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Director, Project Management

Job in Nashville, Davidson County, Tennessee, 37247, USA
Listing for: August Bioservices, LLC
Full Time position
Listed on 2026-02-16
Job specializations:
  • Management
    Program / Project Manager, Operations Manager
Salary/Wage Range or Industry Benchmark: 125000 - 150000 USD Yearly USD 125000.00 150000.00 YEAR
Job Description & How to Apply Below

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The Director of Project Management coordinates all projects related to client programs spanning across pre-formulation, formulation development, analytical development, cGMP manufacturing and stability studies for drug product development from preclinical to commercial. The Director of Project Management serves as the leader of the project management platform driving continuous improvement, by providing strategic direction, setting clear expectations and employing performance metrics to track delivery against client expectations.

This role is accountable for managing our client programs internally and directly engaging with our clients throughout the life of the program. This position requires a scientific background with global expertise in current Good Manufacturing Processes (GMP), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), a comprehensive understanding of the drug development lifecycle and of clinical and commercial pharmaceutical manufacturing.

The CDMO environment is fast-paced and requires an elevated level of multi-tasking skills that is essential to the success of this position.

The Director of Project Management coordinates all projects related to client programs spanning across pre-formulation, formulation development, analytical development, cGMP manufacturing and stability studies for drug product development from preclinical to commercial. The Director of Project Management serves as the leader of the project management platform driving continuous improvement, by providing strategic direction, setting clear expectations and employing performance metrics to track delivery against client expectations.

This role is accountable for managing our client programs internally and directly engaging with our clients throughout the life of the program. This position requires a scientific background with global expertise in current Good Manufacturing Processes (GMP), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), a comprehensive understanding of the drug development lifecycle and of clinical and commercial pharmaceutical manufacturing.

The CDMO environment is fast-paced and requires an elevated level of multi-tasking skills that is essential to the success of this position.

ESSENTIAL DUTIES & RESPONSIBILITIES
  • Provides operational leadership for customer projects in drug development and manufacturing
  • Actively engages in and supports new business development opportunities
  • Ensures timely and effective communication with business partners and leadership teams
  • Manages a team of PMs who are directly assigned as the primary liaison for specific client programs
  • Prepares meeting agendas, manages, and leads meetings, tracks action items via meeting minutes, and coordinates team activities through use of project management tools
  • Develops a communication plan that will ensure alignment amongst the project team, client, internal subject matter experts, and all stakeholders
  • Fosters a positive client experience and relationship, by providing industry leading customer service
  • Establishes and manages project scope and work plans
  • Ensures collaboration with appropriate team members across different functions for driving business decisions and client communication
  • Manages changes in scope of projects through change orders
  • Works closely with extended team to ensure project deliverables meet customer expectations and timelines
  • Manages multiple client projects ensuring on-time, within-budget delivery.
  • Accountable for hosting client visits to site. Ensures that all personnel involved with these activities on site are fully briefed regarding the nature of the visit, the customer, and their business interests
KNOWLEDGE, SKILLS, & ABILITIES
  • A bachelor’s degree in science or engineering required; master’s degree and/or PMP preferred.
  • Experience (10+ years) managing cross-functional teams or projects in a CDMO or pharmaceutical development or manufacturing setting
  • Knowledge of project management techniques and tools
  • Excellent leadership, written and verbal communication skills and ability to…
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