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Pharma Project Manager Jobs in Tennessee (NOW HIRING)

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... August is seeking a Project Manager - Operations to join our growing Project Management ...

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... August is seeking a Project Manager - Operations to join our growing Project Management ...

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... August is seeking a Project Manager - Operations to join our growing Project Management ...

IT Project Manager

Clarksville, TN ยท On-site

$85K - $101K/yr

IT Project Manager Contract: 12 Months Onsite Local Candidates Nashville, TN Seeking an experienced ... tobacco, pharma, CPG) strongly preferred โ€ข Exceptional stakeholder management and executive ...

IT Project Manager

Nashville, TN ยท On-site

$80.29/hr

Onsite Job We are seeking an experienced IT Project Manager to lead the delivery of technology ... G., tobacco, pharma, Client) strongly preferred โ€ข Exceptional stakeholder management and ...

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... Expected to be able to present own work to peers and cross-functional managers and influence ...

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... Expected to be able to present own work to peers and cross-functional managers and influence ...

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... Expected to be able to present own work to peers and cross-functional managers and influence ...

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Pharma Project Manager information

See Tennessee salary details

$19

$41

$69

How much do pharma project manager jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for pharma project manager in Tennessee is $41.97, according to ZipRecruiter salary data. Most workers in this role earn between $36.44 and $46.06 per hour, depending on experience, location, and employer.

What does a Pharma Project Manager do?

A Pharma Project Manager oversees and coordinates pharmaceutical projects, ensuring they are completed on time, within scope, and on budget. This role involves managing cross-functional teams, planning project timelines, handling risks, and ensuring compliance with regulatory standards. Pharma Project Managers often work closely with research and development, clinical, regulatory, and manufacturing teams to bring new drugs or treatments to market efficiently and safely. Their responsibilities also include stakeholder communication and resource management throughout the project lifecycle.

What are the key skills and qualifications needed to thrive as a Pharma Project Manager, and why are they important?

To thrive as a Pharma Project Manager, you need strong project management expertise, knowledge of pharmaceutical regulations, and a background in life sciences or a related field. Familiarity with project management tools (such as Microsoft Project or Smartsheet), regulatory compliance systems, and certifications like PMP or PRINCE2 are commonly required. Exceptional organizational skills, problem-solving ability, and effective communication help you excel when coordinating cross-functional teams and managing complex timelines. These skills are crucial for ensuring projects are delivered on time, on budget, and in compliance with industry standards.

How does a Pharma Project Manager typically collaborate with cross-functional teams throughout a drug development project?

A Pharma Project Manager plays a central role in coordinating cross-functional teams, including research, clinical, regulatory, and manufacturing departments. They facilitate regular meetings, ensure clear communication of project goals, and address any obstacles that arise. Effective Pharma Project Managers build strong relationships with team members, align timelines, and manage resources to keep projects on track. This collaborative approach is essential for navigating the complexities of drug development and meeting regulatory and company milestones.

What is the difference between Pharma Project Manager vs Clinical Research Associate?

AspectPharma Project ManagerClinical Research Associate
CredentialsBachelor's or higher in life sciences, PMP certification often preferredBachelor's in life sciences, relevant clinical research certifications
Work EnvironmentCoordinates multiple projects across departments in pharmaceutical companiesMonitors clinical trial sites, ensuring protocol compliance
Employer & Industry UsagePharmaceutical companies, biotech firmsContract research organizations, clinical trial sites

While both roles are essential in the pharmaceutical industry, a Pharma Project Manager oversees multiple projects and teams, focusing on planning and execution, whereas a Clinical Research Associate primarily monitors clinical trial sites to ensure compliance and data integrity.

What are popular job titles related to Pharma Project Manager jobs in Tennessee? For Pharma Project Manager jobs in Tennessee, the most frequently searched job titles are:
What job categories do people searching Pharma Project Manager jobs in Tennessee look for? The top searched job categories for Pharma Project Manager jobs in Tennessee are:
What cities in Tennessee are hiring for Pharma Project Manager jobs? Cities in Tennessee with the most Pharma Project Manager job openings:
Infographic showing various Pharma Project Manager job openings in Tennessee as of July 2026, with employment types broken down into 83% Full Time, 15% Part Time, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $87,298 per year, or $42 per hour.
Project Manager

