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Remote Biotech Nursing Jobs in California (NOW HIRING)

IQVIA

Clinical Trial Psych Rater

Carlsbad, CA · Remote

$62K - $156K/yr

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ...

Danaher

Sales Representative - Los Angeles

Los Angeles, CA · On-site +1

$188K - $198K/yr

... and biotechnology? At Radiometer, one of Danaher's 15+ operating companies, our work saves lives ... This position is part of the Blood Gas Sales Team and will be remote, travelling a territory ...

CareDx, Inc.

Clinical Trial Manager

Brisbane, CA · Remote

Bachelor's degree in life sciences, health sciences or equivalent degree/experience; RN or ... site/remote clinical monitoring experience in the biotechnology/pharmaceutical/CRO industry.

Merck & Co.

This remote position will be based in CA covering the West Region (CA, OR, WA, UT, NV, AZ, CO, HI ... A minimum of 3 years prior experience in the biotech/pharmaceutical or healthcare environment.A ...

Merck & Co.

This remote position will be based in CA covering the West Region (CA, OR, WA, UT, NV, AZ, CO, HI ... A minimum of 3 years prior experience in the biotech/pharmaceutical or healthcare environment.A ...

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All JobsBiotech Nursing JobsRemote Biotech Nursing JobsRemote Biotech Nursing Jobs in California

Remote Biotech Nursing information

See California salary details

$38.5K

$89.7K

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How much do remote biotech nursing jobs pay per year?

As of Aug 23, 2026, the average yearly pay for remote biotech nursing in California is $89,744.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,500.00 and $102,100.00 per year, depending on experience, location, and employer.

What is remote biotech nursing?

A Remote Biotech Nursing job involves providing patient support, education, and clinical guidance for biotech or pharmaceutical companies from a remote setting. Nurses in this role may assist with medication administration training, monitor patient outcomes, or collaborate with healthcare teams to ensure adherence to treatment plans. They often work with specialty medications, clinical trials, or patient assistance programs. Strong communication skills, technological proficiency, and a background in patient care are essential.

What does a remote biotech nurse do?

Remote Biotech Nursing professionals often monitor patient progress on advanced therapies, conduct virtual consultations, assist in clinical trials, and provide education on biotech treatments or devices. You may be responsible for documenting data in electronic health records, coordinating care with multidisciplinary teams, and troubleshooting patient issues related to biotechnology products. These roles usually require a mix of independent problem solving and regular collaboration with researchers, physicians, and biotech company representatives. Daily tasks are structured to ensure both high standards of patient care and adherence to regulatory guidelines in a remote setting.

What skills and qualifications are needed for remote biotech nursing?

Excelling in Remote Biotech Nursing requires an active RN license, a strong background in both clinical nursing and biotechnology concepts, and proficiency in telehealth practices. Familiarity with telemedicine platforms, electronic health records (EHR) systems, and specialized biotech software or equipment is highly valued. Effective communication, attention to detail, and the ability to work independently are vital soft skills that set top candidates apart. These capabilities ensure high-quality patient care, regulatory compliance, and effective collaboration in a virtual, technology-driven healthcare environment.

Do biotech companies hire remote biotech nurses?

Remote biotech nursing positions are available, especially in roles involving telehealth, patient education, and clinical support. Many biotech companies offer remote work options to accommodate flexible schedules and leverage digital communication tools, though some roles may require on-site presence for laboratory or clinical activities.

What are the most commonly searched types of Biotech Nursing jobs in California?

The most popular types of Biotech Nursing jobs in California are:

What are popular job titles related to Remote Biotech Nursing jobs in California?

For Remote Biotech Nursing jobs in California, the most frequently searched job titles are:

What job categories do people searching Remote Biotech Nursing jobs in California look for?

The top searched job categories for Remote Biotech Nursing jobs in California are:

What cities in California are hiring for Remote Biotech Nursing jobs?

