Center Manager
Springfield, IL · On-site
Onsite Contract Duration: Hiring Pay Range Min: 79,200.00 Hiring Pay Range Max: 118,200.00 Center ... Ensure compliance with FDA, CLIA, cGMP, SOPs, and other regulatory requirements. * Lead, develop ...
Springfield, IL · On-site
Onsite Contract Duration: Hiring Pay Range Min: 79,200.00 Hiring Pay Range Max: 118,200.00 Center ... Ensure compliance with FDA, CLIA, cGMP, SOPs, and other regulatory requirements. * Lead, develop ...
Springfield, IL · On-site
Onsite Contract Duration: Hiring Pay Range Min: 79,200.00 Hiring Pay Range Max: 118,200.00 Center ... Ensure compliance with FDA, CLIA, cGMP, SOPs, and other regulatory requirements. * Lead, develop ...
Springfield, IL · On-site
Contract Duration: Hiring Pay Range Min: Hiring Pay Range Max: Donor Floor Lead KEDPLASMA is a ... Ensure procedures are conducted in compliance with SOPs and FDA guidelines. * Troubleshoot ...
Springfield, IL · On-site
Contract Duration: Hiring Pay Range Min: Hiring Pay Range Max: Donor Floor Lead KEDPLASMA is a ... Ensure procedures are conducted in compliance with SOPs and FDA guidelines. * Troubleshoot ...
$40.6K - $49.5K
1% of jobs
$49.5K - $58.3K
3% of jobs
$58.3K - $67.1K
4% of jobs
$67.1K - $76K
5% of jobs
$76K - $84.8K
7% of jobs
$88.9K is the 25th percentile. Wages below this are outliers.
$84.8K - $93.6K
8% of jobs
$93.6K - $102.4K
7% of jobs
$102.4K - $111.3K
7% of jobs
The median wage is $112.3K / yr.
$111.3K - $120.1K
48% of jobs
$120.1K - $128.9K
4% of jobs
$128.9K - $137.8K
3% of jobs
$40.6K
$105.1K
$137.8K
An FDA Contract job refers to a temporary or project-based position working with or for the U.S. Food and Drug Administration (FDA) through a contractual agreement. These roles can be with the FDA directly or through third-party contractors supporting FDA initiatives. Responsibilities may include regulatory compliance, data analysis, scientific research, IT support, or administrative tasks. Contract positions vary in duration and benefits but provide opportunities to work in a highly regulated environment.
As an FDA Contract professional, your primary responsibilities usually include developing, reviewing, and managing documents and agreements in accordance with FDA guidelines and regulations. You may coordinate closely with regulatory affairs, legal, and project management teams to ensure that all contract terms support compliance and meet project timelines. Daily tasks might involve drafting and negotiating contract language, tracking deliverables, and supporting regulatory submissions. This role is both detail-oriented and collaborative, and it provides valuable experience for those seeking advancement into regulatory management or specialist positions.
To thrive in an FDA Contract role, you need strong knowledge of FDA regulations, compliance processes, and contract management, often supported by a background in life sciences or regulatory affairs. Familiarity with tools such as Document Control Systems, eCTD publishing software, and experience with regulatory submission platforms are typically required. Outstanding attention to detail, negotiation skills, and the ability to collaborate across cross-functional teams help candidates excel. These competencies are critical for ensuring contracts meet strict regulatory standards and for navigating the complexities of FDA approval and compliance procedures.
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 16 days ago