Working knowledge of FDA guidelines and global regulatory expectations and their operational impact ... This is a remote opportunity open to candidates currently residing in the United States. IQVIA is a ...
Working knowledge of FDA guidelines and global regulatory expectations and their operational impact ... This is a remote opportunity open to candidates currently residing in the United States. IQVIA is a ...
Director, Pharmacovigilance Operations
Deerfield, IL · On-site +1
$210K - $250K/yr
This position reports to the VP of Pharmacovigilance and can be remote, hybrid or located at our ... Maintain readiness for FDA, Health Canada, partner, and internal audits. * Support regulatory ...
New
Director, Pharmacovigilance Operations
Deerfield, IL · On-site +1
$210K - $250K/yr
This position reports to the VP of Pharmacovigilance and can be remote, hybrid or located at our ... Maintain readiness for FDA, Health Canada, partner, and internal audits. * Support regulatory ...
New
Data Scientist II, Outcomes Research
Chicago, IL · On-site +1
$100K - $150K/yr
Hands-on experience contributing to regulatory submissions to the FDA or other health authorities ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...
Data Scientist II, Outcomes Research
Chicago, IL · On-site +1
$100K - $150K/yr
Hands-on experience contributing to regulatory submissions to the FDA or other health authorities ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...
Pharmacist Centralized Services Work From Home (Must Reside in LA)
Deerfield, IL · On-site +1
$59.25 - $71.25/hr
Responsible for prescription processing from a remote setting. Fosters strong relationships with ... Helps ensure area Pharmacies adhere to regulatory compliance, standard operating procedures and FDA ...
Pharmacist Centralized Services Work From Home (Must Reside in LA)
Deerfield, IL · On-site +1
$59.25 - $71.25/hr
Responsible for prescription processing from a remote setting. Fosters strong relationships with ... Helps ensure area Pharmacies adhere to regulatory compliance, standard operating procedures and FDA ...
Sr. Clinical Research Associate
Tennessee, IL · On-site +1
... remote). * Actively participate in site feasibility assessments and site selection processes. * Ensure study conduct is executed according to the clinical protocol, regulatory requirements (GCP, FDA ...
Sr. Clinical Research Associate
Tennessee, IL · On-site +1
... remote). * Actively participate in site feasibility assessments and site selection processes. * Ensure study conduct is executed according to the clinical protocol, regulatory requirements (GCP, FDA ...
Medical Science Liaison, Oncology - Great Lakes (IL, WI, MN, IA, MI, OH, MO)
Chicago, IL · On-site +1
This is a remote position open to applicants authorized to work for any employer within the United ... HIPPA and relevant FDA laws and regulations (certify completion where required). Basic ...
Medical Science Liaison, Oncology - Great Lakes (IL, WI, MN, IA, MI, OH, MO)
Chicago, IL · On-site +1
This is a remote position open to applicants authorized to work for any employer within the United ... HIPPA and relevant FDA laws and regulations (certify completion where required). Basic ...
TherOx SSO2 Therapy is the first FDA-approved therapy since the stent 20+ years ago to reduce ... For fully remote positions, compensation will comply with all applicable federal, state, and local ...
TherOx SSO2 Therapy is the first FDA-approved therapy since the stent 20+ years ago to reduce ... For fully remote positions, compensation will comply with all applicable federal, state, and local ...
Sr. Clinical Research Associate
Virginia, IL · On-site +1
... remote). * Actively participate in site feasibility assessments and site selection processes. * Ensure study conduct is executed according to the clinical protocol, regulatory requirements (GCP, FDA ...
Sr. Clinical Research Associate
Virginia, IL · On-site +1
... remote). * Actively participate in site feasibility assessments and site selection processes. * Ensure study conduct is executed according to the clinical protocol, regulatory requirements (GCP, FDA ...
Sr. Clinical Research Associate
Ohio, IL · On-site +1
... remote). * Actively participate in site feasibility assessments and site selection processes. * Ensure study conduct is executed according to the clinical protocol, regulatory requirements (GCP, FDA ...
Sr. Clinical Research Associate
Ohio, IL · On-site +1
... remote). * Actively participate in site feasibility assessments and site selection processes. * Ensure study conduct is executed according to the clinical protocol, regulatory requirements (GCP, FDA ...
Sr. Clinical Research Associate
Oregon, IL · On-site +1
... remote). * Actively participate in site feasibility assessments and site selection processes. * Ensure study conduct is executed according to the clinical protocol, regulatory requirements (GCP, FDA ...
Sr. Clinical Research Associate
Oregon, IL · On-site +1
... remote). * Actively participate in site feasibility assessments and site selection processes. * Ensure study conduct is executed according to the clinical protocol, regulatory requirements (GCP, FDA ...
This is a remote position open to applicants authorized to work for any employer within the United ... HIPPA and relevant FDA laws and regulations (certify completion where required). Basic ...
This is a remote position open to applicants authorized to work for any employer within the United ... HIPPA and relevant FDA laws and regulations (certify completion where required). Basic ...
