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In-House
Little Falls, NJ, United States
Senior Counsel, Research & Development, Corporate Law
Attorney
Company Review
Min 7 yrs required
Full-time
No
SEO friendly job title: Senior Counsel, Research & Development, Corporate Law H1: Senior Counsel, Research & Development, Corporate Law H2: Key Responsibilities and Qualifications Bold headlines: - Senior Counsel position for Genentech R&D Law Group - Seeking highly experienced R&D attorney for global strategies - Key responsibilities include providing legal advice and serving as lead counsel - Qualifications include JD, 7+ years of relevant legal experience, and knowledge of relevant laws and regulations - Salary range of $198,500 to $368,600 with additional benefits - Genentech is an equal opportunity employer with a focus on professional development and diversity. Bullet points: - Highly experienced R&D attorney sought for Senior Counsel position - Will provide legal support for global strategies and activities related to product research and development, digital health, and personalized healthcare - Responsibilities include providing legal advice to advance company's pipeline, serving as lead counsel for global development programs, and collaborating with internal and external stakeholders - Must have JD, 7+ years of relevant legal experience, and knowledge of relevant laws and regulations - Salary range of $198,500 to $368,600 with additional benefits - Genentech values professional development and diversity in the workplace.
Not applicable
Available, details provided at link
Not specified
Legal Advice, Education, Issue Resolution, Strategic Legal Advice, Business Strategy, Regulatory Compliance, Transactional Legal Support, Global Strategies, Product Research, Drug Development, Device Development, Digital Solutions, Research Privacy, Informed Consent, Biomarker Research, Genomic Research, Real World Data, Secondary Use of Research Data, Pre-approval Access, Expanded Access, Lead Counsel, Global Development Programs, Scientific Initiatives, External Collaborators, Pharmaceutical Manufacturers, Digital Developers, Device Developers, Academic Institutions, Research Collaborative Groups, Government Entities, Internal Collaboration, External Collaboration, Intellectual Property, Privacy, Product Attorneys, Business Leadership, Regulatory Experts, Ethics Experts, Legal Policy Committee, JD, Licensed Attorney, Good Standing, Global Working Hours, Human Subject Protection Laws, Federal Food, Drug and Cosmetic Act, Privacy Laws, Clinical Development Programs, Data Sharing Arrangements, Clinical Supply Arrangements, Companion Diagnostic Developments, Complex Research Collaborations, Creative Problem Solving, Growth Mindset, Medical Device R&D, Digital Health R&D, Influential Communication, Influencing Skills, Verbal Communication, Written Communication, Client Relations, Organizational Savvy, Multidisciplinary Collaboration, Global Collaboration, Agility, Prioritization, Teamwork, Independent Work, Scientific/Technical Knowledge, Comfort with Change, Self-Motivated, Judgment, Ethics, Solutions-Oriented, Proactive, Strategic Legal Advice.
JD required
Interested candidates should apply through the company's website and submit a resume and cover letter.
Qualification and Experience JD, licensed and in good standing to practice law in one or more jurisdictions, at least 7 years of recent relevant legal experience, ability to work global working hours, significant knowledge of human subject protection laws, Federal Food, Drug and Cosmetic Act, privacy laws, and other applicable federal and state laws related to pharmaceutical research and development, significant transactional experience in clinical development programs, data sharing arrangements, clinical supply arrangements, companion diagnostic developments, and complex research collaborations.
Legal
USD 198500 to 368600 Annually
Apr 18, 2024
Aug 01, 2024
Qualification and ExperienceJD, licensed and in good standing to practice law in one or more jurisdictions, at least 7 years of recent relevant legal experience, ability to work global working hours, significant knowledge of human subject protection laws, Federal Food, Drug and Cosmetic Act, privacy laws, and other applicable federal and state laws related to pharmaceutical research and development, significant transactional experience in clinical development programs, data sharing arrangements, clinical supply arrangements, companion diagnostic developments, and complex research collaborations.
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