Cell & Gene Therapy SME - US

PPG US ProPharma Group, LLC

Raleigh (NC)

Hybrid

USD 110,000 - 170,000

Full time

4 days ago
Be an early applicant
Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Job summary

ProPharma Group is seeking a senior CGT Project Manager to oversee product development and analytical transfer projects. You will coordinate planning, execution, and communication across client teams and internal stakeholders, ensuring on-time delivery and quality.

The role requires deep CGT process knowledge, GMP/ISO familiarity, and strong leadership in a hybrid work environment. The ideal candidate has 10+ years in CGT project management, excellent presentation and analytical skills, and a

Qualifications

  • Demonstrated knowledge of the overall drug development process relevant to CGT operations.
  • Demonstrated knowledge of Good Manufacturing Practices and ISO relevant to CGT.
  • Advanced understanding and proficiency with PowerPoint, Word, Excel, Visio, Project, OneDrive, and SharePoint.
  • Good proficiency with project management practices, tools, and methodology.
  • Excellent analytical skills and ability to resolve difficult business situations and communicate complex issues clearly.
  • Ability to organize and manage multiple projects and present persuasively.
  • Willingness to travel.

Responsibilities

  • Demonstrate subject matter expertise in CGT project delivery across development and transfer.
  • Oversee planning, delivery, and communication of CGT projects.
  • Facilitate meetings, ensure stakeholder alignment, and manage project financials.
  • Develop project deliverables and conduct reviews with client leadership.
  • Drive status reporting and risk mitigation across projects.
  • Support staffing and resource recommendations for client projects.

Skills

CGT knowledge
Project management
Communication
Analytical skills
Presentation skills

Education

B.S./B.A. in Life Sciences
Advanced degree in scientific discipline

Tools

PowerPoint
Word
Excel
Visio
Project
OneDrive
SharePoint

Job description

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Essential Functions
  • Demonstrate subject matter expertise in Cell and Gene Therapies (CGT) (e.g., product development, analytical methos development and transfer, facility startup and qualification, project management, process improvements, etc.) through the delivery of CGT projects.
  • Oversee or drive planning, delivery, communication, and operational / tactical aspects of the project(s).
  • Work independently with limited oversight from senior leadership.
  • Facilitate project team meetings, cross-functional communication and decision making, ensuring alignment with internal and external stakeholders.
  • Oversee and manage project financials.
  • Prepare project team budget including resources and costs, collaborating with Finance and other cross-functional departments.
  • Evaluate budget compliance and project billings on an ongoing basis.
  • Develop all project deliverables (e.g., project plan, charter, communication plans, presentations) and conduct reviews / approvals with client leadership.
  • Drive project communication (e.g., status reports, dashboards) to all impacted stakeholders.
  • Effectively conduct face-to-face and virtual ongoing meetings and workshops.
  • Own quality of work and most, if not all, deliverables under your responsibility.
  • Manage scope and monitor progress of project activities.
  • Proactively identify risks and issues in a timely manner, collaborate with colleagues and client lead(s) to resolve issues, and adjust project plans as needed.
  • Responsible for the schedule and quality of assigned projects, if applicable.
  • Support the project sales process with Business Development by developing content, reviewing content, and participating in sales meetings.
  • Support staffing client projects by identifying / recommending resources, conducting resume reviews, and interviewing resources, as requested.
  • Support the development of the Marketing and Sales plans and materials (e.g., thought capital, webinars) for CGT for the fiscal year.
  • Understand and track CGT-related industry trends; determine how to leverage for clients and turn into potential service offerings.
  • Participate in and present at industry associations and information exchanges related to development of related guidance and practice.
  • Ensure performance management processes (e.g., goal setting, performance evaluations) for personnel are completed in a timely manner.
  • Carry out supervisory responsibilities in accordance with the organization’s policies and applicable guidelines.
  • Participate in internal or client-required staff training.
  • Enforce Human Resources policies and procedures with the support of Human Resources staff.
  • Other duties as assigned.
Necessary Skills and Abilities
  • Demonstrated knowledge of the overall drug development process relevant to CGT operations.
  • Demonstrated knowledge of Good Manufacturing Practices and ISO relevant to CGT.
  • Advanced understanding and proficiency with utilizing PowerPoint, Word, Excel, Visio, Project, OneDrive, and SharePoint.
  • Good proficiency with project management practices, tools, and methodology.
  • Excellent analytical skills: (1) ability to access and resolve difficult business situations; (2) communicate complex issues in a simple manner.
  • Ability to organize and manage multiple projects.
  • Ability to make effective and persuasive presentations.
  • Excellent interpersonal skills, ability to develop important relationships with customers and key stakeholders, good conflict management skills.
  • Able to work effectively with local and virtual team members and other professionals.
  • Ability to earn and maintain a client’s confidence through appropriate planning, organizing, controlling, and directing of a project.
  • Proven track record of good decision making and exercising sound judgment.
  • Drive to Completion: Ability to think ahead, take initiative, maintain confidentiality, prepare action plans, meet deadlines and work in a team environment.
  • Results and high attention to detail.
  • Able to organize and perform own work tasks independently.
  • Excellent communication skills - excellent written and oral English skills is a must, any other language is a plus.
  • Willingness to travel.
Necessary Skills and Abilities
  • Demonstrated knowledge of the overall drug development process relevant to CGT operations.
  • Demonstrated knowledge of Good Manufacturing Practices and ISO relevant to CGT.
  • Advanced understanding and proficiency with utilizing PowerPoint, Word, Excel, Visio, Project, OneDrive, and SharePoint.
  • Good proficiency with project management practices, tools, and methodology.
  • Excellent analytical skills: (1) ability to access and resolve difficult business situations; (2) communicate complex issues in a simple manner.
  • Ability to organize and manage multiple projects.
  • Ability to make effective and persuasive presentations.
  • Excellent interpersonal skills, ability to develop important relationships with customers and key stakeholders, good conflict management skills.
  • Able to work effectively with local and virtual team members and other professionals.
  • Ability to earn and maintain a client’s confidence through appropriate planning, organizing, controlling, and directing of a project.
  • Proven track record of good decision making and exercising sound judgment.
  • Drive to Completion: Ability to think ahead, take initiative, maintain confidentiality, prepare action plans, meet deadlines and work in a team environment.
  • Results and high attention to detail.
  • Able to organize and perform own work tasks independently.
  • Excellent communication skills - excellent written and oral English skills is a must, any other language is a plus.
  • Willingness to travel.
Educational Requirements

