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
• Must have 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 Number: 42026