Provide active medical and scientific contribution to a matrixed cross-functional Compound Development Team and the Clinical Team
Team matrix interactions may include project management, finance, legal, quality assurance, quality monitoring & compliance, clinical supplies unit, TA strategy, regulatory affairs, data management, medical writing, biostatistics, global medical affairs, clinical pharmacology, clinical operations, health economics, epidemiology and other scientific and business-related disciplines
Lead the clinical team and be responsible for timely completion, content and quality of key documents e.g. clinical development plans, protocol development, execution of clinical studies, preparation of clinical study reports and for the preparation and approval of essential documents for regulatory filings
Working with functional partners responsible for the clinical development strategy for the assigned development program(s) and accountable for its execution
Providing leadership on managing/addressing specific project/program-related issues and presenting to and negotiating with the NS and Johnson and Johnson Innovative Medicine, Research & Development leadership teams on development plans or program-related issues
Working with global clinical operations, Regulatory, and Global Medical Safety, leads the clinical team in responding to medical and compound-related issues
Working with Regulatory Affairs and global clinical operations to respond to questions from Health Authorities and IRBs/ECs
Provides key input to statistical analysis plans and the interpretation of statistical analyses
Presenting and/or responding to questions at meetings with Health Authorities, including FDA advisory committee meetings and/or CHMP presentations
Provides key input into diligence activities
Supervises direct reports if assigned
Participates or leads cross-departmental or cross-functional projects with broad Johnson and Johnson Innovative Medicine impact
Builds professional relationships with opinion leaders, investigators and key regulatory officials
May act as company spokesperson regarding publication of research findings and presentations to relevant health authorities and consultant/advisory meetings
Requirements
MD (or equivalent) is required
Detailed and thorough understanding of neurodegenerative disorders including Parkinson’s disease is required
Requires at least 10 years of experience in clinical research and development
Experience interacting with global health authorities is strongly preferred (FDA, EMA etc)
Exceptional interpersonal and communication skills, with the ability to build strong relationships and influence without reporting authority
Excellent problem-solving and conflict resolution skills, with the ability to navigate complex and challenging situations
Up to 20% annual travel (domestic and international) may be required
Strategic mindset
Experience and interest in innovative clinical trial design
Fluent in written and spoken English
Working knowledge of the use of Microsoft suite of software products including Excel and Word
Experience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filings
Outstanding interpersonal and communication skills.
Experience in leading people (directly and in a matrix) of varying levels via coaching and open conversations to reach their full potential, while also providing support and guidance during periods of poor performance
Excellent problem solving and decision-making abilities.
Benefits
medical
dental
vision
life insurance
short
and long-term disability
business accident insurance
group legal insurance
retirement plan (pension)
savings plan (401(k))
long-term incentive program
Vacation –120 hours per calendar year
Sick time
40 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
Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member