In support of FDA approved products, work within the Medical Science Liaison team's objectives ... LI-Remote Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all ...
In support of FDA approved products, work within the Medical Science Liaison team's objectives ... LI-Remote Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all ...
Ensure study conduct remains compliant with SOPs, GCP, FDA regulations, quality system requirements ... Location and Compensation This is a remote position supporting clinical sites throughout the United ...
Ensure study conduct remains compliant with SOPs, GCP, FDA regulations, quality system requirements ... Location and Compensation This is a remote position supporting clinical sites throughout the United ...
Senior Manager, Medical Writing
San Diego, CA ยท On-site +1
San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... Ensure adherence to applicable FDA, EMA, ICH, and other relevant regulatory guidelines and industry ...
Senior Manager, Medical Writing
San Diego, CA ยท On-site +1
San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... Ensure adherence to applicable FDA, EMA, ICH, and other relevant regulatory guidelines and industry ...
Director, Regulatory Affairs Strategy
San Diego, CA ยท On-site +1
$159K - $210K/yr
San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... Demonstrated success managing interactions with FDA and other major global health authorities
Director, Regulatory Affairs Strategy
San Diego, CA ยท On-site +1
$159K - $210K/yr
San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... Demonstrated success managing interactions with FDA and other major global health authorities
Engineer - Degreed II
Los Angeles, CA ยท On-site +1
$25 - $30/hr
LOS ANGELES, CA (Remote) Duration: 12 Months Remote Duties: * Primary responsibility is to perform ... Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies ...
Engineer - Degreed II
Los Angeles, CA ยท On-site +1
$25 - $30/hr
LOS ANGELES, CA (Remote) Duration: 12 Months Remote Duties: * Primary responsibility is to perform ... Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies ...
Provide technical troubleshooting for remote monitoring issues and workflow challenges, escalating ... Adhere to all FDA, regulatory, and company quality requirements. * Maintain accurate documentation ...
Quick apply
Provide technical troubleshooting for remote monitoring issues and workflow challenges, escalating ... Adhere to all FDA, regulatory, and company quality requirements. * Maintain accurate documentation ...
... FDA promotional guidelines, regulations, and ethical guidelines is preferred. * Demonstrated ... Remote
... FDA promotional guidelines, regulations, and ethical guidelines is preferred. * Demonstrated ... Remote
Patient Operations Management Associate (Contract)
South San Francisco, CA ยท On-site +1
$50 - $60/hr
Understands basic FDA & EMA regulations, ICH guidelines, GCP, and GMP. * Experience with clinical ... REMOTE
Patient Operations Management Associate (Contract)
South San Francisco, CA ยท On-site +1
$50 - $60/hr
Understands basic FDA & EMA regulations, ICH guidelines, GCP, and GMP. * Experience with clinical ... REMOTE
Regional Business Director, TTR - Northern California
San Francisco, CA ยท On-site +1
$204K - $276K/yr
Food and Drug Administration (FDA) recently approved the supplemental New Drug Application (sNDA ... Demonstrated commitment to ethics and integrity. #LI-ST1 #LI-Remote U.S. Pay Range $204,000.00 ...
Regional Business Director, TTR - Northern California
San Francisco, CA ยท On-site +1
$204K - $276K/yr
Food and Drug Administration (FDA) recently approved the supplemental New Drug Application (sNDA ... Demonstrated commitment to ethics and integrity. #LI-ST1 #LI-Remote U.S. Pay Range $204,000.00 ...
Senior Director, Clinical Operations
San Diego, CA ยท On-site +1
$245K - $260K/yr
Strong knowledge of ICH GCP, FDA regulations, and global clinical regulatory guidelines. * Strong ... Remote permitted upon approval, with ability to travel up to 25% for meetings or site visits as ...
Senior Director, Clinical Operations
San Diego, CA ยท On-site +1
$245K - $260K/yr
Strong knowledge of ICH GCP, FDA regulations, and global clinical regulatory guidelines. * Strong ... Remote permitted upon approval, with ability to travel up to 25% for meetings or site visits as ...
Associate Director, Clinical Trial Management
San Francisco, CA ยท On-site +1
$179K - $200K/yr
Remains current with therapeutic areas under study, industry practices / trends and FDA ... Benefits: * A stimulating and rewarding workplace includes flexible work schedules, remote ...
Associate Director, Clinical Trial Management
San Francisco, CA ยท On-site +1
$179K - $200K/yr
Remains current with therapeutic areas under study, industry practices / trends and FDA ... Benefits: * A stimulating and rewarding workplace includes flexible work schedules, remote ...
Sr. Clinical Research Associate (Field)
Los Gatos, CA ยท Remote
$120K - $140K/yr
This is a full time, remote position with anticipated travel of up to 80%. Preferred geographic ... Strong working knowledge of GCP, ISO 14155 and FDA guidelines. * Proficient in EDC, eTMF, and ...
