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Clinical Data Associate Remote Jobs in New York (NOW HIRING)

Mondo

Clinical Data Governance Lead

Manhattan, NY · Remote

$77 - $92/hr

Remote (US-Based) EST preferred Start Date Is: July 1st Duration: 6 months Compensation Range: $77/hr - $92/hr W2 Benefits: Eligible for Health, Dental, Vision, 401K Must be authorized to work in the ...

Jj

Manager, Clinical Data Management

Raritan, NJ · On-site +1

Clinical Data Management Job Category: Professional All Job Posting Locations: Horsham ... Remote work options may be considered on a case-by-case basis and if approved by the Company. About ...

IQVIA

Senior Data Team Lead (Remote)

New York, NY · Remote

$86K - $217K/yr

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

IQVIA

Senior Data Team Lead (Remote)

Jersey City, NJ · Remote

$86K - $217K/yr

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

OrganOx

Clinical Project Associate

Madison, NJ · Remote

This is a remote position in the United States. Major Responsibilities Under direction from the ... data collection methods and training materials. · Assist in the development and review of study ...

OrganOx

Clinical Project Associate

Madison, NJ · On-site +1

This is a remote position in the United States. Major Responsibilities Under direction from the ... data collection methods and training materials. • Assist in the development and review of study ...

WES

Grants Associate (Remote)

Manhattan, NY · Remote

$48K - $59K/yr

USA - Remote Compensation: $48K - 59K USD Who We Are: World Education Services (WES) is a ... Data Management and Analysis - 30% * Develop and manage surveys to gather demographic, impact, and ...

MM International

Data Scientist

New York, NY · Remote

Remote Duration 4-6 months The RBQM Data Scientist supports central monitoring and risk-based quality management (RBQM) for clinical trials. This role focuses on implementing and running pre-defined ...

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Clinical Data Associate Remote information

See New York salary details

$14

$45

$98

How much do clinical data associate remote jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for clinical data associate remote in New York is $45.96, according to ZipRecruiter salary data. Most workers in this role earn between $32.16 and $57.60 per hour, depending on experience, location, and employer.

What are some common challenges faced by a clinical data associate working remotely, and how can they be managed?

Clinical Data Associates working remotely often face challenges related to communication and maintaining data quality standards across distributed teams. It can be more difficult to collaborate with clinical research coordinators, data managers, and other stakeholders without in-person interactions, making clear and timely communication essential. Utilizing secure data management platforms, participating in regular virtual meetings, and adhering strictly to data integrity protocols can help address these challenges. Proactively seeking feedback and staying updated on regulatory changes also contribute to maintaining high standards while working remotely.

What is a clinical data associate?

A Clinical Data Associate (Remote) is a professional who manages and verifies data collected during clinical trials, working from a remote location. They ensure the accuracy, integrity, and confidentiality of clinical trial data, collaborating with clinical teams and using specialized software. Their responsibilities include data entry, cleaning, validation, and generating reports to support regulatory submissions. Remote Clinical Data Associates utilize secure systems to access and manage data, allowing them to efficiently support clinical research from anywhere.

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

To thrive as a Clinical Data Associate (Remote), you need a strong background in life sciences, data management, and an understanding of clinical trial processes, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, clinical data management software, and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, problem-solving abilities, and effective virtual communication are crucial soft skills for managing data integrity and collaborating with remote teams. These skills and qualifications ensure the accurate collection, validation, and reporting of clinical trial data, which is essential for regulatory compliance and successful study outcomes.

What is the difference between Clinical Data Associate Remote vs Clinical Data Coordinator?

AspectClinical Data Associate RemoteClinical Data Coordinator
CredentialsBachelor's in life sciences or related field; familiarity with data management systemsBachelor's in health sciences or related field; experience with clinical data
Work EnvironmentRemote, primarily computer-basedTypically on-site or hybrid, working with clinical teams
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites
Search & Comparison IntentYesYes

The Clinical Data Associate Remote and Clinical Data Coordinator roles share similarities in required education and industry usage. However, Clinical Data Associate Remote positions are primarily remote and focus on data entry and management from a distance, while Clinical Data Coordinators often work on-site, coordinating data collection and quality at clinical sites. Both roles are essential in clinical research but differ mainly in work setting and specific responsibilities.

