Associate Director, Legal Italy at BristolMyers Squibb
Roma, Lazio, Italy -
Full Time


Start Date

Immediate

Expiry Date

14 Sep, 25

Salary

0.0

Posted On

15 Jun, 25

Experience

8 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Pharmaceutical Industry, English, Italian

Industry

Legal Services

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. 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 .
The Associate Director, Legal will provide legal support at BMS Srl , concerning regulatory, pharmaceutical and commercial law; managing litigation and evaluating the legal and technical aspects of all projects of the various functions regarding Decree D.lgs. 231/01, in line with company and Group policies and procedures and the current legislation

Key responsibilities and Major duties:

  • Contribute to the Legal Department advice at the company functions, regarding for example the correct application of procedures, Legislative Decree 231/01, privacy, taking care of the search for applicable legislation and jurisprudence.
  • Support the Business Units, providing legal advice on business management activities.
  • Support the Tender Office providing legal advice.
  • Support the Market Access function, in particular the Government & Regional Affairs depts., advising on regional legislation.
  • Support the Medical Direction projects, analyzing and understanding the internal customer and administration requirements and researching supporting legislation.
  • Support the Congress and Marketing depts. in preparing the documentation for events, conferences and products.
  • Participate in international project teams on specific products, taking care of the documentation and maintaining relationships with marketing, regulatory and medical on BMS products.
  • Support the company bodies responsible for supervision pursuant to Legislative Decree. 231/2001 and compliance, in line with current legislation and internal procedures.
  • Participate in special projects led by Farmindustria, coordinating working groups (e.g. in corporate law).
  • Keep up to date on all new legislation and jurisprudence on issues of interest to BMS Italy, in line with the corporate legal policies.

Requirements

  • Law degree
  • Previous experience (8 -10 years) as lawyer in multinational companies, preferably in the pharmaceutical industry.
  • Understanding of the pharmaceutical sector.
  • Solid and diversified knowledge in the legal field.
  • Fluency in Italian and in English.
Responsibilities
  • Contribute to the Legal Department advice at the company functions, regarding for example the correct application of procedures, Legislative Decree 231/01, privacy, taking care of the search for applicable legislation and jurisprudence.
  • Support the Business Units, providing legal advice on business management activities.
  • Support the Tender Office providing legal advice.
  • Support the Market Access function, in particular the Government & Regional Affairs depts., advising on regional legislation.
  • Support the Medical Direction projects, analyzing and understanding the internal customer and administration requirements and researching supporting legislation.
  • Support the Congress and Marketing depts. in preparing the documentation for events, conferences and products.
  • Participate in international project teams on specific products, taking care of the documentation and maintaining relationships with marketing, regulatory and medical on BMS products.
  • Support the company bodies responsible for supervision pursuant to Legislative Decree. 231/2001 and compliance, in line with current legislation and internal procedures.
  • Participate in special projects led by Farmindustria, coordinating working groups (e.g. in corporate law).
  • Keep up to date on all new legislation and jurisprudence on issues of interest to BMS Italy, in line with the corporate legal policies
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