Sr. Clinical Research Associate (Field)
Los Gatos, CA ยท Remote
$120K - $140K/yr
This is a full time, remote position with anticipated travel of up to 80%. Preferred geographic ... Strong working knowledge of GCP, ISO 14155 and FDA guidelines. * Proficient in EDC, eTMF, and ...
Sr. Regulatory Compliance Specialist
Irvine, CA ยท On-site +1
Remote Position Summary: The Senior Regulatory Compliance Specialist is responsible for supporting ... food labeling under FDA and USDA jurisdictions * A working knowledge of Kosher and Halal ...
Sr. Regulatory Compliance Specialist
Irvine, CA ยท On-site +1
Remote Position Summary: The Senior Regulatory Compliance Specialist is responsible for supporting ... food labeling under FDA and USDA jurisdictions * A working knowledge of Kosher and Halal ...
Medical Science Liaison, Sleep - CA, HI
Los Angeles, CA ยท On-site +1
In support of FDA approved products, work within the Medical Science Liaison team's objectives ... LI-Remote Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all ...
Medical Science Liaison, Sleep - CA, HI
Los Angeles, CA ยท On-site +1
In support of FDA approved products, work within the Medical Science Liaison team's objectives ... LI-Remote Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all ...
Clinical Applications Specialist
Aliso Viejo, CA ยท On-site +1
S. based, remote position that requires regular travel to clinical trial sites across the country ... Maintain compliance with FDA regulations, GCP guidelines, and SpyGlass Pharma's internal SOPs.
Clinical Applications Specialist
Aliso Viejo, CA ยท On-site +1
S. based, remote position that requires regular travel to clinical trial sites across the country ... Maintain compliance with FDA regulations, GCP guidelines, and SpyGlass Pharma's internal SOPs.
Corporate Counsel, Global Legal Technical Operations & Facilities
South San Francisco, CA ยท On-site +1
$181K - $337K/yr
... on FDA/cGMP related matters. Location * This role is located at Genentech's South San Francisco, California campus. A remote working arrangement is not available. * Relocation benefits are not ...
Corporate Counsel, Global Legal Technical Operations & Facilities
South San Francisco, CA ยท On-site +1
$181K - $337K/yr
... on FDA/cGMP related matters. Location * This role is located at Genentech's South San Francisco, California campus. A remote working arrangement is not available. * Relocation benefits are not ...
Director / Senior Director of Regulatory Operations
San Diego, CA ยท On-site +1
$268K/yr
This role can be on-site or remote. Duties/Responsibilities: * Build, lead, and scale Regulatory ... Experience supporting programs utilizing FDA Accelerated Approval, Breakthrough Therapy Designation ...
Director / Senior Director of Regulatory Operations
San Diego, CA ยท On-site +1
$268K/yr
This role can be on-site or remote. Duties/Responsibilities: * Build, lead, and scale Regulatory ... Experience supporting programs utilizing FDA Accelerated Approval, Breakthrough Therapy Designation ...
Sr. Regulatory Compliance Specialist
Irvine, CA ยท On-site +1
Remote Position Summary: The Senior Regulatory Compliance Specialist is responsible for supporting ... food labeling under FDA and USDA jurisdictions * A working knowledge of Kosher and Halal ...
Sr. Regulatory Compliance Specialist
Irvine, CA ยท On-site +1
Remote Position Summary: The Senior Regulatory Compliance Specialist is responsible for supporting ... food labeling under FDA and USDA jurisdictions * A working knowledge of Kosher and Halal ...
Director / Senior Director of Regulatory Operations
San Diego, CA ยท On-site +1
$159K - $209K/yr
This role can be on-site or remote. Duties/Responsibilities: * Build, lead, and scale Regulatory ... Experience supporting programs utilizing FDA Accelerated Approval, Breakthrough Therapy Designation ...
Director / Senior Director of Regulatory Operations
San Diego, CA ยท On-site +1
$159K - $209K/yr
This role can be on-site or remote. Duties/Responsibilities: * Build, lead, and scale Regulatory ... Experience supporting programs utilizing FDA Accelerated Approval, Breakthrough Therapy Designation ...
Manager, Regulatory Affairs
San Francisco, CA ยท On-site +1
$127K - $165K/yr
Lead FDA submissions (510(k) or pre-submissions) with the team, including wearable devices, as well ... Remote - US Actual compensation may vary depending on job-related factors including knowledge ...
Manager, Regulatory Affairs
San Francisco, CA ยท On-site +1
$127K - $165K/yr
Lead FDA submissions (510(k) or pre-submissions) with the team, including wearable devices, as well ... Remote - US Actual compensation may vary depending on job-related factors including knowledge ...