B.S./B.A. in the Life Sciences; advanced degree in scientific discipline is desired. Ten (10) years of relevant work experience may be substituted in lieu of education.

Experience Requirements

10 or more years’ multi-disciplinary experience in the CGT pharmaceutical and biotech industries. Minimum of 10 years’ direct project management in CGT. Experience using Project Management software to manage complex project timelines and resources. (MS Project or other PM Enterprise software). Experience in supporting sales activities of project services to clients. Supervisory experience, including employee hiring and retention, oversight, performance review, employee development, and discipline.

Diversity, Equity, Inclusion and Equal Opportunity
  • We celebrate our differences and strive to create a workplace where each person can be their authentic self.
  • We are committed to diversity, equity, and inclusion.
  • Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits.
  • With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
Remote/hybrid policy

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

Important Policy Information

ProPharma will never ask you for any bank account information, financial information, or another form of payment to be considered for a role.

Additionally, the ProPharma talent acquisition team will only use their work email addresses (domain@propharmagroup.com). If you receive recruiting communications from anyone with a yahoo.com, gmail.com, live.com, propharmagroupjobs.com, or any other email account, it’s likely a fraud.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Quality Specialist
Quality Specialist

ProPharma Group • Northern (KY)

Hybrid
USD 65,000 - 90,000
Remote work option
Hybrid work option
Equal Opportunity Employer
Director, Business Development
Director, Business Development

PPG US ProPharma Group, LLC • Raleigh (NC)

Hybrid
USD 90,000 - 130,000
Quality Specialist
Quality Specialist

ProPharma • Raleigh (NC)

Hybrid
USD 80,000 - 110,000
QA RA Director Consulting Position
QA RA Director Consulting Position

PPG US ProPharma Group, LLC • Raleigh (NC)

Hybrid
USD 180,000 - 240,000
QA RA Director Consulting Position
QA RA Director Consulting Position

ProPharma • Raleigh (NC)

Hybrid
USD 130,000 - 180,000
Senior Clinical Line Manager
Senior Clinical Line Manager

PPG US ProPharma Group, LLC • Raleigh (NC)

Hybrid
USD 120,000 - 180,000
Director, Business Development
Director, Business Development

ProPharma • Raleigh (NC)

Hybrid
USD 90,000 - 130,000
Remote-friendly policies
Hybrid work model
Travel opportunities
Research Assistant
Research Assistant

ProPharma Group • Northern (KY)

Hybrid
USD 40,000 - 52,000
Research Assistant
Research Assistant

PPG US ProPharma Group, LLC • Raleigh (NC)

Hybrid
USD 42,000 - 60,000
Clinical Project Specialist
Clinical Project Specialist

ProPharma • Raleigh (NC)

On-site
USD 65,000 - 90,000