Clinical Development Scientist

Job Title

Clinical Development Scientist

Job Description

Clinical Development Scientist

In this critical role, you will be supporting ongoing activities and accountability for clinical evidence strategy development, delivery & dissemination throughout the entire product creation and life-cycle to deliver evidence of value. Your role will execute on clinical and economic evidence related to the end to end (E2E) development process from ideation through post-market for Structural Heart/Heart Rhythm Management products.

Your role: 

• Executes clinical evidence activities through product development life cycle for products in our Structural Heart/heart rhythm management portfolio. Develops and authors clinical trial design, including scientific justification and guidance for analyses plans.
• Works with cross-functional teams to ensure that clinical data will support business needs, product claims, reimbursement, health economic outcomes and/or market access strategies. Contributes to accurate interpretation and appropriate dissemination of clinical evidence through authoring of clinical study reports, clinical evaluation reports, abstracts, podium presentations and peer reviewed manuscripts as assigned.
• Collaborate closely with external stakeholders including key opinion leaders and Investigators. Provides support for clinical evidence discussions with regulatory agencies, notified bodies, and physician advisory boards.
• Communicates across all levels of the organization and needs to be able to develop a rapport with indirect or functional leaders to influence decision-making and facilitating change.
• Fosters a successful team environment and adapts to changing priorities.

You're the right fit if:  

• You’ve acquired 3+ years scientific/research background with experience in clinical research.

• Your skills include medical writing experience, experience in the conduct of literature searches, effective verbal communication and presentation skills.

• You have a Bachelor’s Degree, required; PhD or MD preferred with a background in medical device design and/or Structural Heart procedures will substitute for 2 years of experience, preferred. Training and degree in science, engineering, or a medical field, required.

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.

• You also should possess knowledge of clinical research, device development processes, regulatory requirements, good clinical and data management practices.

• Must be able/willing to travel around 25% of the time.

How we work together

We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.

This is an office role.

About Philips

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