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Senior Clinical Data Associate Jobs (NOW HIRING)

Eli Lilly and Company

Clinical Data Associate

Indianapolis, IN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Clinical Data Associate is accountable for the end-to-end clinical data sciences delivery for a clinical study, including clinical database build, data acquisition, storage, retrieval, and ...

Discovery Life Sciences

Clinical Data Associate

Huntsville, AL · On-site

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

In this role, the Clinical Data associate will identify potential candidates for research studies based on project specific guidelines, and ensure consistency, integrity, and accuracy of clinical ...

ECOG-ACRIN MRF

Be Seen First

Clinical Data Associate

Boston, MA · On-site

$50K - $62K/yr

  • Medical

  • Dental

  • Life

  • Retirement

The Data Associate is responsible for the quality control of patient data on one or more studies, working with Clinical Research Associates at member institutions, physicians and statisticians ...

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How much do senior clinical data associate jobs pay per year?

As of Aug 15, 2026, the average yearly pay for senior clinical data associate in the United States is $58,937.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,000.00 and $67,500.00 per year, depending on experience, location, and employer.

What are some common challenges senior clinical data associates face when managing large clinical trial datasets?

Senior Clinical Data Associates often manage complex datasets from multiple sites, which can lead to challenges such as ensuring data consistency across sources, resolving discrepancies, and maintaining data integrity under tight timelines. Additionally, they must stay up-to-date with evolving regulatory requirements and work closely with cross-functional teams, including biostatisticians, clinical operations, and data managers, to ensure accurate and timely data delivery. Effective communication, attention to detail, and adaptability are essential to overcome these challenges and ensure successful trial outcomes.

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

To thrive as a Senior Clinical Data Associate, you need expertise in clinical data management, data cleaning, and knowledge of clinical trial processes, supported by a degree in life sciences or a related field. Familiarity with data management systems like Medidata Rave, EDC platforms, and certifications such as CCDM are commonly required. Attention to detail, strong analytical thinking, and effective communication skills help you excel in ensuring data accuracy and collaborating with cross-functional teams. These capabilities are crucial for maintaining data integrity, regulatory compliance, and the overall success of clinical research studies.

What does a senior clinical data associate do?

A Senior Clinical Data Associate is responsible for managing and ensuring the accuracy, integrity, and quality of data collected during clinical trials. They oversee data collection processes, review case report forms, resolve data discrepancies, and ensure compliance with regulatory standards. In addition to performing data management tasks, Senior Clinical Data Associates often mentor junior staff, contribute to developing data management plans, and collaborate with clinical research teams to ensure successful trial outcomes.

What cities are hiring for Senior Clinical Data Associate jobs?

Cities with the most Senior Clinical Data Associate job openings:

What are the most commonly searched types of Senior Clinical Data jobs?

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What states have the most Senior Clinical Data Associate jobs?

States with the most job openings for Senior Clinical Data Associate jobs include:

Senior Clinical Data Associate jobs near you

Clinical Data Associate II

Viking Therapeutics, Inc.

San Diego, CA

$75K - $90K/yr

Full-time

Posted 15 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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