Job ID: 2025-4768 Type: Regular Full-Time # of Openings: 1 Category: Clinical & Regulatory US-CA-Redwood City, Remote
Overview
This position is responsible for defining clinical research strategies, goals, and objectives including small-scale feasibility studies, new indication clinical assessments, and post-market studies for claims generation and safety & efficacy confirmation. The position works cross-functionally to implement the defined plans using internal and external resources.
Job Responsibilities:
Assess clinical research opportunities (both Nevro-sponsored and Investigator Initiated) and recommend project to bring forward.
Develop and implement clinical study strategies with relevant executive staff, working in collaboration with regulatory affairs, marketing, research & development, reimbursement, and outcomes planning.
Manage team of clinical scientists to engage and collaborate with physicians/clinicians on design and implementation of feasibility, new indication, and post-market clinical studies.
Develop, review and approve protocols for projects, both sponsored and investigator-initiated.
Participates in site selection and qualification, reviewing investigational sites. Participates in site selection committee and advises on final selection.
Establish and maintain relationships with key KOLs.
Responsibility for preparation of clinical reports for regulatory and medical purposes, including presentation and publications.
Works with physicians and internal marketing team on the presentation/publication of clinical material.
Participates in the dissemination of clinical information to the clinical team members and extended core team members, as appropriate.
Communicate/educate as company expert for Nevro clinical research
Collaborate and educate clinical project/program managers and clinical operations staff
Other responsibilities as assigned
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Responsibilities
Degree in science/health/engineering (e.g., Electrical, Mechanical, and/or Biomedical Engineering) required. Master’s degree or PhD preferred.
5+ years experience in clinical/scientific research, medical devices/pharmaceutical clinical trials, plus 5+ years experience working with clinical professionals within a team, as well as working in a cross-functional product development setting.
Qualifications
Team Leadership: Ability to lead and motivate cross-functional teams, including clinical research associates, scientists, and support staff.
Clinical Trial Design: In-depth understanding of clinical trial methodologies, including protocol development and implementation.
Regulatory Knowledge: Familiarity with regulatory requirements (e.g., FDA, EMA) and guidelines (e.g., ICH-GCP) governing clinical trials.
Strategic Planning: Ability to develop and implement clinical research strategies that align with organizational goals.
Stakeholder Communication: Strong communication skills to liaise with internal teams, regulatory bodies, and external partners.
Resource Allocation: Expertise in allocating resources efficiently to optimize trial outcomes and cost-effectiveness.
Compliance Monitoring: Ability to ensure all research activities comply with regulatory and ethical standards.
Adaptability: Capable of adjusting strategies in response to changing conditions or unforeseen challenges.
Nevro offers equal employment opportunity, regardless of race, color, creed, religion, national origin, marital or family status, sex, sexual orientation, gender expression (including religious dress and grooming practices), gender (including pregnancy, childbirth or medical condition related to pregnancy or childbirth), physical or mental condition, disability, age or other characteristics protected by laws.
