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Associate Clinical Data Analyst Jobs (NOW HIRING)

EDETEK

Clinical Data Analyst

Princeton, NJ · On-site

A Clinical Data Analyst (or Clinical Informatics Analyst) is a clinical research information professional responsible for verifying the validity of clinical trials and data gathered. He/she will ...

R3TEK

Clinical Data Analyst

Hillsborough, NJ

R3 Technology Inc. seeks Clinical Data Analyst for it Hillsborough NJ office. Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on ...

R3tek

Clinical Data Analyst

Hillsborough, NJ · On-site

R3 Technology Inc. seeks Clinical Data Analyst for it Hillsborough NJ office. Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on ...

EDETEK

Clinical Data Analyst

Princeton, NJ · On-site

A Clinical Data Analyst (or Clinical Informatics Analyst) is a clinical research information professional responsible for verifying the validity of clinical trials and data gathered. He/she will ...

UAB

CLINICAL DATA ANALYST

Tampa, FL

$21.10 - $34.30/hr

CLINICAL DATA ANALYST University of Alabama at Birmingham Under general supervision, designs and implements data management systems for clinical information. General Responsibilities * Develops ...

Abbott

Associate Clinical Data Manager

Maple Grove, MN · On-site

The Associate Clinical Data Manager is responsible for performing data management tasks within ... Partner closely with Data Review Management, Study Database Manager, and Data Analytics and Systems ...

UAB NOVA RENT

CLINICAL DATA ANALYST

Birmingham, AL · On-site

$21.10 - $34.30/hr

CLINICAL DATA ANALYST University of Alabama at Birmingham Under general supervision, designs and implements data management systems for clinical information. General Responsibilities * Develops ...

Abbott

Associate Clinical Data Manager

Maple Grove, MN · On-site

The Associate Clinical Data Manager is responsible for performing data management tasks within ... Partner closely with Data Review Management, Study Database Manager, and Data Analytics and Systems ...

EDETEK

Clinical Data Analyst

Princeton, NJ · On-site

AClinicalDataAnalyst's primary responsibility is to ensure that data is accurate and reliable throughout the clinical trial conduct, analysis, and regulatory submission. The information collected and ...

EDETEK, Inc.

Clinical Data Analyst

Princeton, NJ · On-site

AClinicalDataAnalyst's primary responsibility is to ensure that data is accurate and reliable throughout the clinical trial conduct, analysis, and regulatory submission. The information collected and ...

Paradigminfotech

Clinical Data Analyst

Edison, NJ · On-site

... data Continually increase subject matter knowledge on our products Interact with other teams to ... NET Sound analytical, organizational and planning skills and the ability to achieve multiple team ...

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Associate Clinical Data Analyst information

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

As of Sep 12, 2026, the average hourly pay for associate clinical data analyst in the United States is $36.36, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $42.07 per hour, depending on experience, location, and employer.

What does an associate clinical data analyst do?

An Associate Clinical Data Analyst is responsible for collecting, managing, and analyzing clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They typically work closely with clinical research teams to support data entry, data cleaning, and the preparation of reports. Their work is essential in helping organizations make informed decisions about the safety and efficacy of medical treatments, devices, or drugs. This entry-level role often serves as a foundation for more advanced positions in clinical data management or biostatistics.

What are some common challenges faced by associate clinical data analysts when working with clinical trial data?

Associate Clinical Data Analysts often encounter challenges such as managing large volumes of complex clinical trial data, ensuring data accuracy and consistency, and adhering to strict regulatory standards. They may also need to resolve discrepancies found during data cleaning and work collaboratively with clinical research teams to clarify ambiguous data points. Staying organized and maintaining clear communication with colleagues are key to overcoming these challenges and ensuring high-quality data for analysis.

What are the key skills and qualifications needed to thrive as an associate clinical data analyst, and why are they important?

To thrive as an Associate Clinical Data Analyst, you need a solid background in life sciences, statistics, or a related field, often supported by a bachelor’s degree. Familiarity with data management systems like EDC (Electronic Data Capture), statistical software such as SAS or R, and regulatory standards is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for interpreting data and collaborating with cross-functional teams. These competencies ensure accurate data analysis, regulatory compliance, and the successful execution of clinical research studies.
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Associate Clinical Data Analyst jobs near you
Infographic showing various Associate Clinical Data Analyst job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $75,625 per year, or $36.4 per hour.

Associate Clinical Data Manager

Maple Grove, MN • On-site

Siro Clinpharm Pvt Ltd
See more jobs at Siro Clinpharm Pvt Ltdexternal

Other

Posted 8 days ago

Job description

Associate Clinical Data Manager
Location : Maple Grove, MNRole Summary

The Associate Clinical Data Manager supports the planning and execution of clinical study data management activities. Under the direction of a manager, this role leads cross-functional teams through case report form development, database setup, data review, and data cleaning processes to ensure the integrity and quality of clinical study data throughout the lifecycle of an investigation.

Key Responsibilities

• Leads cross-functional teams during protocol development to identify and document data critical to the reliability of

study results and protection of human subjects.

• Manages the development and revision of case report forms (CRF), edit checks, data listings, and clinical

database setup.

• Identifies and evaluates residual risks to critical study data; oversees development of additional mitigations

including focused data cleaning, quality activities, and targeted site instructions.

• Leads the Clinical Project Team through CRF development and partners with the Study Database Manager

through database development, release, programming, and testing of edit checks.

• Conducts review and analysis of subject data as it accumulates, resolving discrepant or aberrant data points via

queries to study sites.

• Identifies systemic or significant data quality issues requiring escalation; manages escalation in partnership with

Project Management, Site Management, Clinical Science, Biometrics, and Safety.

• Manages progress toward data cleaning and data freeze/lock targets for regulatory submission.

• Manages issuance and resolution of discrepancies over the study lifecycle, including root cause analysis and

development of system-level countermeasures and process improvements.

• Leads proactive partnership with field and study team personnel, presenting findings from central monitoring and

data review activities.

• Assists in ongoing risk evaluation through in-depth review of protocol and plan documentation, validation of risk

findings, and development of process-based controls.

• Contributes to the maintenance of data review standards and best practices.

Required Qualifications

• Bachelor’s degree in Biology, Health Sciences, Mathematics, Computer Science, or equivalent field.

• Minimum 5 years of experience in clinical operations or a healthcare-related field.

• Knowledge of Good Clinical Practice (Google Cloud Platform) and global regulations for investigational studies.

• Strong analytical and critical thinking skills with demonstrated data management experience.

• Strong written and verbal communication skills; ability to lead discussions and manage complex regulated studies.

• Ability to effectively influence cross-functional team decisions.

Preferred Qualifications

• Certified Clinical Data Manager (CCDM) designation.

 

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