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Weekend Irb Jobs in Riverside, CA (NOW HIRING)

JenaValve

Senior Associate, Clinical Research

Irvine, CA · On-site

$95K/yr

IRB continuing review approval period and expiration dates). * Provide clinical operational support during preparation for and conduct of all clinical audits and inspections. * Contribute to the ...

Synectics

Physician

Riverside, CA · On-site

Ensuring studies follow the IRB-approved protocol. * Maintaining the accuracy, security, and ... Provide occasional weekend coverage to facilitate study visits according to protocol requirements.

New

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

Clinical Trial Administration * Assist with trial start-up, including preparing and submitting regulatory and ethics documents, such as IRB/EC submissions, contracts, and site feasibility ...

Diality Inc

Clinical Research Associate

Irvine, CA · On-site

$120K - $135K/yr

Clinical Trial Administration * Assist with trial start-up, including preparing and submitting regulatory and ethics documents, such as IRB/EC submissions, contracts, and site feasibility ...

Medix

Clinical Research Coordinator

Murrieta, CA · On-site

$31 - $38/hr

Obtain informed consent per federal regs, GCP, and IRB requirements. * Ethically recruit qualified ... Monday-Friday, 8:30 AM - 5 PM (occasional weekends) * We will consider for employment all qualified ...

Flourish Research

Research Assistant

Murrieta, CA · On-site

$21 - $32/hr

Monday-Friday, 8:30 AM - 5 PM (occasional weekends) Location: Murrieta, CA Compensation: $21 - $32 ... Obtain and document informed consent following federal regulations and IRB guidelines * Support ...

Flourish Research

Research Assistant

Murrieta, CA · On-site

$21 - $32/hr

Monday-Friday, 8:30 AM - 5 PM (occasional weekends) Location: Murrieta, CA Compensation: $21 - $32 ... Obtain and document informed consent following federal regulations and IRB guidelines * Support ...

Flourish Research

Research Assistant

Murrieta, CA · On-site

$21 - $32/hr

Monday-Friday, 8:30 AM - 5 PM (occasional weekends) Location: Murrieta, CA Compensation: $21 - $32 ... Obtain and document informed consent following federal regulations and IRB guidelines * Support ...

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Showing results 1-20

All JobsIrb JobsWeekend Irb JobsWeekend Irb Jobs in Riverside, CA

Weekend Irb information

What is a weekend IRB?

Weekend IRB jobs refer to positions related to Institutional Review Boards (IRBs) that operate or require work during weekends. IRBs are committees established to review and approve research involving human subjects, ensuring ethical standards are met. Weekend IRB staff may include coordinators, administrators, or reviewers who process submissions, review protocols, and ensure compliance outside of normal weekday hours to accommodate researchers' needs and deadlines.

What are the typical responsibilities of a weekend IRB member?

As a Weekend IRB (Institutional Review Board) member, your primary responsibility is to review research protocols submitted for ethical and regulatory compliance, particularly those requiring urgent or expedited consideration over weekends. This role often involves collaborating remotely with fellow board members, principal investigators, and compliance staff to ensure timely feedback on submissions. Challenges may include balancing multiple protocols with tight deadlines and maintaining clear communication despite limited in-person interaction. Your input directly impacts participant safety and institutional compliance, making attention to detail and ethical judgment essential.

What are the key skills and qualifications needed to thrive as a weekend IRB member?

To thrive as an IRB member, you generally need a background in research ethics, regulatory compliance, and relevant academic or clinical experience, often supported by advanced degrees in health, law, or social sciences. Familiarity with federal regulations (such as 45 CFR 46), online protocol management systems, and human subjects protection certifications (e.g., CITI Program) is typically required. Strong analytical thinking, attention to detail, impartiality, and effective communication skills distinguish outstanding IRB members. These skills ensure that research protocols are ethically reviewed, participant rights are protected, and institutional compliance is maintained.

What is the difference between Weekend IRB vs IRB Coordinator?

AspectWeekend IRBIRB Coordinator
CertificationsOften requires IRB-related training, but not always formal certificationsTypically requires IRB or research compliance certifications
Work EnvironmentPart-time, flexible hours, often on weekends or eveningsFull-time, office-based, regular weekday schedule
Employer & IndustryResearch institutions, hospitals, universitiesResearch institutions, hospitals, universities

Weekend IRB roles focus on providing oversight during non-standard hours, often with flexible schedules, while IRB Coordinators handle ongoing compliance, documentation, and communication during regular hours. Both roles are essential in research oversight but differ mainly in work hours and specific responsibilities.

How to get a Weekend IRB job?

To get a Weekend IRB job, candidates should have relevant experience in research or clinical settings, often requiring knowledge of regulatory compliance and ethical review processes. Strong organizational skills and the ability to work independently during weekends are important. Applying through job boards, networking within research institutions, and obtaining certifications like GCP can improve chances.

What cities near Riverside, CA are hiring for Weekend Irb jobs?

Cities near Riverside, CA with the most Weekend Irb job openings:

Weekend Irb jobs near you

Senior Associate, Clinical Research

JENAVALVE TECHNOLOGY INC

Irvine, CA

Full-time

Re-posted 28 days ago

Job description

Job Title: Senior Associate, Clinical Research  

Role Level: Individual Contributor (IC)

Supervisor/Manager Title: Director, Clinical Affairs 

Job Location & Environment: Irvine, CA, Corporate Office

Job Description Summary: The Senior Clinical Research Associate will report to the Director, Clinical Affairs, and will play a key role in proactively supporting the conduct of pre-market clinical studies and ensure compliance with all regulatory requirements. The ideal candidate will have a thorough knowledge of Good Clinical Practices (GCP) and applicable regulations. 

Job Responsibilities: 

  • Support site management and interact with site coordinators, investigators, and field monitors in collecting data and resolving queries to meet the protocol requirements in a timely manner.
  • Ensure quality data management activities – i.e., data review, query generation and resolution. Generate status reports to clinical staff and management.
  • Generate queries to resolve data issues and apply corrections to database.
  • Act as a point person for all data related to clinical group, and to provide data to cross-functional departments.
  • Conduct EDC training to external teams and sites.
  • Maintain Trial Master Files and trackers for clinical trials.
  • Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current.
  • Conduct periodic audits of internal files to ensure compliance per site Institutional Review Board (IRB) and/or Ethics Committee (EC) policy (i.e. IRB continuing review approval period and expiration dates). 
  • Provide clinical operational support during preparation for and conduct of all clinical audits and inspections.
  • Contribute to the development and implementation of departmental policies, standards, and process improvement initiatives. 
  • Partner with management to manage external vendors, including ongoing supplier qualification.
  • Assist field clinical monitors in preparation for site training and monitoring visits
  • Support co-monitoring of local sites on an as-needed basis.

Required Education and Experience: 

  • 2+ year of experience in clinical trial research is required (preferred in medical devices).
  • Advanced degree in a biological science / pharmacy/ nursing desired.

Skills and Abilities Required for This Job: 

  • Proficient in clinical trial management and electronic data capture systems to document and record information.
  • Excellent communication skills (written and verbal English) so as to be able to build effective relationships with trial center staff and colleagues.
  • Deep knowledge of GCPs governing the conduct of clinical trials; working knowledge of Medical Device Directive 93/42/EEC, ISO14155 and ICH guidelines. 
  • Very organized and able to pay close attention to detail.
  • Team player with a willingness to help where needed and work with diverse people.

Physical Requirements: 

  • Ability to travel up to 20% time.

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