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Weekend Irb Jobs in Riverside, CA (NOW HIRING)

Red Hawk Services

Be Seen First

Lead Automated Gate Installer

Perris, CA · On-site

$34 - $50/hr

... Omron,IRB RET, Secolarm etc.) or the like - Perform saw cutting inductive loops - Perform ... Weekends as needed

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 ...

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.

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 ...

Pinnacle Clinical Research

Physician

Riverside, CA · On-site

It is conducted in accordance with the IRB-approved plan * That they will ensure the accuracy ... Provides some weekend coverage to facilitate study visits per protocol. * Provides after-hours ...

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

$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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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

Clinical Research Coordinator

Pomona, CA • On-site

ECN Operating LLC
See more jobs at ECN Operating LLCexternal

$24 - $28/hr

Full-time

Posted 3 days ago

New

Job description

Job Summary:

We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.

Key Responsibilities:

  • Coordinate day-to-day clinical research activities to ensure study protocols are followed.
  • Recruit, screen, and enroll study participants.
  • Obtain informed consent and ensure ethical conduct in all study interactions.
  • Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples).
  • Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs).
  • Maintain accurate and timely documentation in case report forms and electronic databases.
  • Communicate with sponsors, monitors, and IRBs regarding study progress and compliance.
  • Schedule participant visits and follow-ups; ensure visit windows are met.
  • Ensure proper storage, handling, and accountability of investigational products, if applicable.
  • Maintain regulatory documents and assist with IRB submissions.

Qualifications:

  • Bachelor's degree in a health-related field required.
  • At least 1–2 years of experience in clinical research preferred.
  • Phlebotomy certification or MA certification preferred.
  • Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
  • Excellent organizational skills and attention to detail.
  • Strong interpersonal and communication skills.
  • Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms).
  • Ability to work independently and as part of a multidisciplinary team.

Preferred Qualifications:

  • Experience working in clinical trials, especially in a hospital or academic setting.
  • Familiarity with IRB processes and clinical trial documentation.
  • Bilingual skills (depending on patient population) may be a plus.

Job Type: Full-time

Work Location: In person

Schedule:

  • 8 hour shift
  • Monday to Friday
  • Weekends as needed

Pay

  • $24 - $28 per hour