Medical Affairs Manager [515]

Job description

Provide guidance and oversight related to health authority (FDA, EMA, MHRA, etc.) regulations that impact the Medical Affairs organization. May assist in development or review of Medical Affairs SOPs and other procedural documents. Participates in developing and presenting training using standard modules and training on compliance related topics. Participates in the periodic assessment and review of Medical Affairs GxP role-based training plans to suggest improvements to existing curriculums. Assists in audit readiness for regulatory agency inspections Supports Medical Affairs with internal or external routine audit activities and document reviews. Ability to work hybrid if local to the site only - NO Full remote Exp in a pharma Medial Affairs lead role. Ability to work W2 only $45 ph Excellent written/oral communication skills. Solid organizational & planning skills. Excellent problem-solving skills Please attach a WORD resume to your submission All of your information will be kept confidential according to EEO guidelines. ON-SITE only on W2 This is a contract role and does not offer benfits 40-hour week MEDVACON Life Sciences works with many leading pharmaceutical companies to hire contractors for projects & assignments in cGMP Quality, Compliance, Validation and CSV work. We're supporting our client in Foster City CA to hire contractors for several roles. This is an outstanding opp to work with colleagues across different therapy areas and functional teams (Clinical Operations, Business Conduct, etc)