Principal Clinical Research Scientist

6 days ago

Jacksonville, United States Provident Research Inc Full time
Job DescriptionJob Description

Principal Clinical Research Scientist – Vision Care

With the global population aging and the demand for innovative vision care solutions on the rise, this role offers the opportunity to lead the translation of cutting-edge ophthalmic clinical research into life-changing products for millions of patients worldwide.

As the Principal Clinical Research Scientist, you will be at the forefront of my client’s mission to advance ophthalmic devices. Primarily responsible for partnering with the R&D team to design and develop clinical trial strategies, this role is suited for an experienced clinical development professional eager to engage in a strategic and impactful position. The successful candidate will have a strong background in clinical research and project management, ensuring that clinical trials are meticulously planned and executed, adhering to regulatory standards and timelines.

MUST BE ABLE TO BE IN-OFFICE 3 DAYS PER WEEK. THIS IS NOT A REMOTE ROLE.

Key Responsibilities:

  • Strategic Clinical Leadership: Develop and implement global evidence generation and dissemination strategies to support New Product Development (NPD) and Life-Cycle Management (LCM) projects, ensuring cross-functional collaboration and alignment.
  • Clinical Trial Design: Lead the design of clinical trials, ensuring they meet NPD/LCM needs and comply with global regulatory standards, while driving forward innovative ophthalmic solutions.
  • Evidence Dissemination: Oversee the interpretation and dissemination of clinical evidence through clinical study reports, scientific publications, and regulatory submissions, ensuring timely and impactful communication.
  • Stakeholder Engagement: Collaborate closely with key opinion leaders, regulatory bodies, and internal teams to shape clinical and regulatory strategies that support market access and reimbursement.
  • Project Management: Ensure the successful delivery of clinical projects on time and within budget, fostering strong partnerships with Clinical Operations and other key teams to achieve critical project milestones.
  • Continuous Improvement: Lead initiatives to enhance clinical processes and ensure ongoing compliance with industry regulations and internal policies.

Qualifications:

  • A Bachelor’s degree in Biological Science or a related discipline is required; an advanced degree in Ophthalmology, Optometry, or a PhD in a related field is preferred.
  • A minimum of 8 years of relevant scientific or technical experience, including leadership roles within Clinical Research.
  • Demonstrated expertise in clinical research science, product development processes, and global clinical trial regulations.
  • Proven ability to manage and deliver complex clinical programs, with a focus on driving innovation in ophthalmic care.
  • Strong leadership and collaboration skills, with the ability to influence and shape strategies across multidisciplinary teams.
  • Experience in engaging with regulatory agencies and external stakeholders to support clinical and regulatory strategies.

Working within a well-funded and rapidly advancing ophthalmic R&D pipeline, you’ll be empowered to deliver meaningful outcomes that improve the lives of patients globally.

 

Location Irvine, CA

Company DescriptionPRI is dedicated to providing our employees with the tools to succeed. Come and join the movementCompany DescriptionPRI is dedicated to providing our employees with the tools to succeed. Come and join the movement

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