外資系大手製薬メーカー Senior Manager, Field Medical Affairs

資格・要件

A PhD, PharmD, or MD preferred, though a Master’s Degree with extensive oncology experience may be considered.

At least 6 years of relevant experience in pharmaceutical industry or clinical settings, such as drug information or disease management programs.

Proven expertise in oncology, particularly lung cancer, solid tumors, or hematology oncology.

Immuno-oncology experience is preferred.

職務内容

we are expanding our Field Medical Affairs team to bring innovative solutions in oncology and hematology oncology to the forefront. As a Senior Manager, Field Medical Affairs, you will play a pivotal role in advancing scientific exchange, collaborating with therapeutic area experts, and supporting clinical development initiatives. Join us in shaping the future of healthcare while contributing to meaningful, impactful work in a dynamic and collaborative environment.

A Typical Day:
As part of your role, you will:

Identify and maintain relationships with medical and therapeutic area experts, investigators, and other stakeholders.

Respond to scientific and clinical inquiries in compliance with industry regulations.

Perform disease management and therapeutic area education for practitioners, payers, and researchers.

Attend medical conferences to gather and report scientific, clinical, and competitive intelligence.

Collaborate with investigators and internal medical affairs teams to support investigator-initiated studies (IIS).

Assist in the development and communication of clinical data through abstracts, posters, presentations, and manuscripts.

Support site initiation and enrollment activities for clinical trials.

Ensure adherence to company policies, procedures, and compliance standards.

This Role May Be For You If:

You are passionate about oncology and have deep knowledge in lung cancer, solid tumors, or hematology oncology.

You thrive in a collaborative, matrix organization and enjoy building relationships in academic and clinical practice settings.

You have excellent communication skills and are fluent in both Japanese and English.

You are experienced in immuno-oncology and clinical trials, and possess a strong commitment to compliance.

You are comfortable traveling 30–50% of the time to engage with stakeholders and attend conferences.