Associate Director, Feasibility, Site Engagement and Strategic Planning & Operat

About us

BeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 10,000 colleagues spans five continents, with administrative offices in Basel, Beijing,and Cambridge, U.S. To learn more about BeOne, please visit www.beonemedicines.com and follow us on LinkedIn and X (formerly known as Twitter).

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.
Job Description:
General Description:

The Associate Director, Feasibility, Site Engagement, and Strategic Planning & Operations will play a pivotal role in shaping the strategic direction of clinical development in Malaysia & Singapore . This multifaceted position combines scientific rationale with operational expertise, driving site engagement and enhancing patient enrollment. You will collaborate with cross-functional teams and establish strong relationships with key opinion leaders (KOLs) and sites, ensuring our clinical trials are optimally positioned for success.
Essential Functions of the job:
Feasibility Assessment:

- Collaborate with regional counterparts across JAPAC to ensure consistent feasibility methodologies and alignment with global processes.

- Integrate local disease landscaping, epidemiological insights, and competitive intelligence into feasibility recommendations.

- Drive early feasibility planning in partnership with other functions such as clinical development, Regulatory Affairs etc. to shape protocol feasibility and strategical trial placement discussion.

Site Engagement:

- Build and maintain effective relationships with KOLs and key sites to foster collaboration.

- Leverage relationships for improved feasibility, site selection, and patient enrollment efforts.

- Collaborate with clinical teams to optimize site engagement strategies, mitigating recruitment challenges.

- Closely work with GCO senior leadership, rCSM, and cross-functional stakeholders

Strategic Leadership:

- Lead the development and implementation of integrated clinical strategies, working closely with local partner functions (e.g., Global Regulatory Solutions, Medical Affairs, Marketing) and the Global team.

- Analyze competitive market dynamics and propose actionable strategies to enhance operational performance.

Cross-Functional Collaboration:

- Serve as a key liaison between Clinical Development, Clinical Operations, Regulatory Affairs, and Medical Affairs to ensure cohesive strategy alignment.

- Facilitate effective communication and collaboration among diverse teams, driving the clinical development agenda forward.

Proactive Problem Solving:

- Anticipate challenges related to patient recruitment, proposing innovative solutions to sustain clinical momentum.

- Monitor and assess project progress, providing insights and recommendations to senior leadership.

Supervisory Responsibilities:

- Drive high level of ownership and accountability within team and with external stakeholders

- Provide mentoring and training to junior members in the team

Qualification Required:
Education Required:

Bachelor’s degree or higher in a scientific or healthcare discipline, and advanced degrees preferred. Minimum of 10 years of experience in clinical development within the pharmaceutical or biotechnology industry
Competencies:

- Scientific knowledge and operational acumen

- Cross-functional collaboration and communication

- Relation