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Contract Pharma Jobs in Reston, VA (NOW HIRING)

Precigen, Inc

Procurement Manager

Germantown, MD · On-site

$90K - $120K/yr

This role leads supplier selection, relationship management, and contract compliance while driving ... Supplier Relationship Management (SRP), and 5+ yrs of Pharma experience, Biotech preferred * 5+ ...

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Showing results 41-60

All JobsContract Pharma JobsContract Pharma Jobs in Reston, VA

Contract Pharma information

See Reston, VA salary details

$42.7K

$110.5K

$144.9K

How much do contract pharma jobs pay per year?

As of Aug 6, 2026, the average yearly pay for contract pharma in Reston, VA is $110,516.00, according to ZipRecruiter salary data. Most workers in this role earn between $92,800.00 and $124,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the contract pharma position, and why are they important?

To excel in Contract Pharma roles, candidates need a strong background in pharmaceutical sciences, regulatory compliance, and project management, often supported by a degree in pharmacy, chemistry, or related fields. Familiarity with Good Manufacturing Practices (GMP), quality management systems, and industry-standard software such as LIMS or ERP platforms is typically required. Excellent communication, organizational abilities, and problem-solving skills help professionals manage client relationships and coordinate complex projects. These skills are critical for ensuring high-quality service delivery, compliance with regulations, and successful collaboration in a fast-paced, client-driven environment.

What are the typical day-to-day responsibilities for someone working in a contract pharma role?

In a Contract Pharma position, your day-to-day tasks often involve coordinating with internal teams and external clients to manage project timelines, ensure compliance with industry regulations, and oversee the progress of drug development or manufacturing contracts. You may also be responsible for preparing documentation, monitoring the quality of outputs, and troubleshooting issues that arise during production or delivery. Collaboration is a significant aspect of the role, as you will work closely with R&D, quality assurance, and regulatory affairs departments to meet project milestones. The environment is dynamic, with shifting priorities based on client needs and industry developments, making adaptability and strong organizational skills essential.

What is a contract pharma?

A Contract Pharma job typically involves working for a contract development and manufacturing organization (CDMO) that provides outsourced services to pharmaceutical companies. These roles can include research and development, manufacturing, quality control, regulatory compliance, and packaging. Employees in this field help pharmaceutical companies bring drugs to market efficiently while ensuring compliance with industry regulations. Contract Pharma professionals work with multiple clients, offering expertise in drug formulation, scale-up, and commercialization.

What are the most commonly searched types of Pharma jobs in Reston, VA? The most popular types of Pharma jobs in Reston, VA are:
What job categories do people searching Contract Pharma jobs in Reston, VA look for? The top searched job categories for Contract Pharma jobs in Reston, VA are:
What cities near Reston, VA are hiring for Contract Pharma jobs? Cities near Reston, VA with the most Contract Pharma job openings:
Contract Pharma jobs near you
Infographic showing various Contract Pharma job openings in Reston, VA as of July 2026, with employment types broken down into 55% Full Time, 18% Part Time, 1% Temporary, and 26% Contract. Highlights an 74% Physical, 2% Hybrid, and 24% Remote job distribution, with an average salary of $110,516 per year, or $53.1 per hour.

Head of Clinical Operations ( On site role)

Precigen, Inc

Germantown, MD • On-site

Full-time

Re-posted 18 days ago

Job description

Precigen is seeking a highly motivated and skilled Head of Clinical Operations (level determined by candidate experience), to drive our clinical trial programs to develop next generation gene and cell therapies focused in immuno-oncology, autoimmune disorders, and infectious diseases. Reporting to the Head of Clinical Operations, this role is responsible for driving organizational strategy and overall execution of clinical program(s) to align with corporate objectives, collaborating with executive leadership and external stakeholders to drive the success of our clinical programs. The position will lead a high-performing Clinical Operation team to ensure work quality, timeliness and adherence to budget.

The candidate will have a strong knowledge of global regulatory guidelines, strong organization and time management skills, and demonstrate focus to output/deliverables.

DUTIES AND RESPONSIBILITIES:

  • Oversight of the execution of all clinical trials
  • Ensures all trials are conducted in accordance with applicable SOPs, ICH, GCP and other applicable regulations.
  • Responsibility for meeting timelines and the execution of clinical studies making sure deliverables, milestones, and budget parameters are met. Demonstrated ability to set and manage priorities, resources, performance targets and project initiatives in a global environment is required.
  • Manages resources and external vendors efficiently
  • Responsible for overall budget forecasting and management
  • Maintains and provides relevant and accurate information for monthly study reports (including enrollment curves, timelines, analysis of the study status and identification of potential risks) Clinical Trial material (CTM) Management, budget, and finances, change orders, contracts.
  • Provide Clinical Operations expertise in cross-functional meetings and works closely with cross functional members to ensure the quality and in accordance with Precigen SOPs and global regulatory guidelines

EDUCATION AND EXPERIENCE:

  • PhD, MD or Bachelors in medical or life science, regulatory science, or related field.
  • Strong understanding of global regulatory guidelines and processes.
  • Minimum of ten (10)+ years progressive experience in pharma/biopharma clinical operations.
  • Experience with biologics/gene therapy is preferred.

DESIRED KEY COMPETENCIES:

  • Ability to understand and execute on the company’s mission and values.
  • Exceptional organization skills with strong attention to detail.
  • Strong personal leadership and self-direction.
  • Clear communication in both oral and written form.
  • Demonstrated ability to work with and coordinate demands from multiple stakeholders.
  • Exhibition of the highest degree of ethical standards and trustworthiness.
  • Advanced skills in Microsoft Word, Adobe Acrobat Professional®, and clinical trial management systems (CTMS).