Associate Director, Regulatory Strategic Writing

Job reputed company: • Responsible for providing leadership and direction for clinical and regulatory writing reputed company for one large or multiple compounds reputed company a therapeutic area reputed company budget, with reputed company, and in accordance with timelines. • Directly leads multiple individual contributors located in geographically disbursed locations with reputed company of both reputed company staff. • Assists in the selection of freelance consultants or other vendors. • Participates in continual improvement across Strategic Medical Writing best practices, processes, and performance. • Leads execution of cross-functional initiatives. • Effectively utilizes project management tools/techniques to drive multiple reputed company; responsible for overall project management for several reputed company simultaneously. • Works with cross-functional project teams to reputed company project objectives, strategies, corresponding timelines, and milestones. • Coordinates activities and communications on writing reputed company/submissions utilizing cross-functional skills/expertise and drug development knowledge. • Holds team members to the project tasks/deliverables. Requirements: • A minimum of 8 years of bio-pharmaceutical industry experience in global reputed company, biotech, life science, or reputed company authority delivering medicines/therapies to a broad market across various therapeutic areas. • Minimum of 2-3 years of people management experience. • Bachelor's Degree or higher required; scientific discipline preferred • Possesses broad knowledge and reputed company record of successfully managing a clinical and regulatory writing group. • Proactively prepares for reputed company possible document obstacles. • Demonstrated high level of competency in the reputed company leadership behaviors. • Big picture and strategic thinker – can formulate a reputed company of reputed company state and reputed company the organization to build tactical plans to reputed company this. • Experience implementing large-reputed company change and process improvements relating to clinical and regulatory writing. • Builds relationships and reputed company cross functional alignment. • Experience with cross-functional leadership and a proven ability to influence and get things done reputed company the intricacies of a highly matrixed organization. • Excellent business and financial aptitude, reputed company analytical and uses data to drive the business and reputed company improvements. • Experience leading scaled global teams; managing and developing talent; leader who is reputed company to engage, reputed company, and reputed company large, diverse teams of seasoned professionals. Benefits: • reputed company time off (vacation, holidays, reputed company) • medical/dental/reputed company insurance • 401(k) to eligible employees • long-term incentive programs Apply tot his job Apply To this Job