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Remote Biotech Nursing Jobs (NOW HIRING)

Perform clinical research site activities, which can include onsite or remote monitoring, co ... Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related field. * 5 to 8 ...

This is a permanent remote opportunity, with potential hybrid arrangement depending on location ... Nursing degree or relevant degree or background preferred. In some cases, an equivalency ...

Sr Medidata RAVE Programmer Remote from anywhere in the U.S. or Canada Contract/Corp to Corp JOB ... g., nursing certification, medical or laboratory technology) • 2-4years EDC Programming ...

This remote role requires twenty percent face-to-face interactions and can be based on the ... Nursing degree/healthcare clinical experience * Above-average skills with technology, including ...

This remote role requires twenty percent face-to-face interactions and can be based on the ... Nursing degree/healthcare clinical experience * Above-average skills with technology, including ...

This remote role requires twenty percent face-to-face interactions and can be based on the ... Nursing degree/healthcare clinical experience * Above-average skills with technology, including ...

Inspection Readiness Manager

OR · On-site +1

$114K - $143K/yr

It is key to our becoming one of the world's leading biotechnology companies. We are global ... Bachelor Degree in Life Sciences or RN or equivalent * 7 years work experience in life sciences or ...

... and biotechnology? At Radiometer, one of Danaher's 15+ operating companies, our work saves lives ... Respiratory therapy, nurse, clinical lab or similar work experience helpful. * An understanding of ...

... and biotechnology? At Radiometer, one of Danaher's 15+ operating companies, our work saves lives ... Respiratory therapy, nurse, clinical lab or similar work experience helpful. * An understanding of ...

... and biotechnology? At Radiometer, one of Danaher's 15+ operating companies, our work saves lives ... Respiratory therapy, nurse, clinical lab or similar work experience helpful. * An understanding of ...

... and biotechnology? At Radiometer, one of Danaher's 15+ operating companies, our work saves lives ... Respiratory therapy, nurse, clinical lab or similar work experience helpful. * An understanding of ...

... and biotechnology? At Radiometer, one of Danaher's 15+ operating companies, our work saves lives ... Respiratory therapy, nurse, clinical lab or similar work experience helpful. * An understanding of ...

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Remote Biotech Nursing information

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$39K

$90.9K

$144K

How much do remote biotech nursing jobs pay per year?

As of Jun 9, 2026, the average yearly pay for remote biotech nursing in the United States is $90,935.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $103,500.00 per year, depending on experience, location, and employer.

What are the typical daily responsibilities for someone in Remote Biotech Nursing?

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 is a Remote Biotech Nursing job?

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 are the key skills and qualifications needed to thrive in the Remote Biotech Nursing position, and why are they important?

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.

More about Remote Biotech Nursing jobs
What cities are hiring for Remote Biotech Nursing jobs? Cities with the most Remote Biotech Nursing job openings:
What are the most commonly searched types of Biotech Nursing jobs? The most popular types of Biotech Nursing jobs are:
What states have the most Remote Biotech Nursing jobs? States with the most job openings for Remote Biotech Nursing jobs include:
Infographic showing various Remote Biotech Nursing job openings in the United States as of May 2026, with employment types broken down into 90% Full Time, 5% Temporary, and 5% Contract. Highlights an 100% Remote job distribution, with an average salary of $90,935 per year, or $43.7 per hour.

