Arvinas is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases through the discovery, development, and commercialization of therapies that degrade disease-causing proteins. Arvinas uses its proprietary PROTAC Discovery Engine platform to engineer proteolysis targeting chimeras, or PROTAC targeted protein degraders, that are designed to harness the body’s own natural protein disposal system to selectively and efficiently degrade and remove disease-causing proteins. In addition to its robust preclinical pipeline of PROTAC protein degraders against validated and “undruggable” targets, the company has three investigational clinical-stage programs: ARV-766 and bavdegalutamide for the treatment of men with metastatic castration-resistant prostate cancer; and vepdegestrant (ARV-471) for the treatment of patients with locally advanced or metastatic ER+/HER2- breast cancer. Arvinas, as part of its overall business strategy, selectively assesses opportunities for potential collaboration, license, marketing and royalty arrangements, and similar transactions, to advance and accelerate the development and enhance the commercial potential of its product candidates.

　　#TeamArvinas is made up of approximately 450 passionate and curious employees, whose diverse thoughts and perspectives are highly valued. Arvinas employees embrace the freedom to pursue innovation, think creatively, and give back. They are driven by the company’s values and mission – to improve the lives of patients with serious diseases by pioneering therapies created with our revolutionary PROTAC® protein degradation platform. We’re really excited about the work we’re doing inside and outside of Arvinas, and think you will be, too. But don’t just take our word for it –  learn more about life at Arvinas and what employees have to say .

　　For more information, please visit www.arvinas.com .

　　Position Summary

　　Arvinas has an outstanding opportunity for an experienced Medical Affairs professional. The selected candidate will be responsible for overseeing the implementation of the Medical Affairs research program (e.g., Investigator-Sponsored Research (ISR), Research Collaborations (RC), and Expanded Access Program (EAP)) and medical education grant (e.g., CME) program. The candidate will play a crucial role in driving operational excellence, fostering collaborations, and ensuring the success of these medical affairs programs.

　　This position reports to the Senior Director, Medical Affairs Operations, and can work remotely from any location within the U.S.

　　Principal Responsibilities

　　Medical Affairs Research Program

　　Lead the development and implementation of the Medical Affairs research program, which includes Investigator-Sponsored Research (ISR), Research Collaborations (RC), and Expanded Access Program (EAP)/Compassionate Use studies.

　　Provide operational oversight of the ISR/RC studies; including the intake and review process, contracting, study activation and closure.

　　Establish and manage effective mechanisms to track progress toward study milestones; ensure communication of timely insights, identification of improvements needed, and implementation of corrective actions as needed.

　　Oversee budget tracking and forecasting for the Medical Affairs research program.

　　Ensure all Medical Affairs research program records are up-to-date and readily accessible for team use and audit readiness.

　　Ensure compliance of all Medical Affairs research program activities with company policies and procedures, identifying and escalating any risks or issues.

　　Independent Medical Education (IME) Grant Program

　　Lead the development, implementation, and audit readiness of the Independent Medical Education (IME) grants program.

　　Provide operational oversight of IME programs, including grant submissions, review, contracting, and internal reporting.

　　Create and maintain tracking tools for IME grant status and activities, including reporting and analyses of program outcomes.

　　Oversee budget tracking and forecasting for the IME grant program.

　　Ensure compliance of all IME programs with company policies/procedures, and Accreditation Council for Continuing Medical Education (ACCME) guidelines as applicable.

　　Qualifications

　　8+ years of relevant experience in the Biotech or Pharmaceutical industry.

　　Experience leading and managing Investigator Sponsored Research/Collaborative Research Programs.

　　Strong understanding of Medical Education/Pharmaceutical Industry guidelines (OIG, ACCME, and PhRMA) and regulations.

　　Must be detailed oriented and experienced in establishing new processes within Medical Affairs.

　　Must be able to both lead and execute the program independently and collaboratively in a fast-paced, matrixed, team environment.

　　Superior communication and interpersonal skills; effective interaction with cross functional team members.

　　Demonstrated planning, organization and time management skills including the ability to support and prioritize multiple projects.

　　Excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.

　　Strong understanding of clinical drug development and lifecycle management.

　　Education

　　Bachelor’s Degree, preferably in life sciences or healthcare field, is required.#LI-Remote

　　Arvinas is proud to offer a competitive package of base and incentive compensation as well as a comprehensive benefits program designed to support the health, wellness and financial security of our employees and their families. Benefits include group medical, vision and dental coverage, group and supplemental life insurance, and much more. To learn more about Arvinas, please visit www.arvinas.com

　　Arvinas is an Equal Opportunity Employer