Cynet Systems Inc.
Medical Communications Manager
Cynet Systems Inc., Lawrence Township, New Jersey, us, 08648
Qualifications and Experience:
PharmD, MD, PhD or equivalent.
Minimum of 3-4 years of Pharmaceutical/Healthcare industry experience with a focus on medical communications.
Ability to manage various projects, solve problems, deliver on commitments, and work with multidisciplinary teams.
Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate and collaborate.
Experience leading cross-functional, cross-cultural project teams, and collaborating across matrix, multiple markets and global geographies.
Experience leading medical communications across all phases of drug development and commercialization.
Ability to analyze and interpret trial data.
Preferred:
Experience in solid tumor oncology.
In-depth knowledge of Good Publication Practices and guidance (GPP, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication.
Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements.
Working knowledge of Microsoft suite of applications, and familiar with publication management tool (Data Vision).
PharmD, MD, PhD or equivalent.
Minimum of 3-4 years of Pharmaceutical/Healthcare industry experience with a focus on medical communications.
Ability to manage various projects, solve problems, deliver on commitments, and work with multidisciplinary teams.
Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate and collaborate.
Experience leading cross-functional, cross-cultural project teams, and collaborating across matrix, multiple markets and global geographies.
Experience leading medical communications across all phases of drug development and commercialization.
Ability to analyze and interpret trial data.
Preferred:
Experience in solid tumor oncology.
In-depth knowledge of Good Publication Practices and guidance (GPP, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication.
Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements.
Working knowledge of Microsoft suite of applications, and familiar with publication management tool (Data Vision).