What are popular job titles related to Clinical Data Associate Remote jobs in New York? For Clinical Data Associate Remote jobs in New York, the most frequently searched job titles are:
What job categories do people searching Clinical Data Associate Remote jobs in New York look for? The top searched job categories for Clinical Data Associate Remote jobs in New York are:
What cities in New York are hiring for Clinical Data Associate Remote jobs? Cities in New York with the most Clinical Data Associate Remote job openings:
Clinical Data Associate Remote jobs near you
Infographic showing various Clinical Data Associate Remote job openings in New York as of August 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% Remote job distribution, with an average salary of $95,601 per year, or $46 per hour.

Oncology-CRA/Data Management, Analytics & Statistical Support

BriaCell Therapeutics Corp.

Newark, NJ • Remote

$80K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 16 days ago

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Job description

Hybrid/Remote – Travel Required
We are seeking a flexible and experienced Oncology Clinical Research Coordinator (CRC) or a newly transitioned Clinical Research Associate (CRA) to join our dynamic Clinical Operations team. This hybrid role supports oncology clinical trials and is open to candidates with experience in CROs or academic institutions, even if they lack direct sponsor experience.
In addition to clinical operations expertise, the ideal candidate will bring a strong background in data management, data analytics, and statistical interpretation, with demonstrated experience analyzing clinical trial data to support study execution, monitoring, and decision‐making.
We also welcome international clinical research professionals who are authorized to work in the United States for any employer and bring prior hands‐on experience with U.S.-based clinical research trials and data management.
Remote work flexibility is available, with the expectation that team members adhere to each site's operational policies and requirements. Strong communication skills are essential, with an emphasis on real‐time responsiveness to logistical and operational questions from sites.

Key Responsibilities
Site Monitoring

  • Conduct regular on‐site and remote monitoring visits to ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements
  • Execute monitoring plans tailored to each study
  • Review case report forms (CRFs), source documentation, and data entries for accuracy, completeness, and consistency
  • Identify data discrepancies and collaborate with Data Management to ensure timely query resolution
  • Resolve site-related issues and manage investigational product logistics
  • Maintain strong relationships with site staff and provide real-time support on eligibility, protocol logistics, and operational questions
  • Deliver high-quality presentations during SQVs/SIVs


Data Management, Analytics & Statistical Support

  • Review and interpret clinical trial data to identify trends, risks, and data quality issues
  • Support data cleaning, query management, and reconciliation activities in collaboration with Data Management teams
  • Analyze enrollment trends, protocol deviations, and site performance metrics
  • Apply basic statistical concepts to interpret trial data and support operational decision-making
  • Contribute to development of data tracking tools, dashboards, and performance reports
  • Ensure accuracy and completeness of data within EDC and other clinical systems (CTMS, IRT)
  • Participate in cross-functional data review meetings and support data-driven study execution


Recruitment and Retention Strategies

  • Develop and implement tailored patient recruitment and retention plans using approved vendors
  • Analyze recruitment data and site performance metrics to drive strategic improvements
  • Collaborate with site staff to identify and overcome recruitment barriers
  • Track and report recruitment KPIs and provide actionable insights to the project team
  • Prioritize recruitment support and re-training for underperforming sites
  • Conduct in‐service training and apply engagement strategies to improve enrollment


Communication and Collaboration

  • Serve as the primary point of contact for study sites
  • Collaborate cross-functionally with Clinical Operations, Data Management, Biostatistics, and Regulatory teams
  • Prepare and present study progress reports, including data trends and analytics insights, to stakeholders


Training and Development

  • Train and mentor site staff on protocols, GCP, data entry expectations, and system use (EDC/CTMS)
  • Stay current with industry trends, data management practices, and evolving regulatory expectations


Qualifications

  1. Bachelor’s degree in life sciences, nursing, or related field required
  2. Clinical degree (MD, RN, PharmD, or equivalent).
  3. Experience in data management, clinical data review, and/or data analytics required
  4. Background in statistics, epidemiology, or data analysis strongly preferred
  5. Minimum 2–3 years of oncology clinical research experience (CRC or CRA)
  6. Experience in CROs or academic institutions acceptable in lieu of direct sponsor experience
  7. Strong understanding of GCP, ICH guidelines, and regulatory requirements
  8. Demonstrated ability to interpret clinical trial data and apply analytical thinking
  9. Proficiency with EDC systems, CTMS, and data tracking/reporting tools
  10. Excellent communication, presentation, and problem-solving skills
  11. Ability to respond promptly to site inquiries and logistical needs
  12. Willingness to travel regularly based on monitoring and recruitment requirements

Company Description

BriaCell Therapeutics is a clinical-stage immuno-oncology company developing novel cell-based immunotherapies for solid tumors, including metastatic breast cancer. Our mission is to advance innovative immunotherapy approaches that improve outcomes for patients with difficult-to-treat malignancies.