Staff Clinical Trial Specialist

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
Discovery & Pre-Clinical/Clinical Development

Job Sub Function:
Clinical Development & Research – Non-MD

Job Category:
Scientific/Technology

All Job Posting Locations:
Jacksonville, Florida, United States of America

Job Description:

We are searching for the best talent to join our Vision team as a Staff Clinical Trial Specialist located in Jacksonville, FL

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges.

Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.

Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.

Your unique talents will help patients on their journey to wellness.

Learn more at https://www.jnj.com/medtech

Purpose: The Staff Clinical Trials Specialist manages study conduct under the guidance of a senior level manager ensuring that operating procedures and company policies are followed.

The Staff Clinical Trial Specialist develops and manages timelines, resourcing, and budget for assigned clinical trials.

They build cross-functional support for innovative solutions and facilitate successful study team behavior.

They partner with Research & Development and Research Scientists/Clinicians to ensure study results and timelines are met.

They maintain relationships externally with strategic partners, monitors, Clinical Research Organizations, and study site investigators/personnel.

They adhere to environmental policy, procedures, and support department environmental objectives.

They engage in Credo-based decision-making where our responsibility is to our patients and doctors.

You will:


* Own processes and information required to complete and support the clinical trial including clinical trial project plan, project timelines, resourcing, budget plans, and statements of work


* Accountable for the preparation and finalization of key clinical documents which include the informed consent, case report forms, and other essential study documents


* Manage study conduct...