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Clinical Operations Jobs in Reston, VA (NOW HIRING)

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Clinical Operations information

See Reston, VA salary details

$36.4K

$102K

$194K

How much do clinical operations jobs pay per year?

As of Sep 9, 2026, the average yearly pay for clinical operations in Reston, VA is $101,995.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,400.00 and $118,100.00 per year, depending on experience, location, and employer.

What is clinical operations?

Clinical operations refers to the planning, management, and execution of clinical trials and research studies within the healthcare and pharmaceutical industries. Professionals in clinical operations ensure that studies are conducted efficiently, ethically, and in compliance with regulatory requirements. Their responsibilities may include site management, patient recruitment, data collection, and ensuring protocol adherence. The goal is to facilitate the safe and effective development of new medical treatments and therapies.

How does a clinical operations professional typically collaborate with cross-functional teams during a clinical trial?

Clinical Operations professionals play a central role in coordinating activities among various teams such as regulatory affairs, data management, biostatistics, and clinical research associates. They ensure that timelines are met, protocols are followed, and all departments are aligned with trial objectives. Regular meetings, clear communication, and the ability to anticipate and resolve operational challenges are essential to successful collaboration. This cross-functional teamwork helps maintain trial quality and regulatory compliance throughout the study.

What are the key skills and qualifications needed to thrive in clinical operations, and why are they important?

To thrive in Clinical Operations, you need expertise in clinical trial management, regulatory compliance, and data analysis, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) certification, and electronic data capture (EDC) platforms is essential. Strong leadership, problem-solving, and communication skills help coordinate teams and ensure project timelines are met. These skills are crucial for guaranteeing efficient, compliant, and successful clinical trial execution in a highly regulated environment.

What is the difference between Clinical Operations vs Clinical Research Associate?

AspectClinical OperationsClinical Research Associate
Required CredentialsBachelor's degree, experience in clinical trial managementBachelor's degree, often with certification in clinical research
Work EnvironmentProject management, coordinating multiple trial sitesMonitoring clinical sites, ensuring protocol compliance
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, pharmaceutical companies
Common Search & ComparisonFocuses on trial oversight and managementFocuses on site monitoring and data verification

Clinical Operations professionals oversee the planning, coordination, and management of clinical trials, ensuring they run smoothly across multiple sites. Clinical Research Associates primarily monitor clinical trial sites, verify data accuracy, and ensure compliance with protocols. While both roles require knowledge of clinical research, Clinical Operations has a broader scope involving project management, whereas CRAs focus on site-level monitoring.

What are the most commonly searched types of Clinical Operations jobs in Reston, VA?

The most popular types of Clinical Operations jobs in Reston, VA are:

What cities near Reston, VA are hiring for Clinical Operations jobs?

Cities near Reston, VA with the most Clinical Operations job openings:

Infographic showing various Clinical Operations 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 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $101,995 per year, or $49 per hour.

Head of Clinical Operations ( On site role)

Germantown, MD • On-site

Precigen, Inc
Biotechnology Research and Development • 51 - 200 employees

Full-time

Re-posted 23 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).