Cities in California with the most Remote Biotech Nursing job openings:

Remote Biotech Nursing jobs near you
Infographic showing various Remote Biotech Nursing job openings in California as of August 2026, with employment types broken down into 86% Full Time, and 14% Part Time. Highlights an 100% Remote job distribution, with an average salary of $89,744 per year, or $43.1 per hour.

Manager, Pharmacovigilance Operations

Allogene Therapeutics

South San Francisco, CA • On-site, Remote

$140K - $150K/yr

Full-time

Medical

Re-posted yesterday

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 Manager, Pharmacovigilance Operations to join our team. You will provide support to the Allogene Pharmacovigilance department for drug safety operations including safety vendor oversight and management, serious adverse event reporting, support of study teams and projects, oversight of global safety database activities, and collaboration to support risk management and pharmacovigilance for all Allogene Therapeutics Clinical Trials and post marketing (where applicable). You will be interfacing cross-functionally at many levels in the organization as well as with our external vendors. You will be self-motivated, have strong communication and teamwork skills along with a robust ability to work independently, problem solve, manage work priorities, build collaborative relationships, and remain flexible to the needs of the teams and projects. This position will report to the Director, Pharmacovigilance. This role can be remote with frequent to travel to Allogene's South San Francisco headquarters or can be based out of our headquarters in South San Francisco, CA hybrid onsite 3 days a week.
Responsibilities include, but are not limited to:
  • Assist in Safety Vendor Oversight activities including tracking of KPIs, compliance metrics, and open query metrics.
  • Participate in eTMF filing for Allogene studies per TMF plans and procedures.
  • Schedule meetings and manage meeting agenda for PV team. Support Study Management Team meetings as needed.
  • Facilitate the preparation, completion, and submission of periodic safety reports (DSUR, 6M LL, etc.) and other regulatory filing documents.
  • Assist in MedDRA and WHODrug coding as needed.
  • Collaborate with the preparation and updates to safety section in the Investigator Brochures, RSI, DSURs, Protocols, ICFs, etc.
  • Manage Regulatory Reporting Requirements across all studies, ensure all requirements are met by the most current regulations.
  • Support projects or other initiatives from cross functional groups and departments
  • Support SPEED access requests and maintain the tracker, resolve access issues as applicable, perform monthly reconciliation.
  • Support SAE reconciliation between Clinical and Safety databases as needed.
  • Manage safety mailbox and provide responses to relevant communications.
  • Maintain internal and external distributions lists including providing updates and communications as appropriate.
  • Assist in the development and approval of PV SOPs and Work instructions
  • Initiate SMP review per schedule
  • Liaise with QA for CAPA activities in relation to, but not limited to, late SUSAR or aggregate report submissions as well as deviations relating to case management processes as defined per the SMPs or SOPs
  • Maintain SUSAR tracker in real time, perform monthly reconciliation and identify/resolve issues in timely manner.
  • Participate in regulatory inspections and PV audits to ensure quality, integrity and compliance with pharmacovigilance and safety reporting requirements
  • Other duties and projects as assigned

Position Requirements & Experience:
  • Bachelor's degree in life sciences, healthcare, or a related discipline; advanced degree (e.g., RN, BSN, PharmD) preferred
  • Minimum of 5 years of pharmacovigilance experience in a pharmaceutical or biotechnology company
  • Solid understanding and working knowledge of US and ex-US pharmacovigilance regulatory requirements (e.g., US Code of Federal regulations; European Union GVP legislation; and ICH Guidelines)
  • Proficiency in safety databases and other systems (e.g., Oracle Argus, ARISg, MedDRA, WHODrug, SPEED)
  • Excellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelines
  • Ability to work independently and collaboratively in a fast-paced environment and manage multiple projects simultaneously.
  • Experience with device safety reporting, eTMF filing, and regulatory inspections is a plus.
  • Strong interpersonal skills including verbal and written communication are essential in this collaborative work environment
  • Candidates must be authorized to work in the U.S.

We offer a chance to work with talented people in a collaborative environment and provide a top-notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company-wide shutdowns) and much more. The expected salary range for this role is $140,000 to $150,000 per year. 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, designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.

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