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Biotech Associate Jobs in New York (NOW HIRING)

Legend Biotech US

Senior Clinical Trial Associate

Somerset, NJ · On-site

$35.50 - $48.25/hr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Legend Biotech is seeking a Senior Clinical Trial Associate as part of the Clinical Operations team ...

Legend Biotech US

Operations Associate

Raritan, NJ · On-site

Legend Biotech is seeking an Operations Associate as part of the Manufacturing & Supply team based in Raritan, NJ. Role Overview This position is responsible for performing manufacturing procedures ...

Legend Biotech

Research Associate II

Piscataway, NJ · On-site

At Legend Biotech, we are excited to bring clinical trials to patients in our pursuit of a cure. While we are focusing on CAR-T in multiple myeloma, we firmly believe the prospects of cellular ...

Legend Biotech

Research Associate II

Piscataway, NJ · On-site

At Legend Biotech, we are excited to bring clinical trials to patients in our pursuit of a cure. While we are focusing on CAR-T in multiple myeloma, we firmly believe the prospects of cellular ...

Astrix Inc

Assembly Associate (Biotech)

Somerset, NJ · On-site

$20 - $25/hr

They are looking for a skilled Assembly Associate to join their growing team in Somerset County, NJ! This is a great opportunity to contribute to an innovative life science organization! Pay rate ...

Astrix Inc.

Assembly Associate (Biotech)

Bridgewater, NJ · On-site

$57.31/hr

They are looking for a skilled Assembly Associate to join their growing team in Somerset County, NJ! This is a great opportunity to contribute to an innovative life science organization! Pay rate ...

Stifel

Research Associate II - Biotechnology

Manhattan, NY · On-site

$110K - $175K/yr

Conduct propriety research and due diligence on companies in the biotech sector, using internal and ... Associate I level * Minimum Required: SIE, FINRA Series 86, and 87 expected to be obtained upon ...

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Biotech Associate information

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How much do biotech associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for biotech associate in New York is $21.74, according to ZipRecruiter salary data. Most workers in this role earn between $16.30 and $22.60 per hour, depending on experience, location, and employer.

What is a biotech associate?

Biotech Associates are professionals who support scientific research, development, and production in biotechnology companies or laboratories. They typically assist in conducting experiments, analyzing data, preparing samples, and maintaining laboratory equipment. Their work helps develop new products or processes in areas like pharmaceuticals, agriculture, and environmental science. Biotech Associates often have a background in biology, chemistry, or related fields and work under the supervision of scientists or senior researchers.

What are the key skills and qualifications needed to thrive as a biotech associate?

To thrive as a Biotech Associate, you need a solid background in biology, chemistry, or a related field, usually supported by a bachelor's or master's degree. Familiarity with laboratory techniques, data analysis software, and compliance with regulatory standards like GLP or GMP is essential. Strong attention to detail, problem-solving abilities, and effective teamwork are standout soft skills in this position. These skills ensure accurate experimental results, regulatory compliance, and efficient collaboration in fast-paced research environments.

What are some typical challenges faced by biotech associates when working in a laboratory setting?

Biotech Associates often encounter challenges such as troubleshooting complex experiments, maintaining strict adherence to safety protocols, and managing multiple projects simultaneously. Working with sensitive biological materials requires attention to detail and the ability to quickly adapt to unexpected results or equipment malfunctions. Collaboration with scientists and cross-functional teams is frequent, so strong communication skills are essential to ensure experiments are aligned with broader research goals.

What is the difference between Biotech Associate vs Laboratory Technician?

AspectBiotech AssociateLaboratory Technician
Required CredentialsBachelor's degree in biology, biotech, or related field; some roles may require experienceAssociate's degree or relevant certification; less emphasis on advanced degrees
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsAcademic labs, industrial labs, healthcare facilities
Employer & Industry UsageBiotech firms, pharmaceutical companies, research institutionsHospitals, research labs, manufacturing plants
Common Search & ComparisonYesNo

The main difference between a Biotech Associate and a Laboratory Technician lies in their educational requirements and work scope. Biotech Associates typically hold a bachelor's degree and engage in research and development activities within biotech companies or research institutions. Laboratory Technicians often have an associate's degree and focus on routine lab tasks, testing, and sample processing. Both roles are essential in laboratory settings but differ in responsibilities and qualifications.

What are the most commonly searched types of Biotech jobs in New York?

The most popular types of Biotech jobs in New York are:

What are popular job titles related to Biotech Associate jobs in New York?

For Biotech Associate jobs in New York, the most frequently searched job titles are:

What job categories do people searching Biotech Associate jobs in New York look for?

The top searched job categories for Biotech Associate jobs in New York are:

What cities in New York are hiring for Biotech Associate jobs?

Cities in New York with the most Biotech Associate job openings:

Biotech Associate jobs near you
Infographic showing various Biotech Associate job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $45,213 per year, or $21.7 per hour.

