Director - Global Regulatory Lead - Lexington, United States - Novo Nordisk

Novo Nordisk
Novo Nordisk
Verified Company
Lexington, United States

2 weeks ago

Mark Lane

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Mark Lane

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Description

About the Department


Our East Coast Global Development Hub brings together the best minds in life science innovation with facilities in Lexington, MA and Plainsboro, NJ.

We support programs from early research through late-stage clinical development.

We are building for the future, creating a distinct R&D community based on collaboration, partnerships, and cutting-edge research across multiple innovative modalities and therapeutic areas.

Our East Coast Global Development Hub merges biotech speed and agility with large pharmaceutical company quality, resources, and stability, uniting the best of both worlds to develop new medicines for patients.

We recognize that improving human health starts here and that patients rely on us. We're changing lives for a living. Are you ready to make a difference?


The Position
We are seeking a collaborative and science-driven global regulatory expert who wants to work with innovative investigational medicines.

You will lead a global regulatory team to develop and execute regulatory strategies for high impact projects while working with decision-makers across multiple functional areas.


Relationships
This role will work with the team both in the US and Denmark.


Essential Functions

  • Serve as a member of the Global Project Team (GPT) utilizing precedent and experience to develop innovative and flexible approaches to achieve development goals, advise on development strategies, and deliver on associated regulatory activities
  • Lead the Global Regulatory Matrixed Team in defining and executing the global regulatory strategy for assigned programs to ensure timely and highquality regulatory deliverables to the GPTs
  • Lead health authority interactions, including leading team through creation of briefing materials and meeting preparation
  • Lead and/or support global filing activities for submissions
  • Present regulatory strategies including communication of regulatory risks and associated mitigation plans to management and other internal stakeholders
  • Research and analyze the evolving competitive and regulatory landscapes to maintain current knowledge
  • Effectively manage timelines while working in a fastpaced and dynamic environment across both time zones and cultures

Physical Requirements
10-20% overnight travel required. Ability to lift 0-10 lbs.


Development of People


Ensure that reporting personnel have individual development plans (IDP), with annual goals and measurements that are consistent with the priorities of the business, and that interim reviews are held so that their work is focused on those priorities, and they understand their level of accountability for results and the measurement process.


Ensure that the IDP forms include completed learning and aspiration plans and are in place for all reporting personnel to enable the achievement of goals and capability to assume increased levels of responsibility.


Qualifications

  • A Bachelor's degree in a scientific discipline is required/an advanced degree is strongly preferred
  • Minimum of 10 years drug development/FDA/regulatory related industry experience required
  • Demonstrated knowledge of global regulatory requirements for drugs and biologics
  • Proven ability to develop robust regulatory strategies required
  • Experience interacting directly with regulatory authorities on an international scale
  • Experience preparing teams for and leading meetings with regulatory agencies, including the FDA
  • Experience with rare disease drug development, innovative trial design and/or expedited regulatory pathways, highly desired
  • Experience in setting direction for, leading, and motivating a team to work for joint objectives
  • Excellent verbal and written communication skills
  • Strong organizational and demonstrated problemsolving capabilities
  • Ability to thrive in a busy environment and maintain a positive attitude under pressure
The base compensation range for this position is $[ ] to $[ ]. Base compensation is determined based on a number of factors. This position is also eligible for a company bonus based on individual and company performance.

Novo Nordisk offers long-term incentive compensation and or company vehicles depending on the position's level or other company factors.


Employees are also eligible to participate in Company employee benefit programs including medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; employee assistance program; tuition reimbursement program; and voluntary benefits such as group legal, critical illness, identity theft protection, pet insurance and auto/home insurance.

The Company also offers time off pursuant to its sick time policy, flex-able vacation policy, and parental leave policy.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company
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