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Data Integrity Associate 6305 Jobs in Raleigh, NC

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Clinical Research Associate II

Cary, NC · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ... Expertise in monitoring practices, data integrity, and site management, with proficiency in ...

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Clinical Research Associate II

Raleigh, NC · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ... Expertise in monitoring practices, data integrity, and site management, with proficiency in ...

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Clinical Research Associate II

Raleigh, NC · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ... Expertise in monitoring practices, data integrity, and site management, with proficiency in ...

Ubertal Inc.

Microbiologist

Holly Springs, NC · On-site

... associate's and 5+ years of industry experience or equivalent • 3+ years of laboratory experience OR equivalent preferred. • Intermediate knowledge of GMPs, safety regulations and data integrity ...

IQVIA

Clinical Research Associate, IQVIA Biotech

Durham, NC · On-site

$71K - $169K/yr

Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ... Your work will directly contribute to the integrity and quality of clinical research data. Key ...

Pwc

Data Strategy-Manager

Raleigh, NC

$99K - $232K/yr

You are expected to lead with integrity and authenticity, articulating our purpose and values in a ... Associate - SAP Master Data Governance (MDG) - SnowPro Core / SnowPro Advanced - Databricks ...

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All JobsData Integrity Associate 6305 JobsData Integrity Associate 6305 Jobs in Raleigh, NC

Data Integrity Associate 6305 information

See Raleigh, NC salary details

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$54

How much do data integrity associate 6305 jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for data integrity associate 6305 in Raleigh, NC is $32.15, according to ZipRecruiter salary data. Most workers in this role earn between $23.85 and $38.08 per hour, depending on experience, location, and employer.

What is the difference between Data Integrity Associate 6305 vs Data Quality Analyst?

AspectData Integrity Associate 6305Data Quality Analyst
Primary FocusEnsuring data accuracy, consistency, and compliance within databasesAssessing and improving data quality through analysis and reporting
Required SkillsData validation, database management, attention to detailData analysis, quality metrics, reporting tools
Work EnvironmentHealthcare, finance, or corporate data teamsIT departments, data analytics teams
CertificationsTypically none required, but certifications like CDMP may helpData analysis certifications like CAP, CDMP beneficial

While both roles focus on data quality, the Data Integrity Associate 6305 primarily ensures data accuracy and compliance within databases, often in regulated industries. The Data Quality Analyst emphasizes analyzing and improving data quality through metrics and reporting. Both roles require attention to detail and familiarity with data management tools, but their day-to-day tasks and focus areas differ slightly.

What are popular job titles related to Data Integrity Associate 6305 jobs in Raleigh, NC?

For Data Integrity Associate 6305 jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Data Integrity Associate 6305 jobs in Raleigh, NC look for?

The top searched job categories for Data Integrity Associate 6305 jobs in Raleigh, NC are:

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Cities near Raleigh, NC with the most Data Integrity Associate 6305 job openings:

Data Integrity Associate 6305 jobs near you
Infographic showing various Data Integrity Associate 6305 job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 72% In-person, 14% Hybrid, and 14% Remote job distribution, with an average salary of $66,874 per year, or $32.2 per hour.

Experienced Clinical Research Associate - Sponsor Dedicated

Syneos Health, Inc.

Morrisville, NC • On-site

$70 - $100/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 2 days ago

New

Key responsibilities

  • Perform site qualification, initiation, monitoring, management, and close-out activities to ensure regulatory, ICH-GCP, and GPP compliance.

  • Verify source documents, review investigator site files, and ensure data accuracy and query resolution.

  • Serve as primary liaison with site personnel, support site recruitment and retention, and prepare for audit readiness.

Syneos Health rating

8.1

Company rating: 8.1 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

38th of 86 rated pharmaceutical

Job description

Experienced Clinical Research Associate - Sponsor Dedicated

Updated: Yesterday
Location: Morrisville, NC, United States
Job ID:25109784-OTHLOC-1500-2DTX-2DR

Description

Responsible for site qualification, initiation, monitoring, management, and close‑out activities ensuring regulatory, ICH‑GCP and GPP compliance. Performs source document review, data verification, query resolution, IP inventory, investigator site file review, and documentation per SOPs. Provides audit readiness support, site recruitment, retention, and acts as primary liaison with study site personnel. Attends investigator and sponsor meetings and participates in global monitoring/project staff meetings.

Job Responsibilities
  • Perform site qualification, initiation, interim monitoring, site management activities and close‑out visits (on‑site or remotely) ensuring regulatory, ICH‑GCP and/or GPP compliance.
  • Verify informed consent process, protect subject confidentiality, and assess factors affecting safety and data integrity.
  • Assess site processes, conduct source document review, verify CRF data accuracy, resolve queries, and ensure eCRF compliance.
  • Perform IP inventory, reconcile storage/safety, ensure correct dispensing and handling.
  • Review Investigator Site File for accuracy, reconcile with Trial Master File, and ensure archiving compliance.
  • Document activities via letters, reports, logs per SOPs; support recruitment, retention, and data tracking.
  • Manage site‑level activities, budgets, and timelines; adapt to changing priorities.
  • Serve as primary liaison with site personnel; ensure training and compliance.
  • Prepare for and attend investigator and sponsor meetings; participate in training sessions.
  • Provide guidance toward audit readiness and support audit preparation and follow‑up.
  • Maintain knowledge of ICH/GCP Guidelines and company SOPs; complete training as required. (Additional responsibilities include real‑world late‑phase study support, chart abstraction, data collection, hiring junior staff, identifying out‑of‑scope activities, and suggesting potential sites.)
Qualifications
  • Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
  • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
  • Good computer skills and ability to embrace new technologies.
  • Excellent communication, presentation and interpersonal skills.
  • Ability to manage required travel of up to 75% on a regular basis.
  • US ONLY: compliance with deployment medical information requirements as described.
Summary

Roles within Clinical Monitoring/CRA oversee and ensure the integrity of clinical research studies by monitoring data and processes from a centralized location. This includes remote monitoring of trial sites to verify compliance, utilizing data analytics and risk‑based monitoring to identify potential issues, and collaborating with site teams to implement quality enhancements.

Benefits

Benefits may include a company car or car allowance; health benefits including medical, dental, and vision; company match 401(k); participation in Employee Stock Purchase Plan; eligibility to earn commissions/bonuses; and flexible paid time off and sick time. Eligibility for paid sick time may vary by state.

Salary Range

The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.

Equal Employment Opportunity

Syneos Health complies with all applicable federal, state, and municipal laws regarding paid sick time. The Company is committed to compliance with the Americans with Disabilities Act, including providing reasonable accommodations when appropriate.

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