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Crf Jobs in Riverside, CA (NOW HIRING)

Collabera

Clinical Data Manager

Irvine, CA

Ensure study data quality by CRF data review, preparation for entry, query processing, discrepancy management, ad-hoc reporting, listing generation. Create and maintain all essential data management ...

JenaValve

Specialist, Clinical Safety

Irvine, CA · On-site

$100K/yr

Lead site CRF development for AE Main Forms and AE Sub-forms; review edit checks and provide input into other CRF form development as needed. * Support PMA/APR activities including query closure ...

Choc

CT Technologist Lead

Orange, CA

$57.70 - $71.84/hr

California Fluoroscopy Certification (CRF); Venipuncture Certificate Work Environments - Functional Demand: Sedentary - Very light energy level Lift 10 lbs. box overhead. Lift and carry 15 lbs. Push ...

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Crf information

See Riverside, CA salary details

$8

$28

$56

How much do crf jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for crf in Riverside, CA is $28.20, according to ZipRecruiter salary data. Most workers in this role earn between $9.70 and $46.09 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Fellow (CRF), and why are they important?

To thrive as a Clinical Research Fellow, you typically need a medical degree or relevant scientific background and a strong foundation in clinical research methodologies and data analysis. Familiarity with statistical software, electronic data capture systems, and Good Clinical Practice (GCP) certification is often required. Excellent communication, attention to detail, and strong organizational skills are crucial for effective collaboration and study management. These skills ensure the integrity, reliability, and success of clinical research projects while maintaining compliance with ethical standards.

What are some common challenges faced by Clinical Research Facilitators (CRFs) when coordinating clinical trial activities, and how can these be managed?

Clinical Research Facilitators (CRFs) often encounter challenges such as managing complex schedules, ensuring regulatory compliance, and maintaining clear communication among multidisciplinary teams. Balancing the needs of researchers, participants, and regulatory bodies can be demanding, particularly when timelines are tight or protocols change. Successful CRFs rely on strong organizational skills, attention to detail, and proactive communication to anticipate issues and coordinate solutions. Utilizing project management tools and fostering collaborative relationships across departments can help mitigate these challenges and ensure the smooth progress of clinical trials.

What are CRFs in clinical research?

CRFs, or Case Report Forms, are specialized documents used in clinical research to systematically collect data from each participant in a clinical trial. They serve as a tool for recording information required by the study protocol, including patient demographics, treatment details, and study outcomes. CRFs can be paper-based or electronic (eCRFs), and their accuracy is critical to ensuring the reliability and integrity of clinical trial data. Researchers and clinical staff use CRFs to ensure consistent data collection and facilitate regulatory compliance throughout a study.

What is the difference between Crf vs Clinical Research Coordinator?

AspectCrfClinical Research Coordinator
CredentialsTypically requires knowledge of case report forms, data management, and clinical trial documentationRequires knowledge of study protocols, patient interaction, and regulatory compliance
Work EnvironmentData management and documentation in clinical trial settingsDirect patient interaction and site management in clinical trials
Employer & Industry UsageUsed mainly in clinical data management and pharmaceutical researchCommonly employed at clinical trial sites, hospitals, and research organizations

While both Crf and Clinical Research Coordinator roles are integral to clinical trials, Crf focuses on data collection and management through case report forms, whereas the Clinical Research Coordinator handles patient interactions, site coordination, and study compliance. Understanding these differences helps in choosing the right career path or job search focus within clinical research.

What job categories do people searching Crf jobs in Riverside, CA look for? The top searched job categories for Crf jobs in Riverside, CA are:
Crf jobs near you
Clinical Data Manager

Clinical Data Manager

Collabera

Irvine, CA

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago

Job description

Company Description

About Collabera:
Established in 1991, Collabera is one of the fastest growing end-to-end information technology services and solutions companies globally. As a half a billion dollar IT company, Collabera's client-centric business model, commitment to service excellence and Global Delivery Model enables its global 2000 and leading mid-market clients to deliver successfully in an increasingly competitive marketplace.
With over 8200 IT professionals globally, Collabera provides value-added onsite, offsite and offshore technology services and solutions to premier corporations. Over the past few years, Collabera has been awarded numerous accolades and Industry recognitions including.
Collabera awarded Best Staffing Company to work for in 2012 by SIA. (hyperlink here)
Collabera listed in GS 100 - recognized for excellence and maturity
Collabera named among the Top 500 Diversity Owned Businesses
Collabera listed in GS 100 & ranked among top 10 service providers
Collabera was ranked:
32 in the Top 100 Large Businesses in the U.S
18 in Top 500 Diversity Owned Businesses in the U.S
3 in the Top 100 Diversity Owned Businesses in New Jersey
3 in the Top 100 Privately-held Businesses in New Jersey
66th on FinTech 100
35th among top private companies in New Jersey
http://www.collabera.com/about_us/accolades.jsp
Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance.

Job Description

Position Title: Clinical Data Manager

Location: Irvine, CA USA 92618

Duration: 12 months (Strong Possibility of Extension)

Employment Type: W2 Contingent Worker


SUMMARY OF POSITION: 

As a key member of the Global Medical Affairs team representing our client's Clinical Operations, this person has responsibility for: 

Member of clinical research team responsible for data management activities across multiple trials.

Main responsibility includes design of Case Report Forms, development of edit check specifications, creation of test scripts and testing of study database, query processing, data reporting, putting in place data management plans, timelines and manage multiple projects through closeout and archiving.