This is a remote position open to applicants authorized to work for any employer within the United ... HIPPA and relevant FDA laws and regulations (certify completion where required). Basic ...
Quick apply
This is a remote position open to applicants authorized to work for any employer within the United ... HIPPA and relevant FDA laws and regulations (certify completion where required). Basic ...
Pharmaceutical Contracts Lawyers
Chicago, IL · On-site +1
$309K/yr
United States (remote or flexible on-site/hybrid depending on engagement) We are seeking ... Familiarity with regulatory considerations impacting pharma contracts (e.g., FDA, GMP, GxP ...
Pharmaceutical Contracts Lawyers
Chicago, IL · On-site +1
$309K/yr
United States (remote or flexible on-site/hybrid depending on engagement) We are seeking ... Familiarity with regulatory considerations impacting pharma contracts (e.g., FDA, GMP, GxP ...
Associate Territory Manager - Springfield, IL
Springfield, IL · Remote
$60K - $75K/yr
We are revolutionizing the sleep industry with our FDA-approved medical device, designed to reduce ... Ability to travel within defined geographic area. #LI-Remote The salary for this position will be ...
Quick apply
Associate Territory Manager - Springfield, IL
Springfield, IL · Remote
$60K - $75K/yr
We are revolutionizing the sleep industry with our FDA-approved medical device, designed to reduce ... Ability to travel within defined geographic area. #LI-Remote The salary for this position will be ...
TherOx SSO2 Therapy is the first FDA-approved therapy since the stent 20+ years ago to reduce ... For fully remote positions, compensation will comply with all applicable federal, state, and local ...
TherOx SSO2 Therapy is the first FDA-approved therapy since the stent 20+ years ago to reduce ... For fully remote positions, compensation will comply with all applicable federal, state, and local ...
Director, (GCP) Quality Assurance
Chicago, IL · On-site +1
Open to Hybrid in Chicago or Remote candidates Key Responsibilities & Core Ownership Champion ... FDA and ICH. * Oversee GCP framework for sponsored clinical trials to ensure required quality ...
Director, (GCP) Quality Assurance
Chicago, IL · On-site +1
Open to Hybrid in Chicago or Remote candidates Key Responsibilities & Core Ownership Champion ... FDA and ICH. * Oversee GCP framework for sponsored clinical trials to ensure required quality ...
Our core product is the WatchPAT ® ️ family, a revolutionary FDA-cleared portable home sleep ... For fully remote positions, compensation will comply with all applicable federal, state, and local ...
Our core product is the WatchPAT ® ️ family, a revolutionary FDA-cleared portable home sleep ... For fully remote positions, compensation will comply with all applicable federal, state, and local ...
Remote Fda information
See Illinois salary details
$22.8K - $34.7K
12% of jobs
$44.1K is the 25th percentile. Wages below this are outliers.
$34.7K - $46.5K
17% of jobs
$46.5K - $58.4K
14% of jobs
The median wage is $66.4K / yr.
$58.4K - $70.2K
12% of jobs
$70.2K - $82K
12% of jobs
$93K is the 75th percentile. Wages above this are outliers.
$82K - $93.9K
11% of jobs
$93.9K - $105.7K
7% of jobs
$105.7K - $117.6K
6% of jobs
$117.6K - $129.4K
4% of jobs
$129.4K - $141.3K
4% of jobs
$141.3K - $153.1K
2% of jobs
$22.8K
$77.8K
$153.1K
How much do remote fda jobs pay per year?
What is a remote FDA?
A Remote FDA job typically involves working for or with the U.S. Food and Drug Administration (FDA) from a remote location. These roles can include regulatory affairs, compliance, medical writing, research, and reviewing submissions for drug and medical device approvals. Remote FDA jobs require knowledge of FDA regulations, strong analytical skills, and experience in healthcare, pharmaceuticals, or related fields. They offer flexibility while maintaining high regulatory standards and ensuring public health and safety.
What are the typical daily responsibilities of a remote FDA compliance specialist?
A Remote FDA Compliance Specialist generally reviews and updates regulatory documents, conducts virtual audits, and monitors company practices for FDA compliance. They regularly collaborate with cross-functional teams, such as quality assurance, legal, and product development, to provide guidance on regulatory requirements and respond to compliance queries. Additionally, they prepare and submit necessary reports, maintain records for inspections, and stay current on evolving regulations. This remote structure allows flexibility but also demands excellent organization, communication, and self-discipline to ensure all deadlines and compliance standards are met.
What are the key skills and qualifications needed to thrive in the remote FDA position, and why are they important?
To excel as a Remote FDA Compliance Specialist, you need in-depth knowledge of FDA regulations, quality assurance procedures, and a background in life sciences or a related field. Proficiency in using compliance management systems, electronic document management tools, and relevant certifications such as RAC (Regulatory Affairs Certification) are often required. Exceptional attention to detail, self-motivation, and strong written and verbal communication skills are vital for remote collaboration and thorough documentation. These abilities ensure regulatory adherence, minimize compliance risks, and facilitate effective remote teamwork within the pharmaceutical or medical device industry.
