Senior Principal - Research and Development, Life Sciences
Infosys Consulting is looking for talented and highly motivated consultants to join our Life Sciences consulting practice specializing in Regulatory Sub Practice of Larger Life Sciences Consulting.
RESPONSIBILITIES
- In depth knowledge of Pharma Regulatory Operations and Regulatory IT Systems aligned to core Functional and Technical competencies
- Expert in Regulatory area with ability to drive futuristic IT solutions and experience in client facing and agency thought leadership.
- Understanding and knowledge of processes related to health authority submissions, content authoring, labeling, lifecycle management of CMC, regulatory intelligence, and country-specific regulatory requirements - keenly aware of industry trends, needs and business requirements expected from clients
- Able to strategize and advise on the product roadmap and should work closely with the client in delivering solutions.
- An empathic people manager responsible to mentor and guide a team for progressive outcomes
- Lead strategic programs, manage program planning, execution and reporting; responsible for program resources, deliverables, quality, stakeholder communication, client buy-in, program risks, mitigations and budgets leading to successful program delivery.
Want more jobs like this?
Get jobs in Bridgewater, NJ delivered to your inbox every week.
- Lead in sales pursuits in collaboration with larger Infosys teams; lead the proposal development process; proposal content creation and client presentations.
- Develop solutions that enable adoption of digital capabilities for Life Sciences organizations. Participate in analyst meetings, industry speaking engagements, publish white papers/ viewpoints in leading industry journals.
- Participate in practice development activities; coach junior consultants; participate in consultant training processes.
- Ability to travel 4 days a week to multiple client locations.
- The candidate should have a rare blend of industry domain, process, technical and consulting skills. Consulting skills should entail client relationship management, effective executive communication, critical thinking in a consultative approach with our clients. Additional skills that are highly desirable include value realization, process re-engineering, design thinking and agile delivery experienced
- Should have a master's degree in Life Science, Medical or Related discipline. Masters in business administration would be an added advantage.
- Minimum 12-15 years' experience in Regulatory Strategy, Operations and Intelligence across Biopharma and Medical Devices.
- Deep understanding of RIM systems i.e., Veeva Vault, LIQUENT and publishing tools.
- Knowledge of regulatory IT systems landscape and implementation experience inclusive of integration and Migration aspects
- Forward thinking skills in reshaping patient support and market access agenda as it evolves.
- Thought leadership and critical problem solving skills
- Candidates authorized to work for any employer in US without employer-based visa sponsorship are welcome to apply. Infosys is unable to provide immigration sponsorship for this role at this time
Along with competitive pay, as a full-time Infosys employee you are also eligible for the following benefits :-
• Medical/Dental/Vision/Life Insurance
• Long-term/Short-term Disability
• Health and Dependent Care Reimbursement Accounts
• Insurance (Accident, Critical Illness, Hospital Indemnity, Legal)
• 401(k) plan and contributions dependent on salary level
• Paid holidays plus Paid Time Off