Impress employers and recruiters.
Choose from hundreds of resume examples.

Target Resume Now

About the Role

Drive the development and publication of deliverables (e.g., conference presentations, papers) for assigned Evidence Generation activities, collaborating with internal and external stakeholders such as MAL/MIS/EOR/MSL. Understand how Medical Affairs contributes to business objectives and proactively execute Medical Affairs activities with MAL/MAD support, leveraging knowledge of Medical Affairs and disease/product areas. Manage assigned projects and provide partial support to MAL roles as needed.

Responsibilities

Drive the development and publication of deliverables for assigned Evidence Generation activities, collaborating with internal and external stakeholders.
Proactively execute Medical Affairs activities with MAL/MAD support, leveraging knowledge of Medical Affairs and disease/product areas.
Manage assigned projects.
Provide partial support to MAL roles as needed.

Requirements

3+ years of clinical/basic research experience in oncology or 3+ years of industry experience.
Knowledge level sufficient for professional discussions with KEEs (basic/clinical medicine, disease area, drug-related, statistics).
Knowledge of planning company-sponsored studies, reviewing concepts/protocols for investigator-initiated studies, and managing publications and progress of company-sponsored studies (knowledge of clinical research regulations, clinical study planning/execution, and manuscript writing).
Communication skills necessary to perform duties with stakeholders.
Knowledge of clinical research regulations and rules (e.g., laws, SOPs) enabling accurate operation based on clinical research experience.
Basic research or clinical experience in breast or gynecological cancer (preferred).
3+ years of industry experience in Medical or Development departments (preferred).
Team management experience (preferred).
Ability to travel.
Firm commitment to building a long-term career in the pharmaceutical industry.

Skills

Logical and strategic thinking.
Information gathering.
Project management and risk management knowledge and skills.
Ability to create high-quality documents and materials.
Leadership skills applicable in intra-functional, cross-functional, and cross-divisional teams and situations.
High communication skills (e.g., ability to reach rational agreements and conclusions, and elicit desired actions from others even in difficult situations with conflicting opinions).
Negotiation skills in English.
Reading comprehension of necessary papers and writing skills in English.

Location

Osaka
Tokyo

Work Type

Full-time

Experience Level

3+ years

Education Level

Bachelor's or Master's degree in a science field (Medicine, Pharmacy, Disease-related science).
MD or Pharmacist qualification (preferred).
MSc/MPH/PhD (preferred).

About the Company

AstraZeneca embraces diversity and equality of opportunity.
We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.
We believe that the more inclusive we are, the better our work will be.
We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.

Equal Opportunity

We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.