Senior Medical Director-Biotech Unit
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.
Reporting to the Clinical Development Lead, Biotech Unit (BU), the position is a member of BU and contributes to clinical development strategy and supports successful execution of clinical development programs in BU.
Leveraging deep therapeutic and functional area expertise, the incumbent will play a key role in medical monitoring for pivotal stage studies, will be accountable to jointly develop clinical program strategy and help assure that activities are executed within expected scope, budget and timelines. The incumbent will work closely with colleagues in clinical development, program leadership, biometrics, clinical operations, safety/pharmacovigilance, regulatory, molecular diagnostics, and translational research to ensure successful deliveries by study team.
Essential Functions of the Job:
- Facilitate generation of, author, update, and/or review key documents, including, but not limited to:
- Protocol concepts, synopses, protocols, and amendments of Informed consent documents;
- Investigator Brochures, Clinical study reports;
- Abstracts, posters and manuscripts o Clinical sections of INDs (and equivalent applications), NDAs (and equivalent applications), Annual Reports, and Developmental Safety Update Reports;
- Clinical sections of Health Authority Briefing Documents, Orphan Drug applications, and annual reports;
- Risks / benefits analysis for applicable documents;
- Clinical Development Plans.
- Partner with clinical operations and other functional areas for the successful implementation and execution of clinical studies.
- Provide scientific expertise for selection of investigator and vendors.
- Train BeOne colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or clinical protocol.
- Provide scientific and medical support throughout conduct of a clinical trial; respond to clinical questions from sites, IRBs/IECs, Health Authorities, and CRO’s.
- Review, query, and analyze clinical trial data.
- Interpret, and present clinical trial data both internally and externally.
- Represent a clinical study or development program on one or more teams or subteams.
- Create clinical study or program-related slide decks for internal and external use.
- Build and maintain opinion leader/investigator networks; organize and present at key opinion leader advisory boards and investigator meetings.
- Contribute to or perform therapeutic area/indication research and competitor analysis.
- Build strong relationships with internal experts.
- Identify continuous process improvement opportunities.
- Identify incremental organizational resource needs – staff, budget, and systems.
- Develop, track, execute and report on goals and objectives.
- Support budget planning and management.
- Be accountable for compliant business practices.
Basic requirement and experience :
- 6+ plus years of experience and success within other biotech/pharmaceutical companies.
- MD or DO or international equivalent degree required.
- Previous participation in a clinical development program is essential, including involvement in all stages of clinical trials (i.e. from start up to study report), ideally having taken at least one study through from start to finish in a clinical development role.
- Minimum 3 years relevant work experience in oncology clinical development. Experience in conducting lung Cancer clinical trials strongly preferred.
- Expert understanding of global clinical study design and drug development process from discovery to registration and post-marketing.
- High level of communication (written and verbal), interpersonal, organizational, and cross functional collaboration ski