Talent.com
Senior Director, Regulatory Strategy Consulting
Senior Director, Regulatory Strategy ConsultingHalloran Consulting Group, Inc. • Boston, MA, United States
Senior Director, Regulatory Strategy Consulting

Senior Director, Regulatory Strategy Consulting

Halloran Consulting Group, Inc. • Boston, MA, United States
[job_card.variable_days_ago]
[job_preview.job_type]
  • [job_card.full_time]
[job_card.job_description]

Senior Director, Regulatory Strategy Consulting

Are you looking for a company that is committed to improving human health, and a role that will develop and challenge you to think innovatively? Join Halloran’s Regulatory team as a Senior Director, Regulatory Strategy Consulting today!

Reporting to the Vice President of Regulatory Affairs, this leader will shape and drive global regulatory strategies across diverse therapeutic portfolios.

In this role, you will combine deep regulatory expertise, strategic foresight, and business development acumen to deliver innovative solutions for our clients. You will lead cross‑functional teams, represent clients in critical health authority engagements, and act as a trusted partner to senior leadership.

The ideal candidate thrives at the intersection of strategy and execution, balancing technical mastery with consultative leadership to deliver meaningful impact for clients and the organization.

Regulatory Strategic Leadership

  • Provide regulatory strategy and leadership to our clients through design and implementation of global regulatory strategies across development programs, proactively identify and mitigate regulatory risks to ensure alignment with client business objectives.
  • Lead the planning of major global regulatory submissions (INDs, CTAs, NDAs, BLAs) and responses, represent the client in meetings with FDA and global health authorities, lead rehearsals, and moderate live health authority meetings and partner with internal teams and external client teams / vendors to ensure quality, timely, and compliant regulatory submissions and deliverables.
  • Drive delivery team accountability for regulatory milestones and timelines; elevate and resolve critical path issues.
  • Meet a target billable utilization of 50% while driving client satisfaction and delivery excellence.

Team Leadership and Talent Development

  • Provide line management and performance management to inform optimal resource planning and oversee billable utilization tracking for direct reports.
  • Support team capacity planning and utilization trending to ensure optimal resourcing and project delivery across the portfolio of projects.
  • Coach and mentor and guide regulatory teams, to demonstrate the tools, skills, and resources needed to perform their job responsibilities. Foster a culture of innovation, collaboration, and continuous professional development.
  • Business Development and Account Growth

  • Partner with Business Development leadership to foster the continuation and of strong, long‑term relationships with clients and identify expansion opportunities for Halloran services. This includes participation in BD calls as the subject matter expert (SME), contributing and participating in generating a Response For Proposal (RFP), proposal development, BID defence meeting(s), as the SME.
  • Build and maintain strong relationships with clients to expand existing client relationships and identify new opportunities through consultative expertise and industry engagement. This will involve working closely with clients to understand their needs, leveraging the collective team to develop product‑specific strategies and solutions that meet client needs.
  • Ensure that clients are satisfied with the quality of our delivery product.
  • Understanding of industry trends and dynamics and the competitive marketplace to support business growth initiatives.
  • Identify new business and expand active accounts through networking, industry events, maintenance of client relationships and professional associations.
  • Operational Excellence and Process Improvement

  • Drive efficiencies across regulatory consulting processes, embedding best practices and governance mechanisms for consistent, high‑quality execution.
  • Thought Leadership and Industry Impact

  • Contribute to thought leadership rainmaking activities to influence and provide perspectives to our industry and clients.
  • Generate content (whitepapers, case studies) to showcase expertise and shape industry perspectives.
  • Provide presence at industry events, conferences and forums.
  • Support the development of marketing materials and social media posts that showcase Halloran’s expertise and breadth of expertise.
  • Other related duties and projects as required and assigned.
  • Qualifications

    Required :

  • Bachelor’s degree in scientific discipline with at least 15 years of Regulatory Affairs experience in the biotechnology and / or pharmaceutical industry.
  • Prior consulting or service provider experience and a demonstrated ability in managing high‑profile accounts and fostering client satisfaction.
  • Strong leadership skills in line management, coaching, and team development.
  • Proven track record leading cross‑functional, multi‑disciplinary teams and managing complex, high‑profile regulatory submissions.
  • Strong business development skills with experience in winning new business, expanding accounts, and serving as SME in client engagements.
  • Demonstrated strength in risk management, compliance governance, and process optimization.
  • Preferred :

  • Advanced degree (PhD, PharmD, MD, or MSc) and / or RAC certification.
  • Expertise within regulatory strategy, product development, and / or regulatory CMC.
  • Experience across multiple product types (e.g., biologics (proteins, mABs, ADCs), small molecules, cell and gene therapy, oligonucleotides, peptides).
  • Experience in central nervous system (neurology / psychology), metabolic, oncology, or rare diseases.
  • Compensation

    The targeted base compensation range for this position is between $200,000.00 and $260,000.00 annually. Please note : this compensation range is Halloran’s good‑faith and reasonable estimate of the range of possible compensation for this particular position at the time of posting; however, Halloran may ultimately pay more or less than the posted range.

