Associate Director, Project Management

Associate Director, Project Management, Denville, NJ: Analyze and coordinate the timelines, procurement, schedules, staffing, among others per project basis. Lead and develop a talented Project Management team, ensuring they have the required skills and resources to excel in their roles. Establish and maintain a robust PMO, promoting industry-leading Project Management practices and a collaborative culture. Provide thought leadership, training, and mentorship to project managers, fostering a uniform approach to project delivery. Collaborate with the leadership team to integrate project management with site operations, driving the realization of our strategic plan. Monitor project status, ensuring timely delivery within budget and scope. Foster a customer-centric approach, integrating client relationship management with project governance to achieve exceptional results. Manage individual projects, identifying and mitigating risks, and developing solutions that meet customer expectations. Define, track, and communicate key performance indicators (KPIs), and ensure budget management aligns with company financial goals. Develop and maintain a comprehensive revenue forecast, working closely with the Business Development team and project managers. Address escalated project issues, coordinating solutions to ensure project delivery and maintaining CSI score deliverables. Regularly provide project portfolio reports to senior management, highlighting budget and schedule variances, risks, and status. The position will supervise one employee. Requirements: Applicant must have a Master’s degree (or US Equivalent) in Project Management, Health Administration, Pharmaceutical Science or related field and two (2) years of experience in project management environment within pharmaceutical or biotech industry. Proven experience in drug development processes, Analytical R&D, CMC, and regulatory pathways. Must have demonstrated experience with PRINCE2, PMP and delivering large complex projects within time and financial budget. Applicant must have strong analytical and problem-solving skills, ability to identify and mitigate risks, lead and develop high performing project management teams. PMP certification is required. 40 hours per week. M-F: 9:00 a.m. to 5:00 p.m. Must have proof of legal authority to work in the United States. Salary: $126,610-145,000 per year. To be considered, please visit RiconPharma LLC’s, an Ingenus Pharmaceuticals affiliate, career site website at https://www.ingenus.com/careers/ and apply by emailing your resume to hr@ingenus.com . Job#42026