Activities also include assisting/leading with study start-up activities like training sites, internal users and attendance in clinical project meetings.

ESSENTIAL FUNCTIONS: 

Perform data management activities on both Electronic Data Capture (EDC) and paper studies. Major activities include 

Performs as lead data manager for projects and/or programs

Responsible for the design and development of Case Report Forms (CRF) in collaboration with CRAs or Clinical Project/Program Managers.

Work closely with clinical project team and database programmers to provide edit check requirements and specifications at the time of study database development and Post production changes.

Ensure study data quality by CRF data review, preparation for entry, query processing, discrepancy management, ad-hoc reporting, listing generation.

Create and maintain all essential data management documentation including, but not limited to, data management plans, Data Review guidelines, CRF completion guidelines, Data Entry guidelines, UAT plans and other study specific work instructions or guidelines for multiple projects.

Perform study user acceptance testing and database QC.

Collaborate with CDMs and other staff as necessary

Act as a point of contact with vendors such as Database developers, coders, Safety personnel, QA, Core Labs, etc.

Assist in overall project tasks such as process flowcharts, Standard Operating Procedures (SOP), work instructions, training guidelines, etc.

Participate in project meetings to give a status update to project managers and upper management.

Collaborate with Medical coder to ensure accurate and consistent clinical reporting of clinical terms to assign a validated terminology in prep for analysis and reporting to regulatory authorities

Ensure good Clinical Data Management practices to support data quality and audit readiness.

Ensure necessary data exchanges have occurred as scheduled.

DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS: 

Clinical Database Systems Knowledge - EDC and Paper

Intermediate to Advanced level proficiency with relational databases in either paper or electronic data capture (EDC) systems. 

Big-picture and detail-oriented view of data management processes, tools and procedures.

Product Knowledge/Therapeutic Expertise

Seek out adequate training on products and therapeutic areas in alignment with assigned studies and ensure proper training documentation is completed/maintained.

Basic ability to contribute and/or interpret protocol to create CRFs and edit check spec

Becoming aware of and participating in more standardization of objects and processes, e.g., design of standard case report forms, reusable edit check specifications, study data management metrics, templates as well as data management timeline templates across studies to gain efficiencies in data collection and reporting.

Understanding of regulations (ex. ICH and GCP) and clinical terminology

Overall understanding of regulations (e.g., ICH, GXP, ISO) and more advanced understanding of FDA, GXP and Quality audits that involve Data Management, if required.

Analytical skills (output interpretation)

Intermediate/skill/knowledge in adhoc data reporting, data review listing development, metrics reporting, distribution and review. Sufficient understanding of key analytical end point needs, contributes to review of draft/ final tables, listings, figures and review of interim/final clinical study reports (where applicable). 

Knowledge of coding process and coding tools.

Knowledge of coding process (performed by Medical Coder).

Oversight of major data management activities includes - communicating study specific coding needs and timing to the Coding Specialist. Ensures the exchange of data between the clinical database and the coding tool is set to run on a regular schedule (e.g., nightly, weekly, etc.). 

Ensures coding reviews/discrepancy actions are applied by the Coding Specialist and Data Management as needed.

Written and verbal communication skills (for documentation and customer interaction).

Proficiency in organizational skills and attention to detail to clearly and succinctly write and verbalize in a variety of communication inter-office and remote settings and styles (e.g., documentation, general correspondence, presentations, meetings, trainings etc.). 

Also oversees and assists in preparation of study material for investigator, study coordinator and monitor meetings, if applicable.

Other duties as assigned.

MINIMUM REQUIREMENTS:

Education and Experience:

Bachelor's Degree and a minimum of 3-5 years related experience in a medical device and/or pharmaceutical data management environment. 

Education in Sciences preferred.

Skills/Qualifications:

Computer proficiency in MS Word, Excel, PowerPoint, Access, ORACLE Clinical, Clindex, CRF design tools etc.

Proficient Data management skills on various types of clinical trials (Pharma and/or Device)

Experience with OC Remote Data Capture (RDC) or other EDC systems preferred.

Experience with reporting tools (e.g. TOAD, Discoverer, Crystal Reports, Clindex Reports, etc.) 

Comply with written procedures, instructions, SOPs and other documents

NormLab2 Plus or other lab normal processing systems experience preferred

Excellent organizational skills and attention to detail

ORGANIZATIONAL RELATIONSHIPS/SCOPE:

Will work primarily within Clinical Affairs but may have to interact with the Quality and Regulatory Affairs staff.  

May interact with outside vendors. 

Scope will include multiple clinical studies at a time.

WORKING CONDITIONS:

Normal office conditions. Minimal travel may be required (10-20%).


Qualifications

Computer proficiency in MS Word, Excel, PowerPoint, Access, ORACLE Clinical, Clindex, CRF design tools etc.

Proficient Data management skills on various types of clinical trials (Pharma and/or Device)

Experience with OC Remote Data Capture (RDC) or other EDC systems preferred.

Experience with reporting tools (e.g. TOAD, Discoverer, Crystal Reports, Clindex Reports, etc.) 

Comply with written procedures, instructions, SOPs and other documents

NormLab2 Plus or other lab normal processing systems experience preferred

Excellent organizational skills and attention to detail


Additional Information

If interested please contact:

Jeff Demaala

973-606-3249

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