Senior Director, Regulatory Affairs in Cambridge

Senior Director, Regulatory Affairs in Cambridge

Cambridge Full-Time 136800 - 167200 $ / year (est.) On-site
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At a Glance

  • Tasks: Lead regulatory interactions and coordinate submissions for innovative cancer therapies.
  • Company: ARTBIO, a pioneering biotech redefining cancer care with cutting-edge radiopharmaceuticals.
  • Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
  • Other info: Join a passionate team dedicated to improving patient outcomes globally.
  • Why this job: Make a real difference in cancer treatment while working with groundbreaking technology.
  • Qualifications: Extensive experience in regulatory affairs and strong communication skills.

The predicted salary is between 136800 - 167200 $ per year.

Summary

The Senior Director, Regulatory Affairs leads and coordinates regulatory interactions and submission execution for ARTBIO's clinical-stage radiopharmaceutical programs.

This role is primarily responsible for coordinating regulatory medical writing across functions.

The position works cross-functionally to translate research and development data and strategy into clear, compliant regulatory communications and high-quality submission deliverables.

About Us

Channeling Energy. Changing Lives.

ARTBIO redefines cancer care by discovering and developing a new class of Alpha Radioligand Therapies (ARTs), powered by unique Pb-212 isotope technology and seamless supply.

Our team works tirelessly to bring therapies that matter to patients who need them.

The unique ARTBIO approach selects the optimal alpha-precursor isotope (212Pb) and tumor-specific targets to create therapeutics with the potential for the highest efficacy and safety.

The company's Alpha Direct TM technology, a first-of-its-kind 212Pb isolation method, enables a distributed manufacturing approach for the reliable production and delivery of ARTs.

ARTBIO is advancing multiple pipeline programs, with lead program AB001 currently in first-in-human trials.

The company is shaped by a long-standing scientific legacy with nearly a century of pioneering work in radiation therapy conducted at the University of Oslo and Norway's Radium Hospital.

Cancer is relentless. So are we.

We are driven by a desire to do better for cancer patients, lowering the burden of toleration and safety while at the same time raising the bar on clinical efficacy and duration.

As an emerging, global biotech with locations in Boston, Basel, London, and Oslo, we take advantage of diverse scientific depth and insights, which makes ARTBIO a unique place to work.

EEO Statement

ARTBIO is proud to be an equal opportunity workplace and is an affirmative action employer.

We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.

If you have a disability or special need that requires accommodation, please let us know.

ARTBIO does not accept unsolicited resumes from external agencies or recruiters.

Submission of a resume without a prior written agreement does not create any express or implied contract between ARTBIO and the agency.

ARTBIO will not pay any fees related to unsolicited resumes.

Senior Director, Regulatory Affairs in Cambridge employer: ARTBIO

ARTBIO is an exceptional employer, offering a dynamic work environment where innovation meets purpose in the fight against cancer. With a commitment to employee growth and development, team members are encouraged to collaborate closely with leading experts in the field, fostering a culture of continuous learning and impactful contributions. Located in vibrant cities like Boston, employees benefit from a rich scientific community and diverse perspectives, making ARTBIO a truly unique place to advance your career while making a difference in patients' lives.

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Contact Details:

ARTBIO Recruitment Team

We think you need these skills to ace Senior Director, Regulatory Affairs in Cambridge

Regulatory Affairs Expertise
Medical Writing
Cross-Functional Collaboration
Clinical Submission Execution
Compliance Knowledge
Data Translation Skills
Communication Skills