ZipRecruiter

Log In

1

Associate Clinical Data Coordinator Jobs (NOW HIRING)

Maine

Clinical Data Coordinator

Augusta, ME · Hybrid

$17.69 - $24.27/hr

... coordination, and contribute to a program that directly impacts lives. You will: Manage and maintain accurate clinical records, ensuring timely collection and entry of screening and diagnostic data ...

New

Caris Life Sciences

Clinical Data Coordinator I

$64K - $72K/yr

Position Summary The Clinical Data Coordinator is responsible for clinical data entry activities ... Communicate effectively with the research team, investigator(s), Clinical Research Associate(s ...

Caris Life Sciences

Clinical Data Coordinator I

$64K - $72K/yr

Position Summary The Clinical Data Coordinator is responsible for clinical data entry activities ... Communicate effectively with the research team, investigator(s), Clinical Research Associate(s ...

Abbott

Associate Clinical Data Manager

Maple Grove, MN · On-site

The Associate Clinical Data Manager is responsible for performing data management tasks within defined established processes throughout the life cycle of the study including startup, conduct and ...

Abbott

Associate Clinical Data Manager

Maple Grove, MN · On-site

The Associate Clinical Data Manager is responsible for performing data management tasks within defined established processes throughout the life cycle of the study including startup, conduct and ...

next page

Showing results 1-20

All JobsHealthcare JobsMedical Research JobsClinical Data Assistant JobsAssociate Clinical Data Coordinator Jobs

Associate Clinical Data Coordinator information

See salary details

$16

$29

$56

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

As of Sep 13, 2026, the average hourly pay for associate clinical data coordinator in the United States is $29.65, according to ZipRecruiter salary data. Most workers in this role earn between $22.84 and $33.89 per hour, depending on experience, location, and employer.

What does an associate clinical data coordinator do?

An Associate Clinical Data Coordinator is responsible for collecting, managing, and validating clinical trial data to ensure its accuracy and integrity. They work closely with clinical research teams, data managers, and regulatory personnel to support the successful execution of clinical studies. Their tasks include data entry, database maintenance, query resolution, and adherence to regulatory guidelines. This role is essential in ensuring that clinical data is reliable and ready for analysis and reporting.

What are the key skills and qualifications needed to thrive as an associate clinical data coordinator?

To thrive as an Associate Clinical Data Coordinator, you need a solid understanding of clinical research processes, data management principles, and a relevant bachelor's degree—often in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management software, and Good Clinical Practice (GCP) certification is typically required. Strong attention to detail, organizational skills, and effective communication are essential soft skills for ensuring data quality and collaborating with multidisciplinary teams. These competencies are critical to maintain regulatory compliance, ensure accurate clinical trial data, and support successful study outcomes.

What are some common challenges faced by associate clinical data coordinators and how can they be managed effectively?

Associate Clinical Data Coordinators often encounter challenges such as managing large volumes of data, ensuring data accuracy, and meeting tight project deadlines. Effective communication with clinical teams, meticulous attention to detail, and strong organizational skills are essential to overcome these obstacles. Utilizing data management systems and adhering to standard operating procedures can also help ensure smooth workflows and maintain data integrity. Proactive problem-solving and regular training on regulatory requirements further support success in this role.

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

AspectAssociate Clinical Data CoordinatorClinical Data Analyst
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CDMP are a plusRequires a bachelor's or master's degree in data science, statistics, or related field; certifications like CDMP or SAS are common
Work EnvironmentWorks in clinical research settings, hospitals, or pharmaceutical companies, focusing on data collection and managementWorks in research, healthcare, or biotech firms analyzing data to generate insights and reports
Employer & Industry UsageUsed by clinical research organizations, hospitals, and pharma companies for data coordinationEmployed in similar settings but with a focus on data analysis and interpretation

While both roles involve working with clinical data, the Associate Clinical Data Coordinator primarily manages data collection and entry, whereas the Clinical Data Analyst focuses on analyzing and interpreting data to support research and decision-making.

What cities are hiring for Associate Clinical Data Coordinator jobs?

Cities with the most Associate Clinical Data Coordinator job openings:

What states have the most Associate Clinical Data Coordinator jobs?

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

What are popular job titles related to Associate Clinical Data Coordinator jobs?

For Associate Clinical Data Coordinator jobs, the most frequently searched job titles are:

Associate Clinical Data Coordinator jobs near you
Infographic showing various Associate Clinical Data Coordinator 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 $61,666 per year, or $29.6 per hour.

Clinical Data Coordinator

Austin, TX • On-site

Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees
Learn more about Thermo Fisher Scientificexternal

Full-time

Posted 16 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 431 frontline employees who took The Breakroom Quiz

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Able to lift 40 lbs. without assistance, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
Join Us as a Clinical Data Coordinator - Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our expert team, you'll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Clinical Data Coordinator, you will perform all aspects of the data cleaning process, with minimal supervision, in accordance with Good Clinical Practices (GCP) and Standard Operating Procedures/Work Process Documents (SOPs/WPDs), to assess the safety and efficacy of investigational products and/or medical devices.
What You'll Do:
• Supports the setup of study activities such as database design, testing of data entry screens, and Data Validation Manual (DVM) creation, as required.
• Reviews data listings for accuracy and consistency of data.
• Acts as point person and subject matter expert for specialized study-specific processes.
• Generates, tracks and resolves data clarifications and queries and makes changes to the clinical database as required.
• Contributes to the improvement of data management processes on a global level.
• Produces project-specific status reports for management and/or clients on a regular basis.
• Provides training and work direction to junior staff as required.
Education and Experience Requirements:
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
• Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations
• Strong attention to detail and skill with numbers
• Good written and verbal communication skills
• Good analytical/problem-solving skills
• Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
• Strong customer focus and excellent interpersonal skills.
• Proven flexibility and adaptability
• Must be able to set and meet timelines or be able to negotiate schedule changes in response to project demands
• Knowledge of medical/clinical terminology
• Understands project protocol and DVM
• Proven ability in achieving applicable technical competencies per the DM competency grid
Working Conditions and Environment:
• Work is performed in an office environment with exposure to electrical office equipment.
• Occasional drives to site locations
• Occasional travel both domestic and international.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.
Apply today to help us deliver tomorrow's breakthroughs.

What Thermo Fisher Scientific employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply