Associate Director/Director, Global Regulatory Affairs Strategy

Permanent employee, Full-time · Boston (USA)

Be part of our team

As the Associate Director/Director, Global Regulatory Affairs Strategy, you will provide regulatory strategy support in partnership with cross functional teams and subject matter experts and manage regulatory aspects through all phases of development of our antibody-drug conjugates (ADCs) global clinical trials.

You will represent Regulatory Affairs on cross-functional teams, lead the planning and preparation of clinical trial submissions (INDs, CTAs, amendments, briefing documents, Investigator Brochures) and support global health authority interactions.

This position will report to the Senior Vice President, Regulatory Affairs within the Clinical Development department and be based in Boston, MA or possible remote opportunities within other locations within the U.S.

Your mission

Support the development and execution of global regulatory strategies for products and programs within the global portfolio.
Serve as the Regulatory Affairs representative on global project teams and Study Execution Teams, providing regulatory input and ensuring alignment with program objectives and timelines.
Prepare and coordinate high-quality regulatory global submissions, including BLAs, INDs, CTAs, amendments, annual reports, DSURs, Investigator Brochures, and briefing documents.
Support planning and execution of regulatory interactions with health authorities (e.g., FDA, EMA, Health Canada, MHRA), including meeting requests, briefing packages, and follow-up correspondence.
Monitor the global regulatory landscape to identify requirements, trends, and potential impact on development programs.
Coordinate and maintain health authority reporting schedules in collaboration with cross-functional teams.
Partner with external vendors (e.g., CROs, regulatory consultants) to ensure high-quality and timely submissions.
Support development of Regulatory Affairs departmental policies, SOPs, and systems (e.g., Veeva) to enhance submission quality and efficiency.
Assist in risk assessment and mitigation planning for regulatory deliverables.

Your profile

Bachelor’s degree in a scientific discipline required; advanced degree (MS, PharmD, PhD) preferred.
Minimum of 5 years in Regulatory Affairs (Strategy).
Direct experience preparing and submitting clinical trial applications (INDs, CTAs) and managing regulatory authority correspondence.
Knowledge of global regulatory requirements for clinical development (FDA, EMA, ICH guidelines).
Oncology therapeutic area experience strongly preferred.
Late-stage development regulatory experience, preferably including working on a significant submission (eg NDA or BLA, MAA) is a plus.
Excellent organizational, communication, and problem-solving skills
Ability to manage multiple priorities and work effectively in a dynamic and collaborative environment,
Demonstrated ability to work both independently and collaborate within cross-functional, matrixed teams.

Why us?

At Tubulis, curiosity and innovation drive us to transform cancer treatment. We are a fast-growing biotech where science meets passion—and where you have the chance to grow with us.

Impact that matters: Contribute to breakthrough therapies.
Global mindset: Work in an international, diverse team.
Grow & thrive: Develop your career in a supportive, fast-moving environment.
Innovation every day: Push boundaries with cutting-edge science.

At Tubulis, your ideas matter, your growth matters—and together, we make a difference.

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About us

The development of novel, effective and safe therapies for the treatment of cancer is one of the main challenges for modern medicine. We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of targeted therapeutics and antibody-drug conjugates (ADCs). With a strong team, our own technologies and innovative therapeutic concepts, we are ushering in a new era in the ongoing fight against cancer and share the vision of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers.

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We’re excited to learn more about you!

We appreciate your interest in applying to Tubulis.

Please complete the short form below. If you experience any issues uploading your documents, feel free to contact us at career@tubulis.com.