Managing Consultant - Pharmacovigilance and/or Regulatory Labeling Life sciences – US (Remote Opportunity) Navitas Life Sciences is a global consulting and services organization operating in the life sciences sector. Our clients are leading life science organizations including those working in Pharmaceutical, Biotechnology, Consumer Health, Medical Devices, and Dietary Supplements. Growing demand requires the continuing expansion of our consulting team. Our current assignments focus on enhancing performance in a range of regulated business activities, including: Patient Safety and Pharmacovigilance Labeling and Regulatory Affairs Medical Governance, Quality and Compliance About the RoleWe are looking for a Managing Consultant with a track record of previous consulting experience in Regulatory affairs labeling projects and Pharmacovigilance/Safety to independently (a) lead work streams or subprojects to assess the client’s current Labeling/ PV management process, governance and technologies, (b) build suitable client solutions and (c) ensure effective implementation of developed solutions. Requirement: Lead a portfolio of complex consulting assignments to deliver innovative client solutionsLead the project delivery, multiple and /or complex projects, act as prime client contact Provide leadership, bring insight and gravitas to the analysis, design and implementation of projects Build executive level client and stakeholder relationships across projects and accounts Oversee effective project budgeting and financial controls to ensure profitability Provide thought leadership across Labelling/RA and/or PV solutions and services Bring latest thinking and insight to develop industry-leading RA / / PV / Labeling solutionsLead working groups, forums discussions and content development to support our industry networks Build industry presence, networks and drive business development Develop collateral for projects/domain areas e.g. author case studies, white papers, new concepts Be an integral part of the consulting leadership of NLS to build and grow the business Conduct business development activities tovv drive growth – build relationships, conduct meetings, build proposals, close successful negotiations to secure project and account expansion Lead and coach direct reports and project teams Lead strategic themes, internal projects and/or business improvement initiatives Lead company meeting sessions, enthusiastically acts as a role model The successful candidate will preferably have experience in: At least 8 years+ consulting expeirence - a blend of operating model, process and tehcnology conulting experience. Proven Management consulting skills to include: Program and Project management Process design analysis, design, implementation Business transformation / change management Governance and organizational design Technology landscape assessment / implementation Evidence of success with consulting methodologies Preferred experience in a regulatory or labeling role. Subject Matter Expertise in Regulatory Labeling and or PV Contextual understanding and experience in LS regulatory and/or PV Track record in driving growth. Digitally savvy, thirst to grow and succeed in an entrepreneurial environment
WHY NAVITAS INC?
here are many reasons why you would choose to continue your career at Navitas Life Sciences Great benefits, ample opportunities for growth and development, international opportunities, thechance to work on incredible projects with the best and brightest people, and more.
Note:
Navitas is hiring for Management consultant role for both Regulatory Labelling and Pharmacovigilance vertical for US and UK Location. What you see is a consolidated Job description. Please ask for the individual JD when you apply for the role. Strictly no agencies please** Job offer is subjected to successful interview completion and background check verification. Interested candidate: Please send your profiles to Recruitment.princeton@navitaslifesciences.com