Associate Director, Regulatory Affairs Contract (Boston) Job at Nuvation Bio, Inc., Boston, MA

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  • Nuvation Bio, Inc.
  • Boston, MA

Job Description

Who we are Nuvation Bio is a biopharmaceutical company tackling some of the greatest unmet needs in oncology by developing differentiated and novel therapeutic candidates. Our vision is to significantly change the practice of oncology by developing medicines that provide truly meaningful improvements in quality of life and survival for people with cancer. What youll be doing As a key member of the Nuvation Regulatory Affairs team, you will collaborate with a crossfunctional team to advance clinical stage programs and further develop commercial stage assets. We are looking for an experienced handson Regulatory Affairs professional to contribute to the development strategy and lead in the planning, preparation, submission and maintenance of regulatory submissions for Nuvation products.

  • Regulatory representative for drug development project teams with responsibility for developing or contributing to regulatory strategies and requirements
  • Responsible for the management, planning, coordination, and preparation of documents that are submitted to U.S. and, if required international, regulatory authorities, in support of INDs, NDAs, DMFs, CTAs, amendments, safety reports, and annual updates
  • Responsible for interactions and direct contact with regulatory agencies
  • Contributes to pharmacovigilance activities as needed
  • Interprets and communicates regulatory expectations to internal and external stakeholders (including partners, CROs, CMOs, consultants, and contractors) in order to execute program objectives in compliance with applicable regulations

What Knowledge & Experience youll bring to us

  • Bachelor or Masters degree required
  • Minimum of 10 years equivalent experience in drug development/regulatory affairs in the biopharmaceutical industry
  • Experience with drug development and commercial product regulatory requirements
  • Familiar with eCTD, e-publishing systems, and direct experience in preparing regulatory submissions is required; strong authoring and content editing skills required
  • NDA experience is preferred and experience with marketing applications outside of the US (e.g. MAA, NDS) desirable
  • Deep knowledge of FDA regulations is required
  • Experience with supporting global clinical studies is desired
  • Selfstarter and influential team player
  • A demonstrated ability to collaborate, as well as to work independently, across a diverse range of areas, balancing competing priorities in a fastpaced environment with a high level of professionalism
  • Located in Boston area preferred

Communication & Interpersonal Skills:

  • Excellent communication and interpersonal skills;
  • Stellar leadership skills for internal and external activities;
  • Must be able to write clearly and summarize information effectively;
  • Must be able to present complex information to various audiences;
  • High level organization skills as primary manager of internal docket coupled with exquisite attention to detail.

Behavioral skills to be successful

  • ProblemSolver As an actionoriented selfstarter, youre eager to apply your expertise in diagnosing inefficiencies, determining root causes, and recommending solutions to complex challenges.
  • Personable You establish and nurture highly effective relationships with colleagues and key stakeholders that support and advance project goals and objectives.
  • Credible Thorough understanding of clinical methodologies and providing sound analytical support, you quickly establish credibility as a reliable resource.
  • Emotional intelligence, curiosity, and a knack to figure out a way to build something better
  • Communication Effectively listens, conveys, and receives ideas. Maintains a consistent flow of information. A strong presenter and effective communicator with the ability to influence stakeholders.
  • Accountability Acts with a clear sense of ownership whether the task is in their role description. Holds yourself and others accountable to execute all tasks at hand through seen and unforeseen circumstances with high quality and integrity.
  • Adaptability Can manage in an environment of ambiguity. Embraces the change of a new system, process, technology, or idea in the organization. You could reassess priorities, alter goals and take risks.

What we have for you!

  • Competitive Base Salary, Bonus, and Equity Plans
  • Unlimited Vacation and 10 Sick Days Annually
  • Excellent Medical, Dental, and Vision Coverage
  • 401K with Company Matching
  • and much more!

Disclaimer Nuvation Bio, Inc. is an equal opportunity employer, and, in accordance with applicable federal, state, and/or local law, all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by the law.

The base pay offered will take into account internal equity and also may vary depending on the candidates job-related knowledge, skills, experience, and location among other factors. Our fulltime regular positions also include an annual performancebased bonus and longterm incentive units (equity) provided as part of our compensation package, in addition to a full range of medical, financial, and/or other benefits, depending on the level and position offered.

This job description reflects the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Nothing restricts managements right to assign or reassign duties and responsibilities to this job at any time.

Note to all external Recruiters & Staffing Agencies
All of our open positions are managed by our Talent Acquisition department. Any resumes submitted through the website or directly by recruiters or staffing agencies in advance of an executed agreement with Nuvation Bio, Inc., will be considered unsolicited and the company will not be responsible for any related fees. Resumes sent directly to employees or hiring managers will also not be accepted as referrals.

Nuvation Bio, Inc.

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Job Tags

Full time, Contract work, For contractors, Local area,

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