Senior Clinical Trial Associate

Legend Biotech US

Somerset, NJ • On-site

$35.50 - $48.25/hr

Full-time

Posted 10 days ago

Key responsibilities

  • Support the execution of complex Phase I/II CAR-T oncology clinical trials by providing operational, administrative, and coordination support.

  • Oversee the preparation, organization, and maintenance of trial documentation, including regulatory files and Trial Master Files (TMFs/eTMFs).

  • Coordinate study meetings, track trial progress, and serve as a liaison between the clinical trial team, vendors, CROs, and investigational sites.

Job description

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases. From our global network of research and development sites, we are committed to discovering and developing safe, effective, and cutting-edge therapies for patients worldwide.
Legend Biotech entered into a global collaboration agreement with Johnson & Johnson to jointly develop and commercialize CARVYKTI® (ciltacabtagene autoleucel; cilta-cel). Through this strategic partnership, we combine complementary expertise and capabilities to advance innovative immunotherapies for patients living with multiple myeloma.
Legend Biotech is seeking a Senior Clinical Trial Associate as part of the Clinical Operations team basedin Somerset, NJ.
Location: Remote
Role Overview
We are seeking a highly skilled and motivated Senior Clinical Trial Associate (Sr. CTA) to join our growing Clinical Operations team to support early-stage clinical development. The Sr. CTA will play a critical role in the execution of complex Phase I/II CAR-T oncology clinical trials by providing high-quality operational, administrative, and coordination support.
The ideal candidate will have substantial experience in clinical trial operations and administration, with a strong understanding of clinical trial processes, regulatory requirements, and GCP. This role is critical to ensuring the efficient execution of clinical trials, maintaining regulatory compliance, and providing operational support to cross-functional study teams.
Key Responsibilities
  • Provide cross-functional administrative and operational support for study team meetings, advisory boards, investigator meetings, and other study-related forums.
  • Support Senior Clinical Trial Managers in the day-to-day execution of complex Phase I and Phase II CAR-T oncology trials, ensuring all activities are conducted in compliance with ICH-GCP and applicable regulatory requirements.
  • Oversee the preparation, organization, and maintenance of trial documentation, including regulatory files, Trial Master Files (TMFs/eTMFs), and study correspondence.
  • Ensure documentation is current, complete, and compliant with ICH-GCP and company SOPs.
  • Assist with the planning, start-up, execution, and close-out of clinical trials, including coordination with clinical sites and support of protocol and regulatory compliance activities.
  • Assist with the preparation, submission, and tracking of regulatory and IRB/IEC documents.
  • Maintain working knowledge of applicable regulations and standards to support ongoing study compliance.
  • Schedule and coordinate study meetings, including investigator meetings, site visits, and internal team meetings.
  • Prepare meeting agendas, document minutes, track action items, and follow up to ensure timely completion.
  • Assist in tracking trial progress, including site activation, enrollment, monitoring activities, and key study milestones.
  • Prepare and maintain study status reports and trackers for internal and external stakeholders.
  • Support data management activities, including query tracking and data reconciliation, in collaboration with Data Management.
  • Serve as a key liaison between the clinical trial team, vendors, CROs, and investigational sites to ensure clear and timely communication.
  • Assist with vendor oversight by tracking deliverables, timelines, and resolving operational issues.
  • Proactively identify operational issues and risks, propose solutions, and escalate to the Senior Clinical Trial Manager or Clinical Operations leadership as appropriate.
  • Contribute to the development and continuous improvement of clinical operations processes and best practices.
  • Provide guidance and mentorship to junior CTAs, sharing best practices and contributing to team capability building.

Requirements
  • Bachelor's degree in life sciences, clinical research, or a related field.
  • Relevant certifications (e.g., CRC, CRA) are a plus.
  • Minimum of 3-5 years of experience as a Clinical Trial Associate or in a similar clinical research role.
  • Demonstrated experience supporting trial coordination, regulatory documentation, and site management activities.
  • Oncology trial experience required; cell therapy and/or CAR-T experience strongly preferred.
  • Strong understanding of ICH-GCP, regulatory requirements, and clinical trial processes.
  • Proficiency with CTMS, eTMF, and EDC systems.
  • Excellent organizational skills with the ability to manage multiple priorities in a fast-paced environment.
  • Strong written and verbal communication skills.
  • Detail-oriented with strong analytical and problem-solving skills.
  • Ability to work independently and collaboratively within cross-functional teams.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and familiarity with eTMF and EDC platforms.

#Li-RP1
#Li-Hybrid
Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.
Work Authorization & Employment Eligibility
Applicants must be authorized to work in the United States. As part of our commitment to maintaining a lawful workforce and ensuring compliance with federal employment regulations, we participate in the E-Verify program. If you are selected for employment, you will be required to complete the Form I-9 process, and your employment eligibility will be verified through E-Verify in accordance with applicable federal law. We are committed to providing a fair, transparent, and welcoming hiring experience for all candidates.
EEO Statement
It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances.
Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company.
For information related to our privacy notice, please review: Legend Biotech Privacy Notice.

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