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Weekend Clinical Research Regulatory Jobs (NOW HIRING)

Research Regulatory Coordinator

Urbana, IL · On-site

$24.50 - $32.50/hr

Overview The Clinical Research Regulatory Coordinator is a specialized research professional that facilitates and coordinates the regulatory aspects of a clinical trial and plays a critical role in ...

Research Regulatory Coordinator

Urbana, IL · On-site

$25.81 - $43.10/hr

Overview The Clinical Research Regulatory Coordinator is a specialized research professional that facilitates and coordinates the regulatory aspects of a clinical trial and plays a critical role in ...

The University of Alabama at Birmingham (UAB), Department of Med - Pulmonary/Allergy/Critical Care, is seeking a Clinical Research Regulatory Coordinator I. This job position is for an entry-level ...

The Research Regulatory Coordinator manages compliance, documentation, and submissions for clinical ... This role acts as the primary liaison between clinical investigators, institutional review boards ...

Showing results 41-60

Weekend Clinical Research Regulatory information

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$18

$44

$62

How much do weekend clinical research regulatory jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for weekend clinical research regulatory in the United States is $44.13, according to ZipRecruiter salary data. Most workers in this role earn between $36.30 and $52.40 per hour, depending on experience, location, and employer.

What is a Weekend Clinical Research Regulatory professional?

A Weekend Clinical Research Regulatory professional is responsible for ensuring that clinical research studies comply with all regulatory requirements, specifically during weekend shifts. Their duties include preparing and submitting regulatory documents, maintaining ethical standards, and communicating with regulatory agencies and institutional review boards. They play a crucial role in supporting research teams by facilitating timely approvals and monitoring compliance, allowing research activities to continue smoothly over the weekend.

What are the key skills and qualifications needed to thrive as a Weekend Clinical Research Regulatory professional?

To thrive as a Weekend Clinical Research Regulatory professional, you need a solid understanding of clinical research protocols, regulatory guidelines (such as FDA and ICH-GCP), and often a degree in life sciences or a related field. Familiarity with electronic regulatory systems, IRB submission platforms, and certification like CCRC or ACRP is typically required. Excellent attention to detail, strong organizational skills, and effective written communication make someone stand out in this position. These skills ensure that all research activities comply with regulations, maintain data integrity, and support the smooth operation of clinical trials.

What are some common challenges faced by Weekend Clinical Research Regulatory professionals, and how can they be managed?

Weekend Clinical Research Regulatory professionals often face challenges related to limited access to stakeholders and timely responses, as many team members and institutional review boards may not be available outside standard business hours. Managing regulatory documents and ensuring compliance within tight weekend deadlines can also be demanding. Effective planning, clear communication with the weekday team, and utilizing digital tools for document management can help overcome these hurdles. Building strong relationships with colleagues and maintaining detailed handover notes are essential strategies for success in this role.

What is the difference between Weekend Clinical Research Regulatory vs Weekend Clinical Research Coordinator?

AspectWeekend Clinical Research RegulatoryWeekend Clinical Research Coordinator
CertificationsRegulatory Affairs Certification (RAC), Clinical Research CertificationsCPR, Clinical Research Certification
Work EnvironmentRegulatory agencies, compliance departments, sponsor officesResearch sites, hospitals, clinics
Job FocusEnsuring regulatory compliance, preparing submissionsParticipant recruitment, data collection, site coordination

Weekend Clinical Research Regulatory professionals focus on regulatory compliance and submissions, working mainly in offices or regulatory agencies. In contrast, Weekend Clinical Research Coordinators handle participant interactions and data collection at research sites. Both roles require clinical research certifications but differ in daily tasks and work settings.

What cities are hiring for Weekend Clinical Research Regulatory jobs?

Cities with the most Weekend Clinical Research Regulatory job openings:

What are the most commonly searched types of Clinical Research Regulatory jobs?

The most popular types of Clinical Research Regulatory jobs are:

What states have the most Weekend Clinical Research Regulatory jobs?

States with the most job openings for Weekend Clinical Research Regulatory jobs include:

