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Clinical Operations Associate Jobs in Queens, NY

Alpaca Health

Revenue Operations Associate

New York, NY · Remote

$60K - $90K/yr

We help clinicians launch and scale their own clinics by providing AI-powered software, payer ... Role: Revenue Operations Hire Alpaca Health is looking for a Revenue Operations hire to own the ...

Alpaca Health

Revenue Operations Associate

New York, NY · On-site +1

$60K - $90K/yr

We help clinicians launch and scale their own clinics by providing AI-powered software, payer ... Role: Revenue Operations Hire Alpaca Health is looking for a Revenue Operations hire to own the ...

Camber

Insurance Operations Associate

New York, NY · On-site

$80K - $90K/yr

Everyone on Camber's team cares deeply about helping clinicians and patients. 2) We have to have a ... Work directly with operations, billing, engineering, and data entry teammates to inform insurance ...

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All JobsClinical Operations Associate JobsClinical Operations Associate Jobs in Queens, NY

Clinical Operations Associate information

See Queens, NY salary details

$11

$27

$55

How much do clinical operations associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical operations associate in Queens, NY is $27.39, according to ZipRecruiter salary data. Most workers in this role earn between $18.56 and $31.59 per hour, depending on experience, location, and employer.

What is a clinical operations associate?

A Clinical Operations Associate supports the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. They assist in coordinating trial logistics, managing documentation, and communicating with study sites and stakeholders. Their role helps ensure studies run efficiently, meet regulatory requirements, and generate reliable data for drug development and approvals.

What are the typical responsibilities and team dynamics for a clinical operations associate?

As a Clinical Operations Associate, your typical responsibilities include coordinating study activities, maintaining trial documentation, supporting regulatory submissions, and ensuring adherence to protocols and timelines. You will often work as part of a multi-disciplinary team that includes clinical research coordinators, data managers, and study monitors, frequently communicating with internal and external stakeholders to keep the study on track. Collaboration and adaptability are key, as priorities can shift based on site needs or regulatory updates. This role offers valuable exposure to the operations side of clinical research and can serve as a springboard to more senior roles such as Clinical Project Manager or Clinical Research Associate.

What are the key skills and qualifications needed to thrive in the clinical operations associate position, and why are they important?

To thrive as a Clinical Operations Associate, you need a solid background in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills that help manage complex studies and collaborate with cross-functional teams. These abilities are crucial for ensuring that clinical trials run smoothly, meet regulatory standards, and maintain participant safety.

What are the most commonly searched types of Clinical Operations jobs in Queens, NY?

The most popular types of Clinical Operations jobs in Queens, NY are:

What are popular job titles related to Clinical Operations Associate jobs in Queens, NY?

For Clinical Operations Associate jobs in Queens, NY, the most frequently searched job titles are:

What job categories do people searching Clinical Operations Associate jobs in Queens, NY look for?

The top searched job categories for Clinical Operations Associate jobs in Queens, NY are:

What cities near Queens, NY are hiring for Clinical Operations Associate jobs?

Cities near Queens, NY with the most Clinical Operations Associate job openings:

Clinical Operations Associate jobs near you
Infographic showing various Clinical Operations Associate job openings in Queens, NY as of July 2026, with employment types broken down into 90% Full Time, and 10% Part Time. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $56,961 per year, or $27.4 per hour.

Contractor, Clinical Trial Associate

PTC Therapeutics

Warren, NJ • On-site

$35 - $58/hr

Full-time

Posted 6 days ago

Job description

PTC Therapeutics is a global commercial biopharmaceutical company. For over 25 years our team has been deeply committed to a unified purpose: Extending life's moments for children and adults living with a rare disease.
At PTC, we cultivate an inclusive culture where everyone feels valued, respected, and empowered. We welcome candidates from all backgrounds to join our team, fostering a strong sense of belonging.
Visit our website to learn more about our company and culture!
Site: www.ptcbio.com
Job Description Summary:
Job Description:
The Clinical Trial Associate (CTA) supports the Clinical Operations Excellence (COE) function within the Clinical Operations department. This role provides day-to-day operational and administrative support to COE teams across Standards, Inspection Preparedness and Readiness (IPR), Systems, and Vendor Alliance, helping ensure consistent processes, inspection-ready documentation practices, and effective use of clinical operations technologies.
The Clinical Trial Associate (CTA) supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.
ESSENTIAL FUNCTIONS
  • Coordinate and track general COE initiatives, deliverables, and timelines
  • Coordinate working group logistics (meeting scheduling, agendas, minutes, action item tracking) for COE activities.
  • Maintain COE-controlled repositories (e.g., COE mailbox, SharePoint/Teams sites) to ensure content is organized, searchable, and current
  • Support creation and upkeep of best practices, job aids, FAQs, and onboarding materials for Clinical Operations staff.
  • Assist with the development, formatting, publishing, and periodic review of Clinical Operations standards, templates, tools, and guidance documents.
  • Manage controlled documents and records relevant to COE (e.g., version control, distribution lists, archive/retention support).
  • Support IPR/TMF IPR activities with eTMF, such as periodic quality checks, completeness checks, and reconciliation support under direction of SMEs.
  • Support inspection-readiness activities, including tracking deliverables, maintaining readiness checklists, and monitoring action items.
  • Coordinate mock inspection or readiness meeting logistics and support follow-up documentation.
  • Help maintain centralized inspection-readiness resources and ensure consistent filing/naming conventions.
  • Support CAPA and issue tracking activities by maintaining logs, status updates, and meeting minutes, as directed.

COE Systems Support
  • Provide administrative support for clinical systems used by Clinical Operations (e.g., user access request coordination, training coordination, and basic user support triage)..
  • Support system-related change management activities (e.g., communication drafts, training session logistics, and attendance tracking).
  • Ensure work is performed in compliance with applicable SOPs, GCP, internal standards, and data integrity expectations.
  • Interface effectively with department stakeholders to support COE initiatives.

KNOWLEDGE/SKILLS/ABILITIES REQUIRED
* Minimum level of education and years of relevant work experience.
  • Bachelor's degree in a relevant discipline and a minimum of 5+ years of clinical operations and/or clinical trial operations experience within the biotechnology or pharmaceutical industry.

* Special knowledge or skills needed and/or licenses or certificates required.
  • Working knowledge of ICH-GCP, clinical trial documentation practices, and inspection readiness concepts.
  • Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects.
  • High attention to detail and comfort working with metrics, dashboards, and data quality checks.
  • Proficiency in Microsoft Office (Excel, PowerPoint, Word) and familiarity with clinical systems (e.g., CTMS, eTMF, eLearning/LMS).
  • Effective written and verbal communication; able to draft clear meeting minutes, status summaries, and user communications.
  • Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.
  • Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.
  • Continuous improvement mindset; able to identify gaps, propose practical enhancements, and follow through.

* Travel requirements
  • 20-30%

Expected Hourly Range:
$35 - $58/hour. The hourly salary offered will be contingent on assessment of the candidate's education level, background, and experience relative to the requirements of the position they are being considered for, as well as review of internal equity.
#LI-DNI
EEO Statement:
PTC Therapeutics is an equal opportunity employer. We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.
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