    Halloran Benefits and Perks

    The benefits of being a Halloran employee go beyond the unparalleled opportunities of your day‑to‑day work! We offer an annual, discretionary bonus based on company and individual performance, comprehensive Medical, Dental, and Vision Insurance, and a 401(k) Plan for all full‑time employees. In addition to this, Halloran offers a flexible PTO Policy and opportunities for continued learning.

    Notice

    Halloran does not sponsor visas for employees.

    All remote employees are expected to have a consistent home internet connection with speeds of at least 25Mbps while working remotely.

    Halloran Consulting Group, Inc. is an equal‑opportunity employer committed to diversity, equity and inclusion in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, genetic information, veteran status, or any other characteristic protected by applicable federal, state, or local nondiscrimination laws.

    We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

    In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

    #J-18808-Ljbffr

    [job_alerts.create_a_job]

    Director Regulatory • Boston, MA, United States

    [internal_linking.similar_jobs]
    Associate Director Regulatory Affairs

    Associate Director Regulatory Affairs

    EPM Scientific • Boston, MA, US
    [job_card.full_time]
    Associate Director of Regulatory Strategy.A rapidly growing pharmaceutical company is expanding its regulatory leadership team and seeking a strategic, execution-oriented.Associate Director of Regu...[show_more]
    [last_updated.last_updated_variable_days] • [promoted]
    Associate Director or Director, Regulatory Affairs

    Associate Director or Director, Regulatory Affairs

    Kymera Therapeutics • Boston, MA, United States
    [job_card.full_time]
    Associate Director or Director, Regulatory Affairs.TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives.Kymera is deploying...[show_more]
    [last_updated.last_updated_variable_hours] • [promoted] • [new]
    Senior Director, Regulatory Strategy Consulting

    Senior Director, Regulatory Strategy Consulting

    Halloran Consulting Group • Boston, MA, United States
    [job_card.full_time]
    Career Opportunities with Halloran Consulting Group.Senior Director, Regulatory Strategy Consulting.Are you looking for a company that is committed to improving human health, and a role that will d...[show_more]
    [last_updated.last_updated_30] • [promoted]
    Senior Manager, Regulatory Affairs (Biosimilars)

    Senior Manager, Regulatory Affairs (Biosimilars)

    Fresenius Kabi USA, LLC • North Andover, MA, United States
    [job_card.full_time]
    The Senior Manager, Regulatory Affairs delivers Regulatory Affairs and compliance guidance and strategic input as a subject matter expert in Biosimilar Development and Life Cycle Management to find...[show_more]
    [last_updated.last_updated_30] • [promoted]
    Director, Regulatory Affairs - Clinical Strategy

    Director, Regulatory Affairs - Clinical Strategy

    Azurity Pharmaceuticals - US • Woburn, MA, US
    [job_card.full_time]
    Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing uniq...[show_more]
    [last_updated.last_updated_30] • [promoted]
    Senior Director, Global Regulatory Lead – Oncology (Hybrid)

    Senior Director, Global Regulatory Lead – Oncology (Hybrid)

    Takeda • Boston, MA, United States
    [job_card.full_time]
    A leading global biopharmaceutical company is seeking a Senior Director, Global Regulatory Lead – Oncology in Boston, MA. This role involves leading global regulatory strategy for complex oncology p...[show_more]
    [last_updated.last_updated_variable_days] • [promoted]
    Senior Regulatory Affairs Director - Oncology

    Senior Regulatory Affairs Director - Oncology

    AstraZeneca • Boston, MA, United States
    [job_card.full_time]
    Are you a strategically focussed Regulatory professional and would like to play an integral part in bringing life changing Oncology medicines to patients? If you are please read on!.At AstraZeneca,...[show_more]
    [last_updated.last_updated_30] • [promoted]
    Global Regulatory Strategy Director — Rare Diseases

    Global Regulatory Strategy Director — Rare Diseases

    OSI • Boston, MA, United States
    [job_card.full_time]
    A leading biotechnology company in Boston seeks a Sr.Director, Regulatory Strategist to lead global regulatory strategies and manage important regulatory submissions. Ideal candidates will have at l...[show_more]
    [last_updated.last_updated_variable_days] • [promoted]
    Senior Director, Regulatory Affairs

    Senior Director, Regulatory Affairs

    Formation Bio • Boston, MA, United States
    [job_card.full_time]
    Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development.Advancements in AI and drug discovery are creating more candidate drugs than the ind...[show_more]
    [last_updated.last_updated_30] • [promoted]
    Associate Director, Regulatory Affairs

    Associate Director, Regulatory Affairs

    eGenesis • Cambridge, MA, US
    [job_card.full_time]
    Genesis is dedicated to giving patients with organ failure a second chance at life by harnessing the power of genome engineering to create safe, effective, and readily available solutions.Reporting...[show_more]
    [last_updated.last_updated_variable_days] • [promoted]
    Director, Nonclinical Toxicology & Regulatory Strategy

    Director, Nonclinical Toxicology & Regulatory Strategy

    Stryker Corporation • Boston, MA, United States
    [job_card.full_time]
    A leading biopharmaceutical company seeks a Senior Toxicologist to manage nonclinical safety strategies for their development programs. The ideal candidate will have a Ph.Toxicology, 12-15 years of ...[show_more]
    [last_updated.last_updated_variable_days] • [promoted]
    Director, Regulatory Affairs Strategy

    Director, Regulatory Affairs Strategy

    BlueRock Therapeutics • Cambridge, MA, United States
    [job_card.full_time]
    BlueRock Therapeutics LP is a clinical stage cell therapy harnessing the power of cell therapy to create a pipeline of new medicines for people suffering from neurological and ophthalmic diseases.T...[show_more]
    [last_updated.last_updated_variable_days] • [promoted]
    Director, Regulatory Strategy

    Director, Regulatory Strategy

    Solid Biosciences • Charlestown, MA, US
    [job_card.full_time]
    Director, Regulatory Strategy – Solid Biosciences.Solid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromus...[show_more]
    [last_updated.last_updated_30] • [promoted]
    Senior Director, Global Regulatory Strategy Lead - Regulatory Affairs

    Senior Director, Global Regulatory Strategy Lead - Regulatory Affairs

    Olema Oncology • Boston, MA, United States
    [job_card.full_time]
    Senior Director, Global Regulatory Strategy Lead - Regulatory Affairs at Olema Oncology.Reports to the Senior Vice President of Regulatory Affairs. Location : Boston, MA or San Francisco, CA.Domestic...[show_more]
    [last_updated.last_updated_30] • [promoted]
    Hybrid Senior Director, Global Regulatory Strategy & Early Development

    Hybrid Senior Director, Global Regulatory Strategy & Early Development

    Alexion • Boston, MA, United States
    [job_card.full_time]
    A leading biopharmaceutical company in Boston is seeking a Senior Director, Global Regulatory Strategy.This role focuses on regulatory strategy for early-stage programs and requires extensive exper...[show_more]
    [last_updated.last_updated_variable_days] • [promoted]
    Senior Director, Regulatory CMC

    Senior Director, Regulatory CMC

    PepGen • Boston, MA, US
    [job_card.full_time]
    PepGen is at an exciting time in our development.This role is for a motivated and team-orientated individual who flourishes in an environment where they can help lead and shape our future.As an int...[show_more]
    [last_updated.last_updated_30] • [promoted]
    Senior Director / Vice President, Regulatory Affairs

    Senior Director / Vice President, Regulatory Affairs

    Korro Bio • Cambridge, MA, US
    [job_card.full_time]
    Korro is a biopharmaceutical company focused on developing a new class of genetic medicines for both rare and highly prevalent diseases using its proprietary RNA editing platform.Korro is generatin...[show_more]
    [last_updated.last_updated_variable_days] • [promoted]
    Global Director, CMC Regulatory Strategy (Biologics)

    Global Director, CMC Regulatory Strategy (Biologics)

    Blonde Inc. • Boston, MA, United States
    [job_card.full_time]
    A leading biotech company in Boston is seeking a Director of Regulatory Affairs, CMC to lead the global regulatory strategy across a portfolio of rare disease therapies. The role involves managing C...[show_more]
    [last_updated.last_updated_variable_days] • [promoted]