Clinical Development Scientist

Philips•San Diego, CA

2d•Onsite

About The Position

Clinical Development Scientist, Image Guided Therapy Devices The Clinical Development Scientist ensures clinical trial protocols and studies comply with regulatory standards and business strategies, producing thorough evaluation reports and regulatory submissions. This role analyzes and troubleshoots complex clinical data issues, supports evidence-based decision-making, and fosters innovation in study design and evidence generation.

Requirements

5+ years of experience of related experience.
Strong knowledge and understanding of evidence synthesis for the medical device industry (literature reviews, gap assessments, evidence roadmap, etc.).
Regulatory awareness in the US and EU.
Strong clinical research competency.
Bachelor’s/master’s degree in a life sciences, bioengineering, or integrated physiology field with related medical device clinical development experience.
Must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.
Excellent communicator, with an ability to influence cross-functional stakeholders utilizing your clinical expertise and knowledge of research standards and guidelines within the medical device industry.
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

Nice To Haves

Direct cardiovascular domain expertise strongly preferred.

Responsibilities

Reviews clinical trial protocols and studies to ensure compliance with regulatory standards.
Aligns clinical activities with business strategies and objectives.
Evaluates protocols and recommends improvements for greater effectiveness.
Identifies opportunities to optimize study designs and processes.
Provides actionable feedback to enhance clinical protocol quality and outcomes.