Director Pbmc information
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$24.1K - $37.2K
6% of jobs
$41.4K is the 25th percentile. Wages below this are outliers.
$37.2K - $50.3K
57% of jobs
$61.7K is the 75th percentile. Wages above this are outliers.
$50.3K - $63.4K
13% of jobs
$63.4K - $76.5K
3% of jobs
$76.5K - $89.5K
4% of jobs
$89.5K - $102.6K
6% of jobs
$102.6K - $115.7K
3% of jobs
$115.7K - $128.8K
5% of jobs
$128.8K - $141.9K
1% of jobs
$141.9K - $155K
0% of jobs
How much do director pbmc jobs pay per year?
As of Sep 1, 2026, the average yearly pay for director pbmc in the United States is $63,209.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,500.00 and $84,000.00 per year, depending on experience, location, and employer.
A Director PBMC (Peripheral Blood Mononuclear Cell) is a senior-level professional responsible for overseeing the operations, management, and strategic direction of laboratories or facilities that process and manage PBMCs. These cells are crucial for clinical research, immunology, and pharmaceutical studies. The Director PBMC ensures compliance with regulatory standards, manages staff, coordinates with research teams, and helps develop protocols for PBMC isolation, storage, and distribution. This role is vital for supporting research in immunotherapies, vaccine development, and other biomedical fields.
To thrive as a Director PBMC, you need a robust background in immunology or cellular biology, advanced degrees (such as a PhD or MSc), and significant laboratory management experience. Expertise with flow cytometry, cell sorting, LIMS, and regulatory compliance (such as GLP/GMP) is typically required, along with relevant certifications. Outstanding leadership, project management, and interpersonal skills help drive team performance and foster external collaborations. Mastery of these skills ensures high-quality PBMC processing, regulatory adherence, and successful research or clinical outcomes.
A Director PBMC often encounters challenges related to maintaining the quality and consistency of PBMC isolation and storage processes, especially when handling large-scale or multi-site clinical studies. They must ensure compliance with strict regulatory standards and oversee training to maintain technical proficiency within their team. Additionally, effective communication and collaboration with clinical staff, project managers, and quality assurance teams are crucial for troubleshooting issues and meeting project deadlines. Successfully balancing these responsibilities is key to supporting research outcomes and advancing the organization's scientific goals.
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