Vice President, Technical – Medical Device Luminary
Location: United States of America, Remote
Job Type: Full-Time
About the Role:
Parexel is seeking a highly accomplished Vice President, Technical – Medical Devices to serve as a recognized luminary within the Regulatory Consulting Services (RCS) business. This role is ideal for individuals with a profound Health Authority background or advanced industry leadership in regulatory strategy and development related to medical devices, including combination products and in vitro diagnostics.
As a leader at Parexel, you will be instrumental in shaping regulatory solutions for clients across the globe, utilizing your scientific, technical, and strategic expertise. This is an opportunity to influence product lifecycle decisions, mentor emerging consultants, and guide innovations in regulatory consulting methodologies—all while working remotely within a collaborative, high-performance environment.
Key Responsibilities:
Project Execution:
Lead and contribute to regulatory consulting projects both independently and within multidisciplinary teams.
Oversee workload prioritization and issue resolution to meet project objectives and scope.
Deliver high-quality deliverables that align with client expectations and internal standards.
Mentor and guide junior colleagues, offering support on technical methodologies and best practices.
Manage financial aspects and reporting in coordination with Project Leaders.
Thought Leadership:
Deliver presentations and author publications within industry forums based on recognized subject matter expertise.
Represent Parexel on association boards, advisory panels, and regulatory task forces.
Contribute to internal knowledge-sharing and innovation in consulting models and services.
Consulting and Client Management:
Serve as a trusted regulatory advisor to executive-level client stakeholders.
Customize consulting methodologies to fit client-specific needs, offering strategic insights and solutions.
Drive client satisfaction and business growth through relationship management and quality service delivery.
Identify and act on opportunities for follow-up business or scope expansion.
Required Qualifications:
Education: PhD required.
Experience: 15+ years of experience in regulatory strategy, medical devices, or combination product development.
Proven track record of regulatory expertise with key authorities (e.g., FDA, MHRA); previous Health Authority experience strongly preferred.
Recognized thought leader with contributions to publications, conferences, or professional associations.
Exceptional interpersonal skills with proven ability to advise at C-suite level.
Availability to travel up to 20–30% domestically and/or internationally.
Preferred Attributes:
Recognized industry authority with established relationships across regulatory networks.
Experience in developing new consulting models or methodologies.
Ability to serve in “loaned executive” capacities to client organizations.
Strategic thinker with deep knowledge of evolving regulatory environments.
Work Environment:
Remote-based with flexible scheduling.
Collaborative and innovative consulting culture.
Opportunities for continuous learning and advancement.
Equal Employment Opportunity:
Parexel is committed to providing equal employment opportunities for all individuals regardless of race, gender, age, disability, or veteran status.
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