1

Pharma Project Manager Jobs in Reston, VA (NOW HIRING)

What You'll Do * Manage document lifecycle processes * Oversee turnover packages and readiness ... Experience on large capital pharma/biotech or advanced manufacturing projects Location: East Coast ...

Manager, Analytical R&D

Chantilly, VA · On-site

$100K - $130K/yr

... pharma company in the US! With our sites in Chantilly and Manassas, Virginia, we have R&D through ... Use project management techniques to identify, develop and maintain planning tools (e.g ...

Procurement Manager

Germantown, MD · On-site

$100 - $125/hr

Supplier Relationship Management (SRP), and 5+ yrs of Pharma experience, Biotech preferred * 5+ ... Strong negotiation, analytical, project management skills and familiarity with global sourcing and ...

You have experience working across science and education - with biotech, pharma, and academic ... A minimum 7 years project management experience * Registered Architect * Must have experience on ...

Procurement Manager

Germantown, MD · On-site

$90K - $120K/yr

Supplier Relationship Management (SRP), and 5+ yrs of Pharma experience, Biotech preferred * 5+ ... Strong negotiation, analytical, project management skills and familiarity with global sourcing and ...

You have experience working across science and education - with biotech, pharma, and academic ... A minimum 7 years project management experience * Registered Architect * Must have experience on ...

Showing results 41-60

Pharma Project Manager information

See Reston, VA salary details

$22

$48

$79

How much do pharma project manager jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for pharma project manager in Reston, VA is $48.11, according to ZipRecruiter salary data. Most workers in this role earn between $41.78 and $52.79 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.

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 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.

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.

How much do pharmaceutical project managers make in the US?

Pharmaceutical project managers in the US typically earn between $90,000 and $130,000 annually, with salaries varying based on experience, location, and company size. Senior roles or those with specialized skills and certifications can earn higher compensation, often exceeding $150,000 per year.

What are popular job titles related to Pharma Project Manager jobs in Reston, VA?

For Pharma Project Manager jobs in Reston, VA, the most frequently searched job titles are:

What job categories do people searching Pharma Project Manager jobs in Reston, VA look for?

The top searched job categories for Pharma Project Manager jobs in Reston, VA are:

What cities near Reston, VA are hiring for Pharma Project Manager jobs?

Cities near Reston, VA with the most Pharma Project Manager job openings:

Infographic showing various Pharma Project Manager job openings in Reston, VA as of August 2026, with employment types broken down into 85% Full Time, 14% Part Time, and 1% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $100,066 per year, or $48.1 per hour.

Sr. R&D Scientist

Manassas, VA • On-site

Catalent Pharma Solutions
Pharmaceutical Product Wholesalers • 10K+ employees

Full-time

Medical, Dental, Vision, PTO

Posted 28 days ago


Key responsibilities

  • Plan, coordinate, and guide the development and evaluation of new products, including pre-formulation excipient selection, compatibility studies, formulation development, process optimization, and scale-up manufacturing

  • Provide technical leadership and mentoring to individuals, functional areas, and the organization as required

  • Ensure appropriate technical review and oversight for portfolio projects and programs


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

61st of 86 rated pharmaceutical


Job description

About Site

The ~70,000squarefoot Manassas facility operates within Catalent's Consumer Health portfolio, supporting programs from early development through commercial manufacturing and packaging. It is designed for dietary supplement and foodsafety cGMP operations, making it distinct from Catalent's traditional pharmaceutical and biologics manufacturing sites.

Position Summary

We have an opportunity for a Senior R&D Scientist to join our team and provide technical direction and expertise throughout the entire product development process. This role focuses on pre-formulation studies, process optimization, and stability studies. You will define development studies, author and approve protocols and reports, and interpret analytical results for formulation development. You will also provide technical expertise and support on multiple projects while maintaining a Patient/Consumer First culture.

Shift: Monday to Friday 9am-5:30pm
Location: Manassas, VA
100% Onsite

The Role

  • Plan, coordinate, and guide the development and evaluation of new products, including pre-formulation excipient selection, compatibility studies, formulation development, process optimization, and scale-up manufacturing

  • Provide technical leadership and mentoring to individuals, functional areas, and the organization as required

  • Ensure appropriate technical review and oversight for portfolio projects and programs

  • Communicate effectively and on time with management, other departments, and customers regarding development activities, results, and next steps

  • Operate under and maintain Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) conditions and practices

  • Maintain and improve compliance with training, best practices, safety, and cleaning requirements

  • Represent functional area and projects by leading discussions at local, technical, governance, executive, and customer meetings

  • Lead Catalent's strategies, initiatives, expectations, processes, and portfolio commitments

  • Work extended hours and weekends as needed, especially when problems occur or deadlines must be met

  • Perform other duties as required

The Candidate

Minimum Requirements

  • Bachelor's degree in science or related field

  • Minimum 5-7 years of experience in a formulation role in a lab setting

  • Minimum of 3-5 years of experience with soft confectionery formats, particularly chew and/or lozenge formats

  • Experience working in a dietary supplement, confection, and/or pharmaceutical manufacturing and/or GMP facility

  • Expertise in soft chew and lozenge technologies for dietary supplement development

  • Excellent time management and organizational skills

  • Experience in troubleshooting and problem solving

  • Proficiency in Microsoft Office

  • Strong interpersonal skills to work effectively with people at all levels and in various functional areas; ability to influence and motivate others to achieve results

  • While performing the responsibilities of the job, the employee is required to talk and hear. The employee is often required to sit and use their hands and fingers to handle or feel and to manipulate keys on a keyboard. Use of manual dexterity is required. The employee is occasionally required to stand, walk, reach with arms and hands, bend or twist, and to stoop, kneel, crouch, or crawl. Vision abilities required by this job include close vision.

Preferred Skills & Background

  • Master's degree preferred

Why You Should Join Catalent

  • Positive and fast-paced working environment focusing on continually improving processes to remain innovative and dynamic

  • Competitive Paid Time Off plus 8 paid holidays

  • Medical, dental, and vision benefits effective day one of employment

  • Tuition Reimbursement - support to finish your degree or earn a new one

  • Site-based Employee Engagement activities such as potlucks, cookouts, and monthly birthday recognitions

  • Employee Resource Groups focusing on Diversity and Inclusion

  • Environmentally friendly, community engagement green initiatives

  • Defined career path and annual performance review process with potential for career growth

  • WellHub program to promote overall physical and mental wellness

  • Perkspot - exclusive discounts from over 900 merchants in various categories

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


What Catalent employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Catalent logo

About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

Social media