San Francisco Metro Area, CA
The Sr Manager of Medical Affairs POC will work closely with the Medical Affairs Lead and International Business team (IBT) to execute the medical plan along with key initiatives and strategies to support the global utilization of related Diagnostics products. As the Sr Manager for the disease specific area, she/he will contribute to the medical plan. As part of the plan, the Sr Manager will be responsible for activities related to executing non-registrational Clinical Trials. This includes managing the investigator initiated study program. The Sr. Manager will ensure that targeted data sets are presented at key scientific meetings and international congresses and to peer-reviewed journals according to the publication plan. The Sr. Manager will also communicate these activities and develop medical messages along with the business teams to support marketing plans. The Sr Manager will be responsible for supporting planning of scientific advisory boards and scientific symposia according to the medical plan. Other responsibilities include supporting the global commercial success of products.
Work with the cobas Liat Product Managers to support commercialization of Liat LCT/IBT products:
Conduct literature reviews and write publication summaries to keep business stakeholders up to date on recent evidence.
Work with communication lead to curate medical content and evidence to support business activities.
Work with opinion leaders to schedule speaking engagements and provide feedback on areas of interest
Contribute to the International Business Team (IBT):
Provides support of RMS scientific activities for product launches and post-marketing support through scientific material development, speaking events and publications
Work with regional Medical & Scientific Affairs representatives
Support execution of global scientific advisory boards including content management
Attendance at key (molecular) diagnostics scientific congresses to provide scientific support as well as congress feedback for the IBT
Execution of scientific symposia and educational events at key internal meetings and international scientific congresses, including managing speakers
Responsible for providing scientific and clinical support for affiliates
Review publications for scientific and medical content
Responsible for managing all non-registrational clinical trials:
Responsible for the implementation of global study support strategies and initiatives and facilitates open channels of communications across divisions to align these scientific strategies
Responsible for the execution, and reporting of non-registrational clinical trials
Contributes to managing the Scientific Affairs budget
Responsible for the RMD investigator initiated study program
Establishes and support the development of medical affairs processes which are aligned with the global medical activities across the division
Works with global key opinion leaders consistent with MSA strategies and initiatives.
Live Leadership Commitments and CoA Beliefs in day-to-day interactions
Training in virology and/or microbiology a plus
Experience with diagnostic implementation and/or point-of-care diagnostics ideal