Remote Fda information
See California salary details
$25.5K - $38.7K
12% of jobs
$49.2K is the 25th percentile. Wages below this are outliers.
$38.7K - $51.9K
17% of jobs
$51.9K - $65.1K
14% of jobs
The median wage is $74.1K / yr.
$65.1K - $78.3K
12% of jobs
$78.3K - $91.6K
12% of jobs
$103.8K is the 75th percentile. Wages above this are outliers.
$91.6K - $104.8K
11% of jobs
$104.8K - $118K
7% of jobs
$118K - $131.2K
6% of jobs
$131.2K - $144.4K
4% of jobs
$144.4K - $157.7K
4% of jobs
$157.7K - $170.9K
2% of jobs
$25.5K
$86.8K
$170.9K
How much do remote fda jobs pay per year?
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 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 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 are the most commonly searched types of Fda jobs in California?
The most popular types of Fda jobs in California are:
What are popular job titles related to Remote Fda jobs in California?
For Remote Fda jobs in California, the most frequently searched job titles are:
What job categories do people searching Remote Fda jobs in California look for?
The top searched job categories for Remote Fda jobs in California are:
What cities in California are hiring for Remote Fda jobs?
Cities in California with the most Remote Fda job openings:

Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 8 days ago
Job description
If you are a current Jazz employee please apply via the Internal Career site
Jazz Pharmaceuticalsis a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered inDublin, Irelandwith research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visitwww.jazzpharmaceuticals.comfor more information.
Job DescriptionThe Medical Science Liaison (MSL) position serves as the primary field-based scientific expert for Jazz Pharmaceuticals' products. The MSL will establish and maintain scientific and clinical relationships with medical professionals, researchers, and other members of the scientific community in the therapeutic area of Sleep Medicine/Neuroscience. MSLs will also mentor and manage group and individual projects. In conjunction with the National Director, Medical Science Liaisons, Associate Director, Medical Science Liaisons, and Regional Medical Directors, the Medical Science Liaison team will integrate their scientific expertise and knowledge in all interactions and ensure compliant and successful scientific communication and education in disease states of interest to Jazz Pharmaceuticals.
This is afield-based position coveringCalifornia and Hawaii requires professionals with established personal and scientific credibility to interact with thought leaders and academic centers of excellence.
Essential Functions/Responsibilities
Provide field-based scientific exchange and communication of FDA approved and pipeline products
In support of FDA approved products, work within the Medical Science Liaison team's objectives
Identify, establish, and maintain scientific relationships with opinion leaders regarding disease-state and product-specific information
Facilitate scientific development of pipeline compounds at research centers, and secure the company's presence in the designated therapeutic areas
Support the clinical operations organization, as needed, in Jazz Pharmaceuticals sponsored research
Serve as primary liaison with investigators interested in developing and performing investigator initiated research
Cross-functional nature of role requires close alignment with the Medical Affairs, Commercial, and Clinical Development groups
Document and forward reports of adverse events according to Jazz's policy to ensure safe and effective use of Jazz Pharmaceuticals' products
Attend and provide scientific support of Medical Affairs activities and scientific sessions at regional and national congress meetings
Develop and prioritize solutions to problems, understand relationship between actions and results and able to understand and appreciate needs of customers
Proactively seeks out and demonstrates successful peer coaching of other team members
Successfully manages at least two large cross-functional projects with demonstrated leadership and collaboration skills while successfully maintaining geographical responsibilities
Required Knowledge, Skills, and Abilities
Ability to effectively communicate scientific data to both internal and external customers, including opinion leaders and managed care organizations
Knowledge of geography and key opinion leaders preferred
Thorough understanding of applicable federal and state regulatory requirements for field-based scientific personnel
Demonstrated ability to develop trust and relationships with opinion leaders in disease states of interest
Collaborative, team-based approach; ability to network and partner with internal and external stakeholders, including commercial and R&D partners, medical opinion leaders, academic institutions, large group practices, managed care organizations, medical directors and pharmacy directors in institutional practices
Ability to work evenings and weekends
Ability and willingness to travel 60% of work days
Valid driver's license and live within 60 miles of a major airport
Required/Preferred Education and Licenses
An advanced doctorate degree (PharmD, MD, DO, PhD or equivalent)
A minimum of 0-2 years of experience in the pharmaceutical industry and/or clinical/research experience (MSL experience preferred)
Preference will be given those with experience in Sleep Medicine; however, experience in Neurology, Psychiatry or other relevant backgrounds will be considered
#LI-Remote
Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.
FOR US BASED CANDIDATES ONLY
Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive.For this role, the full and complete base pay range is:
$160,000.00 - $240,000.00Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis.
At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.
The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation.For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html