Company

Bristol-Myers Squibb CompanySee more

addressAddressCambridge, MA
type Form of workFull-Time

Job description

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.
Paralegal Responsibilities
  • Advanced knowledge of US and foreign patent procedures M
  • Monitors progress of patent cases and patent attorney/agent dockets through use of USPTO Private PAIR, IP Management Software and Document Management System and seeks to reconcile any noted discrepancies.
  • Demonstrated efficient workload prioritization including the ability to efficiently manage multiple heavy dockets, multiple tasks, and e-mail workload including outside counsel e-mail review.
  • Reviews patent application files to check for compliance with USPTO requirements and BMS department standards, takes initiative to resolve discrepancies.
  • Reviews correspondence received from U.S. outside counsel law firms and expertly liaises with agents to ensure they are in compliance with BMS processes and procedures and USPTO rules and provides them with instructions and guidance in order to meet compliance.
  • Expert knowledge and working experience of the USPTO Patent Center filing system in order to independently draft and prepare simple to moderately complex patent legal documents for submission to the USPTO including (but not limited to) patent applications, figures, sequence listings, amendments, information disclosure statements, office action responses, requests for continued examination, notices of appeal, reply briefs, Allowance Checklists, Allowed Claims, issue fee payments ,etc.
  • Knowledge and expertise to customize/suggest language changes on forms as applicable to specific patent prosecution need.
  • Identifies patent legal issues and/or problems based on knowledge of PTO procedures and suggests and/or takes initiative to resolve.
  • Advanced skills to independently draft and assist with attorney responses to worldwide foreign patent agents.
  • Expert use and application of the Code of Federal Regulations (Title 37) and the Manual of Patent Examining Procedure (MPEP) to enable ability to identify legal issues/problems based on knowledge of PTO procedures.
  • Proficiently performs Patent Term Adjustment review and analysis and delivery of analysis summary to patent attorney/agent and independently drafts petitions for PTA reconsideration.
  • Participates in best practice group meetings in order to provide input and feedback to promote consistent administrative procedures.
  • Liaises with docketing group by providing guidance on USPTO prosecution as it pertains to deadlines and workflows that impact the paralegal group.
  • Advanced oral, writing, and communication skills including procedural document writing skills.
  • Excellent organizational and accountability skills, takes initiative to follow up with inventors, counsel and agents to meet critical deadline dates.
  • Sets own standards of high performance and works to exceed standards; takes initiative to expand own knowledge of PTO rules.
  • Assists with onboarding and mentoring legal assistants and paralegals and provides backup support when needed. Frequently provides backup and support to legal assistants and paralegals. Demonstrated track record and valued resource to management.

General
  • Expert knowledge of Microsoft Office 2013 including Outlook, Word, Excel
  • Advanced knowledge of IP Management Software and Document Management Software
  • Advanced form editing capability in Adobe Acrobat Pro
  • Advanced proficiency in use of basic to advanced forms including IP Management Software generated forms.
  • Strong skills and experience with Patent-In software to generate sequence listings.
  • Proficient knowledge and use of domestic and foreign patent databases, e.g., PCT Scope; EPO Online, etc.
  • Advanced reference management proficiency including searching, procurement of patent references (U.S. and Foreign patents, journal articles) and familiarity with reference linking within IP management software or document management system.
  • Advanced docketing experience working in an IP Management software application and the ability to provide docketing project support.
  • Advanced edit capability in Chemdraw.
  • Ability to quickly learn and adapt to new software, processes, and workflows in order to perform efficiently and provide key feedback to assist team members to maximize efficiency.
  • Timely and efficient communicator with patent attorneys/agents, outside counsel firms, team members, cross-functional groups and stakeholders

Administrative
  • Process and reconcile expense reports.
  • Experienced and organized travel arranger
  • Organizes small and large group meetings for attorneys/agents including meeting agenda and meeting minutes preparation.
  • Consistently seeks out opportunities to provide support when there are gaps in coverage.

Qualifications:
  • Bachelor's Degree or equivalent experience which is defined as 4 years of legal work experience above the minimum work experience required for the role. 10+ years of work experience or Paralegal Certificate and 8+ years of work experience in a law firm, an in-house legal department, a consulting firm, or comparable experience elsewhere.

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science™ ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Refer code: 7131782. Bristol-Myers Squibb Company - The previous day - 2023-12-16 18:26

Bristol-Myers Squibb Company

Cambridge, MA
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