Principal Clinical Research Scientist at Johnson & Johnson leading clinical research for vision treatments. Engaging with cross-functional teams and contributing to regulatory strategies.
Responsibilities
Represent Clinical Science as core team member on critical projects, liaising between project and functional teams, and coordinating with Clinical Operations and Project Management partners to deliver on time, within budget, and in compliance with regulations and SOPs.
Activate and build collaborative relationships across business platforms as well as key cross-functional partners (e.g., Global Strategic Marketing, Medical Affairs, Regulatory Affairs, R&D, etc.) to ensure consistent alignment in new product development and through product life cycle.
Lead initiatives for appropriate interpretation and dissemination of all evidence generated, including Clinical Study Reports, abstracts, manuscripts, and MDR-related documents (CER, PMCF, Clinical Plans, etc.).
Contribute to clinical scientific discussions with regulatory agencies that support the clinical and regulatory strategy, including proposed investigations, review process of evidence to support marketing authorization, and support of regulatory inspections.
Engage and collaborate with industry's key opinion leaders, including KOLs and regulatory agencies, and build on relationships established through professional/technical societies.
Performs other related duties as assigned by management.
Requirements
An advanced degree in a Scientific Field is required.
A Doctoral Degree-Optometry or MD with specialty in Ophthalmology is highly recommended.
Minimum of 8 years of relevant clinical / scientific work experience, including leadership functions (ie. leading or mentoring teams, non-managerial leadership experiences) is required.
Experience in software-driven medical devices and capital equipment is preferred.
Strong technical writing ability, such as clinical study protocols, reports and abstracts is required.
Understanding of biostatistics as applied to study data is required.
Proficient with computers and software programs is required.
Ability to travel 10% of the time is required.
Benefits
Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits: Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period
10 days Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year
Job title
Principal Clinical Research Scientist – Equipment Platform Vision
Clinical Research Fellow conducting clinical research in cardiothoracic surgery and cardiovascular disease at Emory University. This fellowship offers comprehensive training and mentorship in clinical research methodology.
Clinical Research Nurse providing nursing support for research trials at Emory University. Involves clinical patient contact and participation in research studies at School of Medicine.
Lead biostatistician consulting on clinical research studies at Winship Cancer Institute. Requires expertise in R, SAS, and statistical analysis with extensive experience.
Senior Principal Scientist managing clinical research activities involving investigational compounds in Immunology. Focusing on late - stage development and comprehensive clinical trial management.
Clinical Research Coordinator II coordinating research visits and participant eligibility for movement disorders and stroke studies. Involves regulatory compliance and data management.
Clinical Trial Manager overseeing global Phase 3 program for cardiovascular drug development. Responsible for regional study and vendor management while collaborating with clinical operations teams.
Clinical Research Nurse Supervisor leading coordination of clinical studies at the Perelman School of Medicine. Overseeing study conduct, compliance, and supervising clinical staff in a hybrid role.
Clinical Research Nurse coordinating complex clinical trials for RadOnc CRU at University of Pennsylvania. Responsible for patient care and collaboration with research team on clinical activities.
Clinical Research Coordinator managing complex clinical trials in the Neurosurgery department at University of Pennsylvania. Ensures compliance and promotes good clinical practice in research protocols with mentorship responsibilities.
Clinical Research Coordinator overseeing data collection and research tasks at University of Arkansas for Medical Sciences. Analyzing data and training staff in adherence to protocols and quality standards.