What jobs can I do completely remotely as a remote FDA?
What are the most commonly searched types of Fda jobs in Illinois?
The most popular types of Fda jobs in Illinois are:
What are popular job titles related to Remote Fda jobs in Illinois?
For Remote Fda jobs in Illinois, the most frequently searched job titles are:
What job categories do people searching Remote Fda jobs in Illinois look for?
The top searched job categories for Remote Fda jobs in Illinois are:
What cities in Illinois are hiring for Remote Fda jobs?
Cities in Illinois with the most Remote Fda job openings:

Full-time
Re-posted 12 days ago
IQVIA rating
8.1
Based on 53 frontline employees who took The Breakroom Quiz
62nd of 226 rated it services
Job description
TheSolutionImplementation Leadis theendtoendexecution owner andsubjectmatterexpert for the development, validation, and operationalization of new connected medical device and digital health solutions.
This role partners closely with the Strategic Solutions Lead to evaluate, shape, and deliver new solution offerings aligned to the strategic priorities of the Connected Devices business, with a primary focus on the respiratoryserviceline. The role bridges strategy, execution, validation, and operational readiness, ensuring solutions progress from concept through BusinessGoLiveand are ready for scalable study deployment.
Key Responsibilitiesand Oversight
Experience supporting respiratory clinical trials (e.g., asthma, COPD, pulmonary indications) is required. Candidates without direct respiratory trial experience clearly demonstrated within their resume will not be considered.Solution Evaluation&Strategy Support
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Partner with Strategic Solutions Leads(SSL)to evaluate new digital health and medical device solutions alignedtoConnected Devices strategy.
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Provide SME input into solution feasibility, operational workflows, regulatory considerations, and validation approach.
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Support Strategic Solutions as needed withbusiness case development, budgetinputs,go-to-marketstrategyandcustomer-facingSME incustomer presentations.
EndtoEndSolution Startup Execution Ownership
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Ownendtoendexecution of approved solutions from business case approval through BusinessGoLive, serving as the single point of accountability for startup outcomes.
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Develop and manage the startup plan, including milestones, dependencies, risks, constraints, and mitigation strategies.
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Ensure solution design, operational workflows, and validation activities are aligned with study, program, and stakeholder needs.
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Confirmreadinessat eachstartupstageandbeforeBusiness GoLive.
CrossFunctionalOrchestration & Technical Leadership
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Lead and coordinate execution across Engineering, IT,Validation,QA, Regulatory, Data Management, Operations, Logistics, Vendors,Field Supportand Training.
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Translatehighlevelsolution concepts into clear device, system, service, and validation requirements understood by technical and validation teams.
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Support vendor relationships, including issue resolution, design alignment, and budget collaboration.
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Provideexpert troubleshooting guidance to operations and support teams; engage with sites and customers as needed to resolve complex issues.
SolutionLevelReadiness, Quality & Compliance
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Ensuresolutionlevelreadiness, including documentation, validation completion, training delivery, support models, and escalation pathways.
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Partner closely withSolution Specialiststo ensure regulatory and compliance requirements are met withoutlatestagedisruption.
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Leadquality management, process improvement, and continuous improvement initiatives.
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Contribute to internal SOPs, study templates, and site/patientfacingmaterials as a solution SME.
Governance, Escalation & Stakeholder ManagementOversight
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Own resolution ofstartuplevelissues; escalate appropriately when:
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Scope or solution intent isimpacted(to Strategic Solutions Lead)
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Timeline, investment, or delivery risk requires acceptance (to Governance / Sponsor)
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Provide clear, consistent communications to internal stakeholders, sponsors, and leadership on startup status, risks, and readiness.
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Transfer ownership at BusinessGoLiveto study execution leadership (e.g., CD Project Manager) andretainan escalation/support role forsolutionlevelissuesposthandoff.
Required Knowledge, Skills & Abilities
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Strong knowledge of digital health, connected medical devices, and regulated clinical environments is required and must be clearly outlined in your resume/CV.
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Working knowledge of FDA guidelines and global regulatory expectations and their operational impact.
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Advanced project and program management skills in complex, matrixed organizations.
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Excellent technical aptitude related to systems, platforms, integrations, and device workflows.
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Strong communication, stakeholder management, andexecutivelevelpresentation skills.
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Proven ability toestablishand maintain effective working relationships with internal teams, vendors, sponsors, sites, and clients.
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Occasional travel may berequired.
Minimum Education & Experience
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Bachelor's degree or equivalent combination of education, training, and experience.
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10+ years of relevant experience in healthcare, pharmaceutical, life sciences, or digital health environments.
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Demonstrated leadership experience managing people, operations, andcrossfunctionalinitiatives.
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Strong business acumen with experience supporting solution development, commercialization, and delivery.
This is a remote opportunity open to candidates currently residing in the United States.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $88,600.00 - $246,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.About IQVIA
Sourced by ZipRecruiter
At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Durham, NC, US