Senior Medical Director

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Job 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

As Senior Medical Director for the novel modalities team, you will be part of building, leading and managing a team highly skilled medical doctors and guiding them in their daily work as well as securing their personal and professional development. You will manage relationships with internal and external key collaborators, including Novo Nordisk affiliates. Additionally, ensure the medical deliveries for key development and life cycle management projects within our siRNA portfolio.

You will report to the Vice President of Medical and Science and become a member of the area's management team and collaborate closely with the other managers in the area. You will take an active part in developing the area as well as a lead role in various improvement projects, including process optimization.

Relationships

Reports to: VP, Medical & Science.

Work with the VP Medical/Scientific Development, Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams.

Will be interfacing with both internal and external stakeholders including KOLs and Principal Investigators.

Essential Functions

Support the VP Medical/Scientific Development as the US/international clinical lead for DCR-PHXC program to both internally and externally facing stakeholders

Responsible for setting direction, leading, motivating, and developing team members

In conjunction with other relevant functional areas, help develop/ refine the strategic development plan for DCR-PHXC and other emerging novel therapeutics

Provide clinical and scientific expertise to the design of studies, writing of protocols and other study and regulatory-related documents for DCR-PHXC, and other programs

Participate in the analysis and interpretation of data, ensure integrity of trial data, and assist in reporting of study results including preparation of scientific summaries, abstracts and manuscripts

Provide leadership in the execution of clinical trials

Ensure compliance with SOPs, ICH, GCP and other national and international regulatory requirements

Work with the VP Medical/Scientific Development, Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams to deliver and drive the timely completion of all clinical activities related to DCR-PHXC and other emerging clinical-stage programs

Serve as a leading member, or participant, at multiple internal review groups and utilize novel and creative methods to resolve clinical development problems

Work with the larger Global Project Team to deliver excellent medical support for DCR-PHXC and other clinical-stage programs

Interface with US/international regulatory authorities, as appropriate, in support of the development objectives for DCR-PHXC and assist Regulatory Strategy staff in the compilation of submissions and in the responses to inquiries

Lend clinical expertise to the Statistical Analysis Plan development and data management, and work closely with statistical programming and data management on the project level

Act as a liaison between the company and clinical site investigators and KOLs

Interface together with VP Medical/Scientific Development with Safety Review Committees and Data Safety Monitoring Committees

Participate in safety review meetings and providing medical monitoring of ongoing clinical trials

Physical Requirements

10-20% overnight travel required.

Development of People

Supervisory

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.

Manage the application and communication of all Novo Nordisk policies, procedures, and Novo Nordisk Way.

Qualifications

MD or the international equivalent is required

4+ years Pharmaceutical/Biotech industry experience, including time managing clinical trials, or academic clinical research background

Demonstrable experience for setting direction, leading, motivating, and developing team members

Strong scientific background with experience in reviewing & interpreting scientific and study data is required

Track record of scientific publications strongly preferred

Working knowledge of biostatistics, data management, clinical operations and scientific and technical processes desirable

Working knowledge of applicable US and EU regulatory requirements and of the drug development process

Experience in building and maintaining effective relationships with external KOL's, advisory boards and other key external therapeutic area influencers desirable

Team player who works collaboratively in a challenging team matrix environment

Ability to work independently to resolve challenges and conflicts

Excellent written and oral communication skills

Integrity, honesty and highest ethical standards and a sense of personal accountability

Quickly adapt and provide innovative solutions to challenges as they present themselves

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 in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we're life changing.

Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.

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