in India. You will provide operational support to project teams and ensure that PSI clinical projects start smoothly and on time.
Office-based (Bangalore)
You will
- Develop site-specific startup timelines and meet the site activation targets
- Provide progress updates on the selected assigned projects and regular updates to all functions concerned
- Collect, review, and submit documents for ethics and regulatory review and approval (including review of study specific translations)
- Facilitate site budgets and contract negotiations
- Prepare packages of site documents for drug release to clinical sites
- Maintain study-specific and corporate startup tracking and filing systems
- MD, PharmD, RN or university/college degree in life sciences or an equivalent combination of education, training, and experience
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Practical Clinical Trial startup experience with clinical sites in India (regulatory submissions and/or contract and budget negotiation experience) is required
- Full working proficiency in English
- Excellent communication and organizational skills
- Ability to negotiate and build relationships at all levels
If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. Advance your career in clinical research and develop new skillsets whilst growing with the organization!
