Navitas Life Sciences looking for passionate Life Sciences professionals for Senior Consultant- Regulatory Affairs department at US – Remote
Are you looking for a new career challenge? Look no further as we are seeking new personnel to join our growing team as we continue working to drive better outcomes for drug development. We have exciting opportunities available across the globe with a mix of office, remote, and hybrid working available.
Navitas Life Sciences is
HIRING!
We are looking for passionate Life Sciences professionals across the globe to join our team
Senior Consultant
Job Description:
We are currently seeking a Senior Consultant to join our growing team. This is a core role within the Navitas Life Sciences business, where you will focus on the successful delivery of consultancy projects, managing project workstreams and client relationships, as well as initiating business development activities. An example of job responsibilities include the following:
To independently lead workstreams or sub projects to build client solutions and ensure effective implementation of consultancy projects
To manage and own the implementation of projects elements or workstreams
To define and understand client needs and lead the analysis, design, and implementations of work stream solutions on projects
To anchor all outputs to agreed project scope, objectives, deliverables, and timelines
To perform routine project management, status reporting and stakeholder management
To proactively maintain significant client contact – face-to-face client dialogue, project team meetings, facilitate workshops to develop distinctive solutions, and effective client outcomes
To act as a Subject Matter Expert on client projects and/or Navitas Life Sciences industry-leading PV and Regulatory Networks
To coach other team members in the design of solutions, workshops and presentations
To produce ‘client ready’ versions of materials and presentations, which clearly answer the business need
To support business development activities to drive business growth
To identify business opportunities, identify leads and support routine client relationship management
To conduct and support new business development activities e.g. proposal development, RFPs
To contribute to routine account meetings to build and manage opportunities
To act as a valued member of Navitas Life Sciences and contribute to collateral development
To provide support and involvement in strategic themes and/or support management initiatives
To develop collateral for projects/domain areas e.g. case studies, PoV
To act as a SME to develop and deliver knowledge management and training tools and materials
Demonstrate appropriate professionalism, drive and responsibility for tasks and own development within Navitas Life Sciences
Desirable Skills and Experience
5 years in a Life Science industry or consulting role of which:
2 years in a Consulting role and/or
3 years in a Life Sciences/Pharma industry role
Experience in 1 of the following areas is preferred:
Patient Safety and Pharmacovigilance
Clinical Development Processes
Labelling, Regulatory Affairs
Risk Management, Quality and Compliance
Evidence of capability
Solid consulting skills – methodologies/tools
Confident and concise communication
Solid client and project management capability, to include:
Scoping and requirements definition
Business case development
Planning, scheduling, and tracking
Stakeholder management
Resource management
Status reporting – issue and risk management
Communication planning: reports, meetings
Implementation planning
Project close out
Commercial acumen and some business development experience
Personal Skills: Confidence, professionalism, self-starter, resilience, and social awareness
Location: US – Remote
Strong degree (2:1 in a relevant subject area (e.g. Science or industry related) PhD or MBA preferable
Position: Manager
Department: Regulatory Affairs
Work Type: Full Time