Senior Clinical Trial Manager

ARTBIO

Cambridge, MA • On-site, Remote

Full-time

Posted 16 days ago


Job description

Summary The Senior Clinical Trial Manager will lead the day-to-day activities in a clinical trial, and support the program strategy in a highly collaborative environment. The successful candidate will manage members of the clinical operations team, including those at CROs and study vendors, work collaboratively with clinical trial sites, and partner with key internal stakeholders to ensure clinical trial deliverables are completed on time, within budget, and in line with regulatory requirements. The successful candidate must be comfortable working independently and cross-functionally to ensure study compliance and data quality.
Responsibilities
  • Lead cross-functional meetings with the Clinical Development, Clinical Operations, Data Management, regulatory, Quality, and Clinical Supply Chain.
  • Support the development within budget and on schedule.
  • Drive study startup activities, including feasibility, site selection, and timelines.
  • Manage activities of Phase 1 and 2 clinical trial investigators with a focus on the US to ensure compliance with the study protocol and overall clinical objectives.
  • Maintain clear communication across all departments.
  • Proactively manage, identify, and mitigate risks with the study team.
  • Serve as cross-functional lead for the clinical trial.
  • Identify and report potential program issues and implement CAPAs where necessary.
  • Act as the primary point of contact for trial execution and escalation.
  • Provide financial and management accountability updates to internal stakeholders as required.
  • Lead the oversight of CROs and vendors in partnership with the rest of the Clinical Operations team to assure the integrity of clinical data with respect to accuracy, accountability, and documentation through review of case report forms, source documents, medical records, etc.
  • Perform clinical research site activities, which can include onsite or remote monitoring, co-monitoring, and training visits.
  • Ensure that all study documentation and SOPS are maintained according to applicable regulations and industry-accepted standards, both in the field and in-house.
  • Contribute to the development of study documentation, including protocol review, study operations manuals, SOPs, ICFs, CRFs, CSRs, IBs, and data cleaning.
  • Collaborate with Clinical, Regulatory, and Quality team members to ensure compliance of department/study activities with FDA regulations, guidelines, and principles of ICH GCP and company SOPs.
  • Limited travel possible to clinical sites to supervise and/or monitor clinical studies (~25%).
Qualifications & Education
  • Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related field.
  • 5 to 8 years of experience in clinical operations or direct study management in a biotech or pharmaceutical company (Industry Sponsor).
  • Excellent communication skills.
  • Extensive experience managing US clinical sites, including start-up activities and monitoring.
  • Experience in oncology (preferably in solid tumors); radiopharmaceuticals a plus.
  • Experience overseeing CROs and vendors, maintaining timelines, and overseeing budgets.
  • Experience with clinical data review and data management processes.
  • Excellent communication, organizational, and leadership skills.
  • Ability to work independently, plan, prioritize, and risk mediate in a fast-paced environment.
  • Strong working knowledge of GCP, ICH, and FDA regulations.
About Us
Channeling Energy. Changing Lives. ARTBIO redefines cancer care by discovering and developing a new class of Alpha Radioligand Therapies (ARTs), powered by unique Pb-212 isotope technology and seamless supply. Our team works tirelessly to bring therapies that matter to patients who need them.
 
The unique ARTBIO approach selects the optimal alpha-precursor isotope (212Pb) and tumor-specific targets to create therapeutics with the potential for the highest efficacy and safety. The company's AlphaDirect technology, a first-of-its-kind 212Pb isolation method, enables a distributed manufacturing approach for the reliable production and delivery of ARTs. ARTBIO is advancing multiple pipeline programs, with lead program AB001 currently in first-in-human trials. The company is shaped by a long-standing scientific legacy with nearly a century of pioneering work in radiation therapy conducted at the University of Oslo and Norway's Radium Hospital.
 
Cancer is relentless. So are we. We are driven by a desire to do better for cancer patients, lowering the burden of toleration and safety while at the same time raising the bar on clinical efficacy and duration. As an emerging, global biotech with locations in Boston, Basel, London, and Oslo, we take advantage of diverse scientific depth and insights, which makes ARTBIO a unique place to work. 
 
 
EEO Statement
ARTBIO is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. If you have a disability or special need that requires accommodation, please let us know.
 
Questions and Application Process
If interested, please apply and send your CV to [email protected]. All inquiries are treated confidentially.
 
ARTBIO does not accept unsolicited resumes from external agencies or recruiters. Submission of a resume without a prior written agreement does not create any express or implied contract between ARTBIO and the agency. ARTBIO will not pay any fees related to unsolicited resumes.
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