Research Regulatory Coordinator

Carle Health

Urbana, IL • On-site

$24.50 - $32.50/hr

Full-time

Posted 23 days ago


Carle Health rating

7.5

Company rating: 7.5 out of 10

Based on 213 frontline employees who took The Breakroom Quiz

237th of 891 rated healthcare providers


Job description

Overview
The Clinical Research Regulatory Coordinator is a specialized research professional that facilitates and coordinates the regulatory aspects of a clinical trial and plays a critical role in the conduct of research at Carle. This role is responsible for preparing, completing, and submitting required forms and documents, in consultation with the research team, to meet regulatory, IRB, and HIPAA guidelines and policies, at the time of initial review, modifications, and continuing review. The Clinical Research Regulatory Coordinator performs Informed Consent review and modifies consent form/HIPAA language while working with sponsors and IRBs for all studies to conform to Carle institutional guidelines.
Qualifications
Certifications: Certified Clinical Research Professional (CCRP) within 3 years - Society of Clinical Research Associates (SOCRA)Society of Clinical Research Associates (SOCRA), Education: Experience In Lieu of Education: Related Field; Bachelor's Degree: Related Field, Work Experience: Related field
Responsibilities
Prepares, completes, and submits required forms and documents, in consultation with the research team, to meet regulatory, IRB, and HIPAA guidelines and policies, at the time of initial review, modifications, and continuing review. Performs Informed Consent review and modifies consent form/HIPAA language while working with sponsors and IRBs for all studies to conform to Carle institutional guidelines. Ensures consent language matches the research contract, budget, and protocol. Completes, submits, and maintains regulatory documents as applicable (including 1572s, Delegation of Authority logs, Financial Disclosure Forms, Consent Forms, and trainings) for industry sponsored as required. Prepares for and participates in external sponsor/monitor visits. Prepares for and participates in internal/external audits to ensure regulatory compliance and implement corrective and preventive action plans as needed. Updates and maintains current protocol information on the Research website. Distributes protocol documents to appropriate researcher and PI for review, approval, and implementation. Tracks study approvals and expirations to ensure uninterrupted project approval. Maintains regulatory database and manages electronic filing of all regulatory documents. Creates, submits, and maintains complete documentation to comply with research base regulatory requirements for oncology federally funded research projects Trains/assists new/seasoned Staff on regulatory process including CITI training, Study start-up, IRB submissions, maintaining a Study, and ensuring all essential documents are correct to submit to monitor/sponsor. Advises on remedies and revisions, in collaboration with the coordinator and/or investigator, and resolves any procedural issues that might arise in order to ensure timely IRB review Updates and maintains the active informed consent documents and HIPAA authorizations that are being utilized in projects in which subjects are consented (whether Carle research is assisting with consenting or not) Notifies appropriate staff, physicians, investigators and affiliates of protocol activations and closures in a timely manner Facilitates study closure in collaboration with investigator, research coordinator, and sponsor Applies rules and regulations (Carle local, state, federal, industry, sponsor, etc.), in collaboration with the Sr Clinical Research Regulatory Coordinator, and recommends and guides principal investigators (PIs) and research staff in the creation, submission, documenting, reporting, etc. of study activities ensuring appropriate compliance Monitors Investigator Initiated IRB-deferred studies, exempt and non-engaged projects for by ensuring regulatory documentation is current and maintained , including any IRB approvals
About Us
Find it here.
Discover the job, the career, the purpose you were meant for. At Carle Health, we're committed to fostering a workplace where every team member feels valued, respected and empowered, where passion and purpose come together to positively impact the lives of our patients and our communities. Find it all at Carle Health.
Our nearly 17,000 team members and providers work together to support patient care across central and southeastern Illinois. We've grown to include eight, award-winning hospitals and a multispecialty provider group with more than 1,500 doctors and advanced practice providers. We're developing the next generation of providers and healthcare professionals through Carle Illinois College of Medicine, the world's first engineering-based medical school, and Methodist College. Carle BroMenn Medical Center, Carle Foundation Hospital, Carle Health Methodist Hospital, Carle Health Proctor Hospital, Carle Health Pekin Hospital, and Carle Hoopeston Regional Health Center hold Magnet® designations, the nation's highest honor for nursing care. We offer opportunities in several communities throughout central Illinois with potential for growth and life-long careers at Carle Health.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. Carle Health participates in E-Verify and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization. | For more information: human.resources@carle.com.
Compensation and Benefits
The compensation range for this position is $25.81per hour - $43.1per hour. This represents a good faith minimum and maximum range for the role at the time of posting by Carle Health. The actual compensation offered a candidate will be dependent on a variety of factors including, but not limited to, the candidate's experience, qualifications, location, training, licenses, shifts worked and compensation model. Carle Health offers a comprehensive benefits package for team members and providers. To learn more visit careers.carlehealth.org/benefits.

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About Carle

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Each and every employee at Carle makes us better and stronger, so we can take care of our patients and our community. From clinical to professional and technical careers – our team of employees help us change lives. Carle is proud to be named a Great Place to Work®. Alongside Carle BroMenn Medical Center, Carle Health Methodist Hospital, and Carle Health Proctor Hospital, the Carle Foundation Hospital holds Magnet® designation, the nation’s highest honor for nursing care.

Industry

Health care and social assistance, hospitals and outpatient health care

Company size

10,000+ Employees

Headquarters location

Urbana, IL, US