
Associate Director – Project Management
Posted Sep 1

Posted Sep 1
This is a fully remote position, open to applicants in North Carolina.
• Support and oversee large, multinational projects.
• Manage significant national or global projects, programs of projects, and complex initiatives related to customer deliverables.
• Provide functional leadership, supervision, support, training, and mentorship to Project Managers.
• Oversee project/program delivery, ensuring adherence to cost, time, and quality requirements across various divisions.
• Lead core project teams and facilitate the leadership of extended project teams.
• Coordinate internal and external cross-unit collaboration, including subcontractors.
• Define and manage project resource requirements and contingency plans.
• Design, implement, monitor, and adjust project plans as necessary.
• Foster effective teamwork and mediate conflicts.
• Communicate project-related issues with PM Management.
• Achieve financial performance targets for assigned clinical projects.
• Ensure project deliverables align with company and client expectations.
• Initiate enhancements to improve efficiency and quality.
• Act as the primary client contact for designated projects and clients.
• Cultivate relationships with client project teams and vendors.
• Ensure staff compliance with professional standards and clinical research SOPs.
• Collaborate with Business Development and Bids/Contracts on client presentations and proposals.
• Assist in resource utilization, policy formulation, and goal implementation.
• Prepare and potentially conduct performance evaluations and salary assessments.
• Execute other responsibilities as assigned by management.
• Bachelor's or college degree (preferably in life sciences) or certification in a related allied health field from a recognized institution (e.g., nursing certification, medical technology, or laboratory technology), or an equivalent mix of education and experience.
• At least eight (8) years of experience in the clinical pharmaceutical industry, demonstrating skills and competence in clinical project management tasks.
• Alternatively, over five (5) years of supervisory experience in a healthcare environment and six (6) years of clinical research experience within the pharmaceutical or CRO industry.
• Proven success in clinical development and in leading and developing professional staff in a project-focused environment.
• Demonstrated experience in developing and managing budgets and resources for a segment of the business.
• Proficient in project management software.
• Experience in conducting global clinical trials.
• Willingness to travel domestically and internationally, including overnight stays.
• Possession of a valid passport.
• Capability to drive with a valid driver's license.
• Proficient in both the local office language and English, in written and verbal forms.
• Broad understanding of the drug development process and client requirements.
• Strong leadership capabilities.
• Solid financial understanding.
• Excellent judgment and decision-making abilities.
• Effective oral and written communication skills, including proficiency in English.
• Exceptional interpersonal skills and problem-solving aptitude.
• Strong organizational and negotiation abilities.
• Expert knowledge of project management principles and their applications.
• Familiarity with budgeting, forecasting, and resource management.
• Ability to function effectively in matrix organizations.
• Understanding of multicultural service organizations.
• Awareness of regulatory guidelines and directives.
• Skills in process improvement, particularly in clinical trials, clinical development, and project management.
• Knowledge of medical therapeutic areas and medical terminology.
• Strong marketing and negotiation skills.
• Proficient computer skills.
• Competitive benefits package based on location.
• Transparent compensation and pay equity.
• Opportunities for domestic and international travel, including overnight stays.
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