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Redcap Data Manager Jobs in California (NOW HIRING)

... data needed for conference presentations, publications, and grant proposals. You will collaborate ... REDCap as well as an in-depth understanding of appropriate laboratory/clinical science or ...

Oversee research databases, ensuring data accuracy, integrity, reporting efficiency, and ... Experience with REDCap as well as an in-depth understanding of appropriate laboratory/clinical ...

... data management and basic analysis (e.g., entering data in REDCap, checking data quality, preparing spreadsheets, running simple scripts or analyses with supervision). Study Operations ...

... data management and basic analysis (e.g., entering data in REDCap, checking data quality, preparing spreadsheets, running simple scripts or analyses with supervision). Study Operations ...

Clinical Research Coordinator

Stanford, CA · On-site

$28.50 - $38/hr

Schedule and monitor study visits, collect biospecimens, and ensure timely and accurate data entry ... REDCap, eProtocol, OnCore, SeRA). * Knowledge of IRB processes, budget management, and sponsor ...

Electronic medical record data * REDCap * Reference management * Protected health information and research confidentiality * Safe handling of blood samples * Scientific writing and manuscript ...

Electronic medical record data * REDCap * Reference management * Protected health information and research confidentiality * Safe handling of blood samples * Scientific writing and manuscript ...

Showing results 21-40

Redcap Data Manager information

What is a Redcap data manager?

Redcap Data Managers are professionals responsible for designing, implementing, and maintaining databases using the REDCap (Research Electronic Data Capture) platform. They ensure data integrity, manage user access, provide technical support, and oversee data collection processes in research studies or clinical trials. Their role often includes training research staff, troubleshooting issues, and ensuring compliance with data security and regulatory standards. Redcap Data Managers play a vital part in facilitating accurate and efficient data management for research projects.

How does a Redcap data manager collaborate with research teams to ensure data quality and compliance?

A Redcap Data Manager works closely with principal investigators, research coordinators, and IT staff to design, implement, and maintain data collection instruments within the REDCap system. They regularly communicate with team members to provide training, troubleshoot issues, and ensure proper data entry protocols are followed. Additionally, they play a vital role in monitoring data for accuracy, managing user permissions, and ensuring compliance with institutional and regulatory standards such as HIPAA. This collaborative environment helps foster reliable data collection and supports successful research outcomes.

What are the key skills and qualifications needed to thrive as a Redcap data manager, and why are they important?

To thrive as a Redcap Data Manager, you need expertise in data management, database design, and an understanding of research protocols, often supported by a degree in health informatics, information science, or a related field. Proficiency with the REDCap platform, knowledge of data security practices, and sometimes familiarity with statistical software or programming languages like SQL are typically required. Strong attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies ensure accurate data collection, compliance with research standards, and seamless collaboration with research teams.

What are popular job titles related to Redcap Data Manager jobs in California?

For Redcap Data Manager jobs in California, the most frequently searched job titles are:

What cities in California are hiring for Redcap Data Manager jobs?

Cities in California with the most Redcap Data Manager job openings:

Infographic showing various Redcap Data Manager job openings in California as of August 2026, with employment types broken down into 81% Full Time, and 19% Part Time. Highlights an 94% In-person, and 6% Hybrid job distribution.

Clinical Research Data Associate II (Hybrid)- The Angeles Clinic & Research Institute

Cedars Sinai

Los Angeles, CA • Hybrid

Full-time

Posted 25 days ago


Cedars-Sinai rating

8.6

Company rating: 8.6 out of 10

Based on 131 frontline employees who took The Breakroom Quiz

44th of 1,066 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.

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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