Medical Director, Oncology US (remote) at Millipore Corporation in BILLERICA, Massachusetts

Posted in Other 1 day ago.





Job Description:

Work Location: Billerica, Massachusetts
Shift: No
Department: HC-RD-ODT Oncogenic Signaling
Recruiter: Rena Ann Peterson



This information is for internals only. Please do not share outside of the organization.




Your Role



As a Medical Director in Global Clinical Development Oncology, you will lead the development and execution of clinical strategies for oncology projects. You will provide strategic and medical leadership across cross-functional teams, guiding clinical studies from early to late-stage development and collaborating with the Global Project Team (GPT).


Key Accountabilities:


• Oversee clinical study projects from Phase 1 to Phase 3 within the Clinical Team.


• Serve as a clinical expert in dedicated programs within the GPT.


• Design clinical development strategies for early and late phases.


• Potentially supervise Clinical Research Scientists (CRS).


• Offer medical expertise for business development, discovery, stratified medicine, and regulatory affairs.


• Develop clinical plans, study concept sheets, and protocols in collaboration with team members.


• Ensure high-quality clinical documents, including protocols, reports, and Investigator Brochures.


• Review and approve clinical documents and analyze study data.


• Provide medical supervision for assigned projects/programs.



Who You Are




Minimum Requirements:



• MD with expertise in clinical drug development.


• Minimum 3 years of experience in clinical R&D within the pharmaceutical or biotech industry.


• Experience interacting with Health Authorities in Europe, the US, and possibly Japan/China.


• Ability to work in a matrix environment and within international cross-functional teams.


• Strong team player with excellent communication skills in English.



Preferred Requirements:



• Experience in oncogenic signaling clinical development.


• Familiarity with R&D interface partners (e.g., Regulatory Affairs, Clinical Pharmacology).


• Project management skills.


• Understanding of R&D and non-R&D partner needs.


• Strong analytical skills, strategic orientation, and initiative.


• Ability to multitask and adapt in a dynamic environment.


Pay Range for this position: $230,000 to $309,000


Our ranges are derived from several sources, and largely reliant on relevant industry market data. Should we decide to make an offer, we will consider several factors, including but not limited to your location, skills, experience, career level, and other job-related factors. This role may offer the following benefits: medical, vision, and dental insurance; life insurance; disability insurance; a 401(k) matching program; paid time off; and paid holidays; among other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including, but not limited to, cash bonuses.


The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.


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