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$8

$26

$61

How much do openclinica jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for openclinica in the United States is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $30.77 per hour, depending on experience, location, and employer.

What is OpenClinica?

OpenClinica is an open-source software platform used for electronic data capture (EDC) and clinical data management in clinical trials. It allows researchers and organizations to design study forms, collect and manage clinical trial data securely, and comply with regulatory standards. The platform supports both simple and complex studies and is widely used in academic, non-profit, and commercial research settings. OpenClinica also offers tools for data monitoring, audit trails, and integration with other systems.

What are the key skills and qualifications needed to thrive as an OpenClinica specialist?

To thrive as an OpenClinica Specialist, you need a solid understanding of clinical trial processes, data management principles, and experience in electronic data capture (EDC) systems, ideally with a background in life sciences or health informatics. Proficiency in using the OpenClinica platform, familiarity with database query languages like SQL, and knowledge of regulatory compliance (such as GCP) are typically required. Strong analytical thinking, attention to detail, and effective communication skills help ensure accurate data collection and smooth collaboration with research teams. These skills are crucial for maintaining data integrity, supporting regulatory compliance, and enabling successful clinical trial outcomes.

What is the difference between Openclinica vs Clinical Data Coordinator?

AspectOpenclinicaClinical Data Coordinator
CredentialsKnowledge of clinical data management systems, often requires training in Openclinica softwareTypically holds a degree in life sciences or health-related fields; certifications in clinical data management are common
Work EnvironmentWorks primarily with electronic data capture systems in clinical research settingsManages data entry, validation, and quality control in clinical trial environments
Industry UsageUsed by clinical research organizations, pharmaceutical companies, and CROsEmployed in similar settings, focusing on data management and compliance

Openclinica is a specific electronic data capture platform used in clinical trials, while a Clinical Data Coordinator manages data entry, validation, and quality assurance within clinical research projects. Both roles require knowledge of clinical data processes, but Openclinica focuses on software proficiency, whereas the Clinical Data Coordinator emphasizes data management skills.

What are some common challenges faced by OpenClinica professionals when managing clinical trial data, and how can these be addressed?

OpenClinica professionals often encounter challenges such as ensuring data quality, maintaining regulatory compliance, and handling complex study protocols. Managing large volumes of data while adhering to Good Clinical Practice (GCP) guidelines requires attention to detail and strong organizational skills. Collaboration with clinical teams and IT staff is essential to resolve issues related to data integration, user access, and system updates. Staying current with OpenClinica updates and participating in ongoing training can help professionals effectively navigate these challenges and contribute to successful clinical trials.
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Openclinica jobs near you
Infographic showing various Openclinica job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 13% Physical, 7% Hybrid, and 80% Remote job distribution, with an average salary of $54,791 per year, or $26.3 per hour.

Clinical Research Data Associate II - The Angeles Clinic & Research Institute

Cedars Sinai

Los Angeles, CA • On-site

$25.17 - $39.01/hr

Full-time

This job post has expired today. Applications are no longer accepted.

Cedars-Sinai rating

8.6

Company rating: 8.6 out of 10

Based on 131 frontline employees who took The Breakroom Quiz

41st of 1,059 rated hospitals

Job description


Why Cedars-Sinai?
At Cedars-Sinai, we pride ourselves on our inclusive and collaborative culture. We are committed to encouraging an environment where diverse perspectives are valued and innovative ideas can flourish. Our team works together to achieve world-class results, and we support each other in reaching our full potential. If you are looking to grow your career in a place that values excellence and impact, Cedars-Sinai is the perfect place for you.
Join us in our mission to transform healthcare and improve patient outcomes. Apply today and become part of a team that is making a real difference in the world!
Grow your career at Cedars-Sinai!
The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. Our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists work closely together to advance cancer care. We are committed to bringing innovative therapeutic options to all of our patients with cancer.
Join our team and contribute to groundbreaking research!
The Clinical Research Data Associate II manages the data for assigned research studies. This will include, designing forms for data collection, clinical data abstraction, processing data, maintaining record systems, and producing project reports for studies. In addition, may train clinical research staff, perform basic statistical analysis, and work with bioinformatics to develop and maintain trial management systems. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
Key Responsibilities:
  • Coordinates data for research studies.
  • Designs forms for data collection.
  • Performs clinical data collection/abstraction.
  • Processes clinical data using a range of computer applications and database systems to support cleaning and management of subject or patient data.
  • Produces project reports.
  • Performs data searches and other related administrative tasks.
  • Participates in required training and education programs.
  • Works closely with study monitors to review study data and respond to inquiries.
  • Provides support and preparation for study audits.
  • May train clinical research staff to help improve the quality of the data being collected.
  • May solve operational/data problems in consultation with other employees and/or supervisors.
  • May perform basic statistical analysis in conjunction with a biostatistician.

Work Location: This is a hybrid position requiring 4 days per week onsite and 1 day per week remote. Please note that fully remote work arrangements are not available for this position at this time.
Qualifications
Education
  • High School Diploma or GED required
  • Bachelor's degree in a related field (e.g., Life Sciences, Health Sciences, or similar) preferred

Experience
  • Minimum of two (2) years of relevant experience in clinical research or a related setting
  • Hands-on experience with Electronic Data Capture (EDC) systems, preferably within oncology clinical trials
  • Familiarity with EDC platforms such as REDCap, Oracle Clinical, Veeva Vault, Medidata Rave, and/or OpenClinica
  • Proficiency with data management software and related tools
  • Demonstrated ability to work effectively in a collaborative, team-oriented environment
  • Strong attention to detail with excellent organizational and time-management skills
  • Excellent written and verbal communication skills
  • Proven ability to adhere to regulatory requirements and ethical guidelines

Licensure/Certification
  • Certification in Clinical Research (ACRP, SOCRA, or equivalent) preferred

Work Location: This is a hybrid position requiring 4 days per week onsite and 1 day per week remote. Please note that fully remote work arrangements are not available for this position at this time.
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