Project Manager

August Bioservices

Nashville, TN โ€ข On-site

Full-time

Posted 12 days ago


Job description

Headquartered in Nashville, TN - one of the fastest-growing and most exciting cities in the United States - August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project - including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August!
August is seeking a Project Manager - Operations to join our growing Project Management Organization! The Project Manager is a technically knowledgeable team member with proven abilities to support operations and customer project activities.
The Project Manager will be a hands-on with a passion for driving results in a customer centric environment. The successful candidate will strengthen August Bioservices Project Management operations and ensure that the company is providing superior levels of internal and external customer service. The Operations Project Manager will provide project leadership on internal initiatives that are strategic in nature, span across functional areas, provide practical and effective solutions for the business and will also coordinate activities related to drug discovery, pre-formulation, formulation development, analytical development, cGMP manufacturing and stability studies for drug product development from clinical to commercial manufacturing. The Project Manager will receive cross-functional assistance from each department to absorb and understand project variables within each business segment. The Operations Project Manager reports to the Director of Project Management who is responsible for providing operational leadership for operations and customer projects in drug discovery, drug development and manufacturing.
For this position, a scientific background with global experience in process improvement, current Good Manufacturing Processes (cGMP) and pharmaceutical manufacturing in a regulated environment is highly desired. The CDMO and CRO environment is fast-paced and requires an elevated level of multi-tasking skills that is essential to the success of this position. Internal partnerships are also a must as project managers will be required to learn and understand the capabilities of each business segment in collaboration with the rest of the organization to successfully drive project completion.
Responsibilities
  • Determine and maintain project timelines, estimated level of effort, and resource/budget requirements
  • Prioritize project activities , ensuring deadlines are achieved and the project team effectively communicates about progress and obstacles , both within the project team and to stakeholders
  • Manage and track all project related activities to ensure successful completion of objectives
  • Ensure that process improvements are both effective and durable by assisting process owners with training, documentation , and establishing process controls
  • Recognize and encourage behaviors that contribute to teamwork and improve outcomes , leveraging the unique talents of each project team
  • Prepares meeting agendas, manages and leads video/teleconferences, tracks action items via meeting minutes, and coordinates team activities as assigned.
  • Develops a communication plan that will ensure seamless communication with the project team, customer, project steering committee, and all stakeholders.
  • Actively engages in and supports new business development opportunities.
  • Manages changes in scope of projects by requests of change orders via Requests For Proposals.
  • Manages client relationships ensuring on-time project execution and 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 business enquiry, the customer and their business interests.
  • Build effective relationships throughout the organization and remove obstacles to success

Requirements
  • A Bachelor's Degree in scientific or engineering discipline required
  • Experience (5+ years) managing cross-functional teams or projects in a CDMO, pharmaceutical development, or GLP/GMP manufacturing setting, or analogous technical industry. 7-12 years preferred
  • Demonstrated experience in the use of process improvement methodologies, such as Lean or Six Sigma, or related practical approaches ( 5 Whys, 6 Ms , 7 Wastes, brainstorming, 2x2 prioritization matrix, Exploratory Data Analysis, etc. )
  • Ability to understand complex business processes and adapt solutions to meet the needs of the business
  • Proven analytical skills , with the ability to approach problem s logically and systematically
  • Knowledge and experience in the application of project management techniques and tools.
  • Excellent leadership, written and verbal communication skills and ability to influence others.
  • Excellent negotiation and facilitation skills, with strong customer-service focus.
  • Strong aptitude for technical comprehension enabling rapid learning in a highly regulated environment.
  • Ability to lead multi-disciplinary project teams.
  • Understanding of pharmaceutical product development and manufacturing.
  • Knowledge of FDA regulation/ICH guidelines, U.S. drug development process and project management practices preferred.
  • Proficiency in Microsoft Office programs including Word, Excel and MS Project.
  • Proficiency with Smartsheet, ERP, CRM, and Documentation Systems.

Success Factors
  • Must have exemplary interpersonal skills; should be an effective team leader who can manage and lead in a matrix environment.
  • Able to professionally handle multiple and sometimes competing priorities.
  • Thinks strategically. Quickly identifies and acts on opportunities.
  • Passion for customers. Listens to understand. Asks the right questions.
  • Communicates clearly to both internal and external customers in written and oral form.
  • Listens and responds positively to external customers, partners and colleagues at all levels.
  • Drives performance. Holds self and others accountable. Does not settle for status quo.
  • Prioritizes tasks according to business objectives and can pursue several objectives simultaneously, with a high attention to detail.
  • Proactively works with stakeholders to mitigate risks and overcome obstacles.
  • Makes and acts on decisions quickly. Makes decisions with the customer and patients in mind.
  • Meets commitments and timelines with a sense of urgency. Seeks ways to be more efficient.
  • Ability to adapt to a fast-paced environment.
  • Able to professionally handle multiple and sometimes competing priorities.
  • Excellent critical thinking and problem-solving skills.
  • Detailed and results orientated.

At August Bioservices, Our Credo is our culture. Everything we do, we do with great care. We believe in the promise of discovery and the power of science to transform lives. We assert that excellence is not a static destination, but a standard, and an every-day measuring stick of our advancement. We aspire to unlock the potential in every person, every process and every molecule - from start to finish. We are committed to doing the right thing the first time and every time, meeting or exceeding all regulatory requirements. We strive to be exceptional, preferred and indispensable partners for our customers; responsible and engaged citizens within our communities; and active, mindful stewards of our environment.
We are August Bioservices. We are pointing the way forward. If this sounds like your kind of working environment, we want you on our team!
August Bioservices is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.