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Feasibility Associate Jobs in Merrick, NY (NOW HIRING)

... feasibility analyses, and design of mechanical systems. Our engineers are well-versed in all ... LaBella Associates does not accept unsolicited resumes from recruiting professionals or agencies ...

Sr. Mechanical Engineer

Brooklyn, NY · On-site

$80K - $120K/yr

... feasibility analyses, and design of mechanical systems. Our engineers are well-versed in all ... LaBella Associates does not accept unsolicited resumes from recruiting professionals or agencies ...

Retail Designer

New York, NY

$22.50 - $27.25/hr

... the feasibility process. The ideal candidate has a strong foundation in retail design and ... Subject to eligibility requirements, associates may receive health care benefits (including medical ...

Sr. Mechanical Engineer

Brooklyn, NY · On-site

$80K - $120K/yr

... feasibility analyses, and design of mechanical systems. Our engineers are well-versed in all ... LaBella Associates does not accept unsolicited resumes from recruiting professionals or agencies ...

... the feasibility process. The ideal candidate has a strong foundation in retail design and ... Subject to eligibility requirements, associates may receive health care benefits (including medical ...

... feasibility & consulting, owner's representation, sales, partnerships, hospitality, merchandise ... THE ROLE The Cafe Associate is responsible for delivering a world-class guest experience through ...

... feasibility & consulting, owner's representation, sales, partnerships, hospitality, merchandise ... THE ROLE The Café Associate is responsible for delivering a world-class guest experience through ...

Clinical Trial Associate

Manhattan, NY · On-site

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... Support study start-up activities, including site feasibility, investigator onboarding, and ...

Showing results 21-40

Feasibility Associate information

See Merrick, NY salary details

$11

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$33

How much do feasibility associate jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for feasibility associate in Merrick, NY is $20.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.24 and $21.15 per hour, depending on experience, location, and employer.

What is the difference between Feasibility Associate vs Project Coordinator?

AspectFeasibility AssociateProject Coordinator
Required CredentialsBachelor's degree in related field, analytical skillsBachelor's degree, organizational skills
Work EnvironmentResearch-focused, analytical tasksAdministrative, team coordination
Employer & Industry UsageConsulting, healthcare, engineeringConstruction, IT, corporate projects
Common Search & ComparisonYesNo

The Feasibility Associate primarily conducts research and analysis to assess project viability, focusing on data collection and evaluation. In contrast, the Project Coordinator manages project schedules, resources, and communication. While both roles require organizational skills and collaboration, the Feasibility Associate emphasizes analytical assessment, whereas the Project Coordinator handles project execution and logistics.

What job categories do people searching Feasibility Associate jobs in Merrick, NY look for?

The top searched job categories for Feasibility Associate jobs in Merrick, NY are:

Infographic showing various Feasibility Associate job openings in Merrick, NY 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 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $42,317 per year, or $20.3 per hour.

Contractor, Clinical Trial Associate

New York, NY • On-site

Syndax Pharmaceuticals
Biotechnology Research and Development • 51 - 200 employees

$36.75 - $50/hr

Full-time

Re-posted 3 days ago


Job description

Position Description:
The Contractor, Clinical Trial Associate will work with Clinical Operations team to support the conduct of clinical trials. The Clinical Trial Associate may provide support for various clinical trials and may manage certain aspects of the clinical trials. The Clinical Trial Associate will partner with the Clinical Project Managers and Clinical Trial Managers to ensure studies are completed on time, within budget, and in compliance with SOPs, FDA regulations and ICH/GCP guidelines.
Responsibilities and Duties:
  • Maintain the Trial Master Files (TMF): Responsible for the on-going management of the TMF for assigned clinical trials. This is inclusive of receipt, review, QC, tracking and filing of all documents per the Syndax SOPs required within the conduct of assigned clinical trials.
  • Ensure TMF is inspection ready
  • Provide TMF metrics to internal and external stakeholders
  • Work closely with all cross functions to adhere to the trial master oversight plan
  • Assist with the development and maintenance of tracking tools for patient recruitment, site ramp-up, monitoring visits and site payments.
  • Work with Clinical Operations to assist in the oversight of CROs, as appropriate, to ensure the successful conduct of clinical trials, including attending and participating in Clinical Trial Working Groups as needed.
  • Assist in reviewing monitoring visit reports to ensure proper conduct and oversight as needed.
  • Review site-specific Informed Consent Forms
  • Track site feasibility questionnaires
  • Assist in the planning of various meetings and events for the Clinical Operations Team
  • Reconcile invoices to their corresponding contracts and budget and assist with investigator site payments.
  • Prepare and manages study communications including newsletters and study updates
  • Records, prepares and distributes meeting minutes for assigned clinical trials or as designated by the VP of Clinical Operations.
  • Work closely with Clinical Trial Managers to assist with preparation of all external and internal documentation for assigned trials to ensure it's completed in accordance with GCP regulatory requirements and consistent with the study protocol.

Minimum Requirements:
  • Two years' experience in Veeva Vault
  • Two or more years' experience in clinical operations- experience in both a CRO and Sponsor setting desired.
  • Knowledge of FDA regulatory requirements and ICH/GCP guidelines essential
  • Demonstrated efficiency in partnering with CROs and vendors
  • Computer proficiency (Veeva TMF, Word, Excel, PowerPoint, Smart Sheet)
  • Work proactively and efficiently in a fast-paced, high change environment
  • Excellent written and oral communication skills
  • Outstanding organization skills
  • Bachelor's degree desired, preferably in a science or healthcare related discipline

Location: While our corporate headquarters are located in New York City, this position is open to candidates from any location with a preference for east coast locations.
About Syndax:
Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company's pipeline include a menin inhibitor for R/R acute leukemia and a monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment. For more information, please visit www.syndax.com/ or follow the Company on X and LinkedIn.
Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
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