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Nurses Biotech Jobs in Massachusetts (NOW HIRING)

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related healthcare field. Prior experience in clinical research or clinical trial coordination is preferred.

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related healthcare field. Prior experience in clinical research or clinical trial coordination is preferred.

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related healthcare field. Prior experience in clinical research or clinical trial coordination is preferred.

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related healthcare field. Prior experience in clinical research or clinical trial coordination is preferred.

Clinovo

Clinical Trial Manager

Cambridge, MA · On-site

$175K/yr

Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline; advanced degree preferred. * Minimum of 5 years of clinical operations experience within the biotechnology ...

NewYork-Presbyterian

CRNA

Haverhill, MA · On-site

$205/hr

CRNAs Certified Registered Nurse Anesthetist - CRNA - Per Diem-NYP/Brooklyn Methodist Hospital ... NYP will not reimburse for travel expenses. _____ * 2026 Best Companies in Healthcare, Biotech ...

NewYork-Presbyterian

CRNA

Fall River, MA · On-site

$205/hr

CRNAs Certified Registered Nurse Anesthetist - CRNA - Per Diem-NYP/Brooklyn Methodist Hospital ... NYP will not reimburse for travel expenses. _____ * 2026 Best Companies in Healthcare, Biotech ...

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Nurses Biotech information

What is a nurse in biotech?

Nurses in biotech are registered nurses who work within the biotechnology industry, often collaborating with scientists, researchers, and medical professionals to develop and implement new medical technologies, devices, or pharmaceuticals. They may be involved in clinical trials, patient education, regulatory compliance, or product development. These nurses use their clinical expertise to ensure that biotechnological advancements are safe, effective, and meet patient care standards. Their role bridges the gap between clinical practice and scientific innovation, making them valuable assets in the advancement of healthcare.

What skills and qualifications are needed to thrive as a nurse in the biotech industry?

To thrive as a Nurse in the Biotech industry, you need a solid nursing background with clinical expertise, a nursing degree, and active RN licensure, often complemented by knowledge of biotechnology applications. Familiarity with laboratory information management systems (LIMS), clinical trial protocols, and compliance certifications like GCP are typically required. Strong communication, attention to detail, and adaptability help nurses collaborate with interdisciplinary teams and navigate evolving biotech environments. These skills and qualifications are crucial for ensuring patient safety, supporting research integrity, and bridging clinical practice with innovative biotech solutions.

How do nurses in the biotech industry typically collaborate with research and development teams?

Nurses in the biotech sector often work closely with research and development teams to provide clinical insights, ensure patient safety, and contribute to the design and execution of clinical trials. Their healthcare expertise allows them to bridge the gap between laboratory research and patient care, ensuring that protocols are practical and ethical. Effective collaboration usually involves regular meetings, sharing feedback on study protocols, and assisting with data collection from a clinical perspective. This cross-functional teamwork is essential for translating innovative biotech solutions into real-world healthcare improvements.

What is the difference between Nurses Biotech vs Clinical Research Nurses?

AspectNurses BiotechClinical Research Nurses
CredentialsRN license, possibly biotech-specific certificationsRN license, clinical research certifications often preferred
Work EnvironmentBiotech labs, pharmaceutical companies, research facilitiesHospitals, research clinics, clinical trial sites
Employer & IndustryBiotech firms, pharmaceutical companiesResearch institutions, hospitals, CROs
Job FocusSupporting biotech product development, lab proceduresManaging clinical trials, patient care in research

While both roles require RN licensure and involve research, Nurses Biotech primarily work in biotech labs supporting product development, whereas Clinical Research Nurses focus on managing clinical trials and patient care in clinical settings. The choice depends on whether you prefer lab-based biotech work or patient-centered clinical research.

How much do nurses biotech make?

Nurses working in biotech or pharmaceutical companies typically earn between $70,000 and $100,000 annually, depending on experience, location, and certifications. Roles may include clinical research nurses or biotech nurse specialists, often requiring specialized training and knowledge of laboratory or clinical environments.

What are popular job titles related to Nurses Biotech jobs in Massachusetts?

For Nurses Biotech jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Nurses Biotech jobs in Massachusetts look for?

The top searched job categories for Nurses Biotech jobs in Massachusetts are:

What cities in Massachusetts are hiring for Nurses Biotech jobs?

Cities in Massachusetts with the most Nurses Biotech job openings:

Nurses Biotech jobs near you
Infographic showing various Nurses Biotech job openings in Massachusetts as of August 2026, with employment types broken down into 2% As Needed, 62% Full Time, 16% Part Time, and 20% Contract. Highlights an 99% Physical, and 1% Remote job distribution.

Clinical Research Coordinator

Boston, MA • On-site

Winaxis
IT Services • 11 - 50 employees
Learn more about Winaxisexternal

$26.25 - $35/hr

Full-time

Re-posted 26 days ago

Job description

Job Summary: The Clinical Research Coordinator (CRC) is responsible for coordinating and managing clinical trials in accordance with study protocols, Good Clinical Practice (GCP) guidelines, institutional policies, and applicable regulatory requirements. The role involves participant recruitment, study documentation, data collection, and ensuring the smooth execution of research activities while safeguarding participant safety and data integrity. Key Responsibilities: Coordinate and oversee day-to-day activities related to assigned clinical studies. Review study protocols and ensure all trial activities are conducted in compliance with protocol requirements. Recruit, screen, and enroll eligible study participants according to inclusion and exclusion criteria. Obtain and document informed consent from study participants prior to study procedures. Schedule participant visits and coordinate study assessments, procedures, and follow-ups. Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study records. Monitor participant safety by identifying, documenting, and reporting adverse events and serious adverse events in accordance with regulatory timelines. Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs), laboratory personnel, and other study stakeholders. Prepare for and support sponsor monitoring visits, audits, and regulatory inspections. Ensure adherence to Good Clinical Practice (GCP), institutional policies, and applicable local and international regulations. Track study timelines, recruitment targets, and protocol milestones. Assist with study initiation, amendments, close-out activities, and archiving of study documents. Maintain confidentiality of participant information and research data at all times. Required Qualifications: Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related healthcare field. Prior experience in clinical research or clinical trial coordination is preferred. Certification in Good Clinical Practice (GCP) is an advantage. Required Skills: Strong understanding of clinical trial processes and research ethics. Knowledge of ICH-GCP guidelines and regulatory requirements. Excellent organizational and time-management skills. Strong verbal and written communication abilities. Attention to detail and accuracy in documentation. Proficiency in Microsoft Office applications and EDC systems. Ability to work independently and collaboratively within multidisciplinary teams. Effective problem-solving and interpersonal skills. Working Conditions: Work is typically performed in hospitals, research institutions, academic medical centers, or clinical research organizations. May require flexibility to accommodate participant schedules and sponsor visits.