Senior Medical Director, Clinical Development

Senior Medical Director, Clinical Development

Summary

The Senior Medical Director is a medical oncologist or a radiation oncologist who has clinical expertise in the oncology therapeutic area. This individual will be responsible for the clinical leadership of Phase 1-3 company sponsored studies and collaborate with imaging experts to provide clinical leadership for any phase 0 studies. Reporting to the CMO, this individual will partner with clinical operations, regulatory, medical writing, clinical pharmacology, stats / data management / programming, project management, and safety to provide clinical direction for company-sponsored clinical studies. In addition to clinical leadership for the company-sponsored studies, this individual will also be working with a clinical project scientist to review and provide input to investigator-initiated study proposals. When needed, this individual will also partner with the discovery team and the business development team to provide strategic input, to assess potential partnership and licensing opportunities.

Main Duties and Responsibilities

• Clinical Leadership :
• Primary responsibility for clinical and safety oversight of company sponsored Phase 0-3 clinical trials.
• Key clinical expert for study protocols and clinical development plans for each molecule in clinical development
• Key clinical stakeholder to answer health authority and IRB / ethics committee questions for the molecules in clinical development
• Works with medical writing and regulatory, and clinical operations to author protocols, investigator brochures, annual reports, clinical study reports and DSURs.
• Leads and when necessary supports clinical study start-up, data base locks, and study closeouts.
• Primary medical reviewer for ongoing and active company-sponsored studies
• Collaborate with cross functional partners to execute on clinical goals and objectives, ensuring timely achievement of milestones.
• Strategic Leadership :
• Lead clinical study teams, ensuring effective communication and coordination in partnership with the clinical operations team.
• Provide strategic input to potential partnership and licensing opportunities.
• Maintain the highest standards of clinical study and operational integrity.

Qualifications & Experience Required

About Us

ARTBIO is re-defining cancer care by developing a new class of radioligand therapies (RLT) which harness the power of 212Pb and deliver it directly to the tumour. Targeted RLT is one of the fastest growing areas of oncology research and investment. The foundational technology, termed AlphaDirect, was born out of elegant research by our scientific founders, Roy Larsen and yvind Bruland, inventors of XofigoTM. ARTBIO is leveraging this groundbreaking science and expediting novel drug discovery targets which broadly exploit the unmet medical need and opportunity in revolutionising cancer care. Supported by a committed group of investors, ARTBIO has built a highly experienced, multi-disciplinary team of drug-hunters and developers. For more information on our strategy and emerging pipeline, please visit www.artbio.com and follow-us on .

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

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.

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