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Clinical Data Associate Ii Jobs (NOW HIRING)

Rho, Inc.

NY · On-site

We're currently hiring a Clinical Data Associate to join our Federal Research Team! This is a great opportunity to grow your career in the thriving clinical research industry! As a Clinical Data ...

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Clinical Data Associate

Boston, MA · On-site

$50K - $62K/yr

... clinical research experience All positions currently hybrid, working ... 1-2 days/week out of our Boston office. The Data Associate is responsible for the quality control ...

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Clinical Data Associate Ii information

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

As of Sep 10, 2026, the average hourly pay for clinical data associate ii in the United States is $38.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $38.94 per hour, depending on experience, location, and employer.

What does a Clinical Data Associate II do?

A Clinical Data Associate II is responsible for managing and validating clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They review clinical data for completeness, identify discrepancies, and work with other clinical team members to resolve data issues. Their role often includes using specialized databases and software, performing quality checks, and generating reports to support clinical research studies. This position typically requires experience in clinical data management and knowledge of Good Clinical Practice (GCP) guidelines.

What are the key skills and qualifications needed to thrive as a Clinical Data Associate II?

To thrive as a Clinical Data Associate II, you need a strong background in life sciences or related fields, experience in clinical data management, and a keen understanding of regulatory standards. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and often certifications like CDM or GCP are typically required. Attention to detail, problem-solving skills, and effective communication set outstanding professionals apart in this role. These skills are crucial to ensure data integrity, regulatory compliance, and successful clinical trial outcomes.

How does a Clinical Data Associate II typically collaborate with other teams during a clinical trial?

As a Clinical Data Associate II, you will work closely with clinical research coordinators, data managers, biostatisticians, and project managers to ensure the accuracy and integrity of clinical data. Collaboration often involves participating in cross-functional meetings, resolving data discrepancies, and supporting the database lock process. Effective communication and teamwork are essential, as you’ll coordinate data query resolutions and contribute to continuous process improvement with other departments. This collaborative environment provides opportunities to expand your knowledge in clinical research operations and build relationships that can support your career growth.

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Clinical Data Associate Ii jobs near you
Infographic showing various Clinical Data Associate Ii 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 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.

Clinical Data Associate II

San Diego, CA

Viking Therapeutics, Inc.
Pharmaceutical and Medicine Manufacturing • 11 - 50 employees
Learn more about Viking Therapeutics, Inc.external

$75K - $90K/yr

Full-time

Re-posted 10 days ago

Job description

Description

The Clinical Data Associate will contribute to the performance of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, and Standard Operating Procedures (SOPs). Exact title (Clinical Data Associate II or Senior Clinical Data Associate) will depend on experience and skill level.


Essential Duties and Responsibilities 

The main responsibilities of this role include but are not limited to the following:

  • Support Clinical Data Management activities for assigned clinical studies under the direction of the Clinical Data Manager
  • Support the review, maintenance, and filing of study Data Management documentation 
  • Participate in design review of Case Report Forms (CRF) and corresponding CRF Completion Guidelines (CCG) to align with protocol requirements and data collection standards
  • Assist with the testing and maintenance of clinical data systems, including Electronic Data Capture (EDC), Interactive Response Technology (IRT), and Electronic Patient-Reported Outcomes (ePRO)
  • Perform data review activities under the guidance of the Clinical Data Manager, including execution of data checks, query review, and issues tracking
  • Prepare data listings and metrics under the guidance of the Clinical Data Manager
  • Assist with data transfers and reconciliation activities in accordance with defined procedures 
  • Collaborate with cross-functional team members and external to support study activities as directed
  • Track activities and escalate data issues, risks, or delays to the Clinical Data Manager as appropriate 
  • Adhere to Clinical Data Management internal standards and applicable regulatory and industry requirements, including ICH guidelines, Good Practice guidelines (GxP), CDISC standards, and 21 CFR Part 11
  • Other duties as required

Requirements

Education and Experience  

  • Minimum of 1 years of experience in Clinical Data Management (>2 years preferred) 
  • Bachelor's degree or higher in a medical or scientific field 
  • Experienced verbal and written communication skills
  • Preferred: Experienced in clinical data entry system design, development, and maintenance
  • Preferred: Experienced in carrying out data review plans 

Knowledge and Skills 

  • Proficient in Microsoft Office Suite, file sharing software, and online conferencing applications
  • Strong analytical and problem-solving skills
  • Strong verbal and written communication skills
  • Excellent professional interpersonal skills with the ability to work in a positive and collaborative fashion
  • Ability to manage multiple tasks at once and maintain strong attention to detail
  • Self-motivated, dependable individual with self-confidence and a positive attitude

VIKING THERAPEUTICS

Viking Therapeutics, Inc., is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Viking Therapeutics also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.


Notice to Agency and Search Firm Representatives

Viking Therapeutics, Inc. is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Viking employee by a third-party agency and/or search firm without a valid written & signed search agreement, and assignment of specific position, will become the sole property of Viking Therapeutics, Inc. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.


Salary Description

$75,000.00 - $90,000.00 annual salary

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