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Clinical Data Associate Jobs in Peekskill, NY (NOW HIRING)

NS Pharma Inc

Director, Clinical Research

Paramus, NJ · On-site

$210K - $240K/yr

Oversee the tracking of clinical data, regulatory documents, and patient enrollment information and ... Supervise two (2) or three (3) Senior Clinical Study Managers and one Associate Director; including ...

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Clinical Data Associate information

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$14

$40

$90

How much do clinical data associate jobs pay per hour?

As of Jul 31, 2026, the average hourly pay for clinical data associate in Peekskill, NY is $40.70, according to ZipRecruiter salary data. Most workers in this role earn between $30.62 and $40.67 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Data Associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

Which is better, CDM or SAS?

For a Clinical Data Associate, SAS is a widely used software for data analysis and reporting in clinical trials, while CDM (Clinical Data Management) refers to the overall process of collecting, cleaning, and managing clinical data, often using various tools including SAS. SAS skills are highly valued in the role, but understanding the broader CDM process is also important for effective data handling and compliance.

What's next after CRC?

After working as a Clinical Research Coordinator (CRC), professionals often advance to roles such as Clinical Data Associate, Clinical Trial Manager, or Regulatory Affairs Specialist. Gaining experience, certifications like CCRP, and developing skills in data management and regulatory compliance can facilitate career progression in clinical research.

What are the key skills and qualifications needed to thrive as a Clinical Data Associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What does a Clinical Data Associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What is the role of a clinical data associate?

A clinical data associate is responsible for collecting, managing, and ensuring the accuracy of data from clinical trials. They review data for completeness, resolve discrepancies, and use database tools to support data integrity and regulatory compliance throughout the trial process.

What Does a Clinical Data Associate Do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

Do you need a degree to be a CRC?

A Clinical Data Associate (CDA) typically does not require a specific degree, but a background in life sciences, healthcare, or related fields is often preferred. Many employers value relevant certifications and experience with clinical data management tools. Educational requirements can vary by employer and job level.

Is CRA an entry level job?

A Clinical Data Associate (CDA) role is typically considered an entry-level position in clinical research, often requiring a bachelor's degree in a related field and some familiarity with data management tools. However, a Clinical Research Associate (CRA) role usually requires more experience and is considered a mid- to senior-level position, involving site monitoring and regulatory compliance. Entry-level roles may serve as a stepping stone toward CRA positions with additional experience and certifications.

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

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

More about Clinical Data Associate jobs
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What cities near Peekskill, NY are hiring for Clinical Data Associate jobs? Cities near Peekskill, NY with the most Clinical Data Associate job openings:
Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Peekskill, NY as of July 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $84,663 per year, or $40.7 per hour.

Oncology Clinical Data Specialist (JR230552)

Montefiore

Tarrytown, NY • On-site

Other

Re-posted 18 days ago

Job description

IntroductionTo heal, to teach, to discover and to advance the health of the communities we serve.

To learn more about the “Montefiore Difference” – who we are at Montefiore and all that we have to offer our associates, please click here. 

OverviewThe Oncology Clinical Data Specialist must review the data for use by the Montefiore Cancer Program to ensure that data regarding incidence of cancer by primary site,  trends, morphology,  stage at diagnosis, survival rate, treatment modalities and other variables are of the highest quality for use in patient care research and education and is abstracted completely and accurately.

ResponsibilitiesThe Oncology Clinical Data Specialist  is responsible  to ensure that the data abstracted is accurate and complete and meets the requirements of both NYS and National Cancer Data submission requirements.
The Specialist must understand case finding techniques, abstracting rules, morphology of the disease, staging criteria, treatment modalities, research protocols  and survivorship requirements to provide meaningful data reporting and feed  back to the Montefiore Cancer Program Committee and to prepare for Accreditation surveys 
The Specialist must collaborate with physician, nursing and other clinical staff on patient data accuracy, completeness, survey readiness  and documentation requirements and provide guidance and coaching on cancer registry data and requirements as required.   

Requirements

  • High School Diploma or GED required
  • Bachelors Preferred
  • Certification as a Certified Tumor Registrar (CTR) as a Oncology Data Specialist(ODS) is required.
  • Candidates for this position must have satisfactorily completed a course in Cancer Registry operations/abstraction including abstracting and Staging of cases, coding using ICD-O and other applicable classifications.  
  • 3 Years of applicable experience preferred.
  • Candidates must demonstrate strong combination of education/knowledge/experience in use of Cancer Registry Operations and Standards Manual.  
  • Must demonstrate familiarity with practices and guidance of national standard setters such as: CoC, SEER, NAACCR, ICD-O, AJCC and other industry standards and methodologies.   
  • Knowledge of State and National regulations and guidelines for Cancer Registries, CoC accredited cancer programs and cancer reporting 
  • Familiarity with reviewing medical records in an electronic environment. 
  • Critical thinking and excellent communication and problem solving skills 
  • Knowledge of data manipulation and analysis preferred.  
  • Relevant combination of Education, Knowledge and Experience will be considered  

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