Medical Affairs Director
1 week ago
Join Net2Source Inc. as a Medical Affairs Manager and play a key role in the development and execution of global strategies for products in the LIFE franchise.
Job Summary:This is a global role that involves collaborating with internal and external stakeholders to develop and execute global strategic activities. The ideal candidate will have deep subject matter expertise regarding LIFE products and be able to lead the development of global strategic activities as well as develop and execute them on a tactical level.
Key Responsibilities:- Collaborate with internal and external stakeholders to develop and execute global strategic activities.
- Develop and execute global strategic plans for products in the LIFE franchise.
- Lead the development of global strategic activities and develop and execute them on a tactical level.
- Manage HBV Phase IV portfolio including liaising with key cross-functional partners such as clinical operations and local affiliates.
- Review abstracts and/or manuscripts that result from the phase IV program.
- Support the management and documentation of phase IV study status.
- Serve as Medical Affairs therapeutic area expert on Global Publications and Scientific Message Platform committees and other support for Scientific Communications.
- Provide medical and scientific coverage and support at key scientific meetings.
- Support project leads in the execution and tracking of their projects.
- Oversee medical and scientific review of promotional materials for GRC and MRC.
- Excellent written, verbal, and interpersonal, relationship-building and negotiating communication skills.
- Excellent organizational skills to support project planning across multiple activities, anticipate and prioritize workload.
- Excellent teamwork skills. Organized; attention to detail and able to meet timelines in a fast-paced environment.
- Excellent analytical and problem-solving skills, demonstrated ability to identify and understand complex issues and problems and identify and query key findings from study data and publications.
- Experience in public health or Internal Medicine (general or subspecialty) is highly desirable, in addition to clinical patient care.
- Experience in developing effective abstracts, manuscripts, posters, and slides and presenting at scientific meetings.
- Must be fully cognizant and adhere to regulatory and legal (Business Conduct) requirements for clinical trials and other Medical Affairs activities; thorough knowledge of FDA regulations, ICH guidelines and GCPs governing the conduct of clinical trials.
- Must be able to work with autonomy and independence.
- Ability to work around international time zones and ability to travel to and participate in domestic and international conferences which will include occasional weekend travel is required.
- Ability to work in a global environment which will require participation in meetings outside of standard work hours and on the weekends to accommodate time zone differences.
- Bachelor's degree a minimum, but M.D., D.O., PhD (biological or pharmaceutical sciences), or PharmD preferred. Prior experience in hepatology, infectious diseases, virology, or clinical virology a plus.
- Preferred experience in Medical Affairs and/or Clinical Research including Phase IIIb and IV studies; clinical trials management, medical monitoring, and scientific expertise.
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