Principal Clinical Scientist, Enfortumab vedotin

Principal Clinical Scientist, Enfortumab vedotin

01 Nov 2021
Washington, Bothell, 98011 Bothell USA

Principal Clinical Scientist, Enfortumab vedotin

Principal Clinical Scientist, Enfortumab vedotinClinical AffairsBothell,

WashingtonApplyDescriptionSummary: The Principal Clinical Scientist, Clinical Development will be responsible for supporting clinical trials and the development strategy for the Enfortumab vedotin program. The successful candidate will report to the Sr. Medical Director and should have demonstrated proficiency in clinical trials and supporting development programs, in addition to being adept at managing relationships across collaborations and with the external clinical community.Principal Responsibilities: Participate in the development of clinical protocols and amendments, investigator brochures, and clinical study reports

Contribute to the strategic development of both early and late stage clinical programs

Provide appropriate medical monitoring for ongoing clinical studies

Evaluation of safety, pharmacology, and efficacy data from ongoing and completed studies

Prepare manuscripts, abstracts and presentations for scientific meetings

Prepare content of Advisory Boards

Participate in regulatory submissions to US and foreign agencies

Conduct literature reviews and prepare summaries to support clinical development programs

Medical resource for design and interpretation of clinical and preclinical programs to support existing and new development candidates

Mentor junior Clinical Scientists

Qualifications:Demonstrates a passion for helping patients with cancer and for the science of oncology

Has a strong leadership presence with an ability to work effectively with other clinical and scientific leaders

Has a collaborative style with internal company leadership, external development partners and investigators/medical professionals

Is a team player, works well in a team environment both as a leader and a key contributor

Has a global perspective and mindset, with the ability to work effectively with colleagues from myriad cultures, backgrounds, and geographies

4+ years of industry experience in oncology drug development


MD, MD/PhD, PhD (biosciences or statistics), PharmD, APRN or PA

As the leading employer in our industry in the Pacific Northwest, Seattle Genetics is proud to offer a competitive total compensation package as well as a comprehensive benefits program designed to support the whole lives of our employees and their families. Benefits include medical, vision and dental coverage, group and supplemental life insurance, 401(k) with company match, tuition reimbursement, relocation assistance and much more. To learn more about Seattle Genetics, please visit Genetics is an equal opportunity employer. All qualified applications will receive consideration for employment without regard to race, age, gender identity, sexual orientation, color, religion, sex, marital status, national origin, protected veteran status, disability status, or any other status protected by federal, state, or local law.#LI-TC1

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