Clinical Development Scientist

Philips


Date: 3 weeks ago
City: Plymouth, MN
Contract type: Full time
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 Heart Rhythm Management/Structural Heart products.

Your role:
  • Executes clinical evidence activities through product development life cycle for products in 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 5+ years scientific/research background with experience in clinical research conduct including methodology and statistics.
  • Your skills include strong medical writing experience, effective verbal communication and presentation skills in technical/clinical applications and experience in the conduct of literature searches pertinent to clinical/medical research.
  • You have a PhD or MD 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.

About Philips

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

  • Learn more about our business.
  • Discover our rich and exciting history.
  • Learn more about our purpose.
  • Read more about our employee benefits.

If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

Additional Information

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.

You must reside in, be within commuting distance or be willing to relocate to Plymouth, MN.

This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.

Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.

How to apply

To apply for this job you need to authorize on our website. If you don't have an account yet, please register.

Post a resume

Similar jobs

Construction Safety and Quality Coordinator

Roers Companies, Plymouth, MN
5 days ago
DescriptionRoers Companies is seeking an energetic, dedicated professional to join our team in Minneapolis, MN, as a Construction Safety Coordinator!About UsRoers Companies is a 2024 USA Today Top Workplace and an emerging national leader in multifamily real estate investment, development, construction, and property management. Headquartered in Plymouth, Minnesota, we’re on a mission to elevate multifamily housing by developing and operating...

Field Scientist

Terracon, Plymouth, MN
2 weeks ago
Job DescriptionIf you are currently working in the environmental space and have an interest in asbestos, lead and industrial hygiene field, or if you looking to get into the environmental space and want to learn more about the industrial hygiene field, Terracon’s Minneapolis, MN office has and exciting opportunity for you! Terracon has been Ranked #1 for Asbestos and Lead...

Human Resources Business Partner

Roers Companies, Plymouth, MN
4 weeks ago
Description: About UsRoers Companies is a 2023 Star Tribune Top 200 Workplace and an emerging leader in real estate investment, development, construction, and property management. Headquartered in Plymouth, Minnesota, we're on a mission to elevate multifamily housing nationwide by developing and operating market-rate and affordable housing. Since our founding in 2012, our team has developed more than $2.5 billion in...