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Remote Fda Internship Jobs in California (NOW HIRING)

Biointellisense

DevOps Engineer

Redwood City, CA · Remote

$140K - $170K/yr

Our FDA-cleared and award-winning BioButton wearables, BioHub gateways, BioMobile applications ... Northern California (local) / Remote All candidate must be located in the United States to be ...

All JobsFda JobsRemote Fda Internship JobsRemote Fda Internship Jobs in California

Remote Fda Internship information

What is a remote FDA internship?

A remote FDA internship is a temporary, educational position that allows students or recent graduates to work with the U.S. Food and Drug Administration (FDA) from a remote location, rather than on-site. Interns may assist with projects related to public health, regulatory affairs, research, policy analysis, or data management. These internships are designed to provide practical experience and exposure to the FDA’s role in protecting public health, while offering flexibility for those who cannot relocate or commute. Remote FDA internships may be paid or unpaid, and requirements vary depending on the specific program or department. Applicants typically need to be enrolled in an accredited college or university and meet other eligibility criteria.

What types of projects or responsibilities can I expect as a remote FDA intern?

As a remote FDA intern, you may be involved in a variety of projects such as assisting with research and data analysis, supporting regulatory review processes, preparing reports, or helping with public health initiatives. Your exact responsibilities will depend on your assigned department, but remote interns typically collaborate with mentors and team members through virtual meetings and online platforms. This role offers exposure to federal regulatory practices, and you’ll gain valuable experience in navigating structured government workflows. Effective communication and time management are key to succeeding in this remote setting.

What are the key skills and qualifications needed to thrive as a remote FDA intern?

To thrive as a Remote FDA Intern, you generally need a background in life sciences, public health, or a related field, often supported by current enrollment in a relevant degree program. Familiarity with regulatory databases, Microsoft Office Suite, and scientific literature review tools is commonly required. Strong written communication, attention to detail, and initiative are crucial soft skills for excelling in remote collaboration and research tasks. These skills ensure interns can contribute effectively to regulatory projects, maintain compliance standards, and support the FDA’s mission in a virtual environment.

What is the difference between Remote Fda Internship vs Remote Fda Associate?

AspectRemote Fda InternshipRemote Fda Associate
Required CredentialsTypically enrolled in or recent graduate of relevant health/science programsBachelor's or Master's in life sciences, with some experience preferred
Work EnvironmentInternship program, often part-time or seasonal, supervised by professionalsFull-time remote role, more independent with ongoing responsibilities
Employer & Industry UsageUsed by FDA and biotech companies for training and entry-level talentCommon in regulatory affairs teams within pharmaceutical and biotech firms

The Remote Fda Internship is an entry-level, temporary position designed for students or recent graduates gaining industry exposure. In contrast, the Remote Fda Associate is a more advanced, full-time role requiring some experience, focusing on regulatory tasks. Both roles are vital in the FDA and biotech sectors but differ in experience level, responsibilities, and duration.

What cities in California are hiring for Remote Fda Internship jobs?

Cities in California with the most Remote Fda Internship job openings:

Remote Fda Internship jobs near you
Infographic showing various Remote Fda Internship job openings in California as of August 2026, with employment types broken down into 6% Internship, 65% Full Time, 26% Part Time, and 3% Contract. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution.

Patient Operations Management Associate (Contract)

Allogene Therapeutics

South San Francisco, CA • On-site, Remote

$50 - $60/hr

Contractor

Posted 17 days ago

Job description

Job Description
About Allogene:
Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of "off-the-shelf" CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients.
About the role:
We are seeking a highly motivated individual to join us as a Patient Operations Management Associate in our Clinical Operations team. The Patient Operations Management Associate role is responsible for supporting the oversight and management of the Participant Pathway related to the scheduling, coordination and tracking of investigational product through the allogeneic enrollment process. This role will help oversee aspects of clinical logistics for one or more clinical trials at Allogene. The role must be able to work collaboratively with cross-functional teams to support study enrollment and corporate initiatives. This is a 6-month contract opportunity.
Responsibilities include, but are not limited to:
  • Manage patient scheduling tools, guidelines, work instructions, and dashboards for cell therapy product delivery.
  • Support tracking and reporting investigational product logistics information and patient metrics utilizing databases, spreadsheets, and other tools.
  • Support communication plans and templates for regular updates with Clinical Operations and sites on patient status.
  • Support tracking and reporting investigational product logistics information and patient metrics utilizing databases, spreadsheets, and other tools.
  • Train to handling manuals and training materials for clinical sites regarding patient material shipping and product receipt to CRO staff, clinical site staff, and other audiences as needed.
  • Support IP logistics and supply chain processes for domestic and international clinical trial activities.
  • Support the management of vendors and systems associated with IP logistics with cross-functional stakeholder(s).
  • Participate in meetings to support the launch of clinical trials and ongoing enrollment activities.
  • Collaborate with key stakeholders to ensure a thorough patient journey program.
  • Recommend process improvements and promote a culture of collaboration and execution excellence.
  • Provides training to CRO staff, clinical site staff, and other audiences as needed
  • Participate in the development, review and implementation of SOPs and processes, as needed.
  • Other duties as assigned

Position Requirements & Experience:
  • Bachelor's degree or relevant experience
  • Preferred experience in healthcare industry and FDA regulated environment.
  • Understands basic FDA & EMA regulations, ICH guidelines, GCP, and GMP.
  • Experience with clinical logistics and pharmaceutical supply chain systems.
  • Experience managing logistics activities for outsourced drugs such as warehousing, transportation, customs clearance and invoicing.
  • Familiar with domestic and international logistics/transport of biologic material: IATA, ICAO, ADR, DOT, WHO.
  • Excellent interpersonal and collaboration skills.
  • Able to work independently and collaboratively to accomplish primary objectives.
  • Demonstrates strong analytical skills to develop solutions to a variety of complex problems.
  • Organizational skills with the ability to multi-task and prioritize planning of activities
  • Can support or lead vendor management efforts, as needed.
  • Self-starter, possessing a strong work ethic, ability to drive change, and passion for helping others.
  • Candidates must be authorized to work in the U.S.
  • East Coast-based candidates are preferred.
  • Willingness to eventually support EU operations.

We offer a chance to work with talented people in a collaborative environment. The expected salary range for this role is $50.00 to $60.00 per hour. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law.
As an equal opportunity employer, Allogene is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.
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