Associate Director, Medical Writer - Publications

BeiGene

3d•$143,900 - $193,900•Remote

About The Position

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. We are seeking a highly experienced and strategically minded Medical Writer to lead the tactical execution of publications stemming from our global medical affairs publication plans. These plans span across early phase development to marketed products. In this role, the Medical Writer will serve as a key partner in shaping the external scientific narrative, as well as ensuring data are communicated with clarity, accuracy, and impact through high-quality publications and congress materials. This is an individual contributor, remote position.

Requirements

Advanced degree (PhD, PharmD, MD, or MS) in life sciences or related field; oncology specialization strongly preferred.
Minimum of 5-7 years of relevant medical writing experience, with a strong emphasis on global publication planning and congress communications, gained through working within the biotechnology/pharmaceutical sector or at a medical communications agency.
Excellent written and verbal communication skills, with a keen eye for scientific accuracy and editorial quality.
Experience working globally, cross functionally, and cross culturally.

Nice To Haves

Prior experience writing publications in clinical oncology (hematology or solid tumor) and/or health economic and outcomes research in the oncology space.
Familiarity with global regulatory and medical affairs environments (eg, US, EU, APAC).
Experience with publication agency oversight and publication steering committees.
Active membership in ISMPP, AMWA, EMWA, or related organizations.

Responsibilities

Develop strategic, high-impact scientific publications and congress materials in oncology.
Collaborate with cross-functional teams and external experts in a biotech or pharmaceutical setting.
Ensure adherence to GPP, ICMJE guidelines, and global compliance standards in medical publications.
Manage multiple concurrent projects and regions, prioritizing effectively.
Adhere to industry-standard guidelines as well as BeOne SOPs, work instructions, and quality standards.
Establish and maintain professional relationships with internal colleagues, external authors, journal editors, publishers, and other professional bodies.