Hiring.Camp

Regulatory Assistant

Uchicago

·

Yesterday

Apply
Salary
$19 – $26
Location
Goldblatt Pavilion, United States of America
Workplace
Onsite
Type
Full-time
Department
Legal
Seniority
Entry
Education
Certification
Closing date
Today
Source
Workday

Description

Department

BSD CCC - Clinical Trials Office


About the Department

The University of Chicago Comprehensive Cancer Center (UCCCC) is an integral component of the Biological Sciences Division (BSD). The BSD is the largest of four Divisions of the University and includes the Pritzker School of Medicine. UCCCC administers four established scientific programs, and the NCI-sponsored Cancer Center Support Grant funds ten Shared Resources. The Comprehensive Cancer Center comprises over 190 faculty members from twenty departments, with members currently being awarded over $47 million in total direct costs in peer-reviewed cancer research grants, and $28 million in non-peer-reviewed grants and contracts. The activities of the Center are broad and varied, including research, training and education, communications, fundraising, marketing, clinical trials management, and community outreach.

UCCCC has one of the largest cancer clinical trials programs in the country and in the Chicago area, with nearly 500 adult and pediatric therapeutic trials actively accruing patients. Many of these studies are investigator-initiated, including Phase I or I/II trials, demonstrating UCCCC's commitment to translating basic research findings to the clinic through proof-of-principle and early-phase studies. UCCCC opens over 250 new trials each year and accrues approximately 900 participants to therapeutic trials each year.


Job Summary

The Regulatory Assistant sits within the University of Chicago Medicine Comprehensive Cancer Center (UCCCC) Clinical Trials Support Office (CTSO). The CTSO is organized into eight teams – biobanking, finance, informatics, network operations, study operations/data management, regulatory, training and education, and quality unit/investigator support.

This position serves as an essential support role dedicated to the CTSO regulatory team and provides administrative and business support to ensure compliance with clinical research regulations and guidance documents, internal policies, and National Cancer Institute (NCI) reporting requirements. The Regulatory Assistant is responsible for tracking and distribution of safety updates related to ongoing clinical trials conducted at the UCCCC. This will include collecting these updates from sponsor databases, portals, emails, or other secure methods of distribution, logging events in internal trackers, filing reports in electronic site files, and distributing reports for appropriate internal stakeholder reviews. The position will also support maintenance of essential documents required to support clinical research conduct including maintaining training documentation and relevant licensure, registering clinical research studies in national databases, accrual reporting, and other essential data entry tasks. The Regulatory Assistant will also support other administrative tasks such as supply ordering, meeting scheduling, and document archiving.

This entry-level role requires practical administrative and organizational skills, attention to detail, and the ability to manage multiple concurrent tasks in a fast-paced research environment. The incumbent receives guidance and direction from leadership and senior team members, with the expectation of growing into an independent contributor.

Responsibilities


  • Collects, tracks, and distributes essential safety updates to internal stakeholders.  Maintains accurate records of report receipt and review in internal files to document compliance with internal policies and federal guidance.
  • Assists with data entry and clean-up in the institutional Clinical Trials Management System (CTMS).
  • Registers new clinical research projects in national databases and maintains and updates these study records according to federal and NCI requirements.
  • Enters clinical research accrual data in NCI or related systems. Liases with internal and external stakeholders and study teams to ensure accurate accrual reporting.
  • Maintains and updates site, investigator and staff research credentials (training, licensure, and related items) in investigator site files.
  • Provides administrative support to regulatory team including supply ordering, meeting scheduling, drafting meeting minutes, and documenting archiving.
  • Utilizes analytical thinking, attention to detail, and problem-solving skills.
  • Assists with department or clinic compliance with a high level of guidance.
  • Helps prepare, completes and submits all compliance documentation on a routine basis. Coordinates compliance committee meetings.
  • Performs other related work as needed.


Minimum Qualifications

Education:

Minimum requirements include vocational training, apprenticeships or the equivalent experience in related field (not typically required to have a four-year degree).


Work Experience:

Minimum requirements include knowledge and skills developed through < 2 years of work experience in a related job discipline.


Certifications:

---

Preferred Qualifications


Experience:


  • Prior work experience within office environment.
  • Prior data entry experience.

Preferred Competencies


  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and Adobe Acrobat.
  • Ability to communicate effectively in written and oral formats.
  • Ability to develop proficiency with new software and tools as needed.
  • Strong attention to detail and organizational skills with the ability to multitask and meet deadlines in a fast-paced work environment. 
  • Strong interpersonal skills and ability to interact by phone, email, online meetings or in person with faculty and administrative staff at the University and occasionally with staff of federal government and other institutions and organizations.

Application Documents


  • Resume/CV (required)
  • Cover Letter (preferred)


The University of Chicago uses AI-assisted tools to streamline and augment some recruitment processes; however, AI is not used to make hiring decisions.

When applying, the document(s) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.


Job Family

Legal & Regulatory Affairs


Role Impact

Individual Contributor


Scheduled Weekly Hours

40


Drug Test Required

No


Health Screen Required

No


Motor Vehicle Record Inquiry Required

No


Pay Rate Type

Hourly

​
FLSA Status

Non-Exempt

​
Pay Range

$19.23 - $26.44

The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting.


Benefits Eligible

Yes

The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the Benefits Guidebook.


Posting Statement

The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, shared ancestry, age, status as an individual with a disability, military or veteran status, genetic information, or other protected classes under the law. For additional information please see the University's Notice of Nondiscrimination.

 

Job seekers in need of a reasonable accommodation to complete the application process should call 773-702-5800 or submit a request via Applicant Inquiry Form.

 

All offers of employment are contingent upon a background check that includes a review of conviction history.  A conviction does not automatically preclude University employment.  Rather, the University considers conviction information on a case-by-case basis and assesses the nature of the offense, the circumstances surrounding it, the proximity in time of the conviction, and its relevance to the position.

 

The University of Chicago's Annual Security & Fire Safety Report (Report) provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information. The Report can be accessed online at: http://securityreport.uchicago.edu. Paper copies of the Report are available, upon request, from the University of Chicago Police Department, 850 E. 61st Street, Chicago, IL 60637.

Skills

ExcelClinical TrialsCompliance

Similar Jobs

30

Regulatory Assistant

Fred Hutch·Seattle, Washington

1w ago

Regulatory Assistant

DHC USA·Mechanicsburg, Pennsylvania

3mo ago

REGULATORY ASSISTANT

Qsourcing·Nairobi, Nairobi County

1y+ ago

Executive Assistant, Regulatory Affairs

BeOne·Basel, Basel-City·Onsite

4d ago

Executive Assistant, Regulatory Office

Sunlife·Canada·Hybrid

6d ago

Executive Assistant, Regulatory Office

Sunlife·Canada·Hybrid

6d ago

Clinical Study and Regulatory Assistant

University Health Network·Toronto, Ontario·Onsite

6d ago

Clinical Study and Regulatory Assistant

University Health Network·Toronto, Ontario·Remote, Onsite

6d ago

Food Regulatory Assistant Supervisor

Gardenia Bakeries Philippines Inc·Biñan, Calabarzon·Onsite

2w ago

Legal Assistant, Regulatory

WeirFoulds LLP·Toronto, Ontario·Hybrid

3w ago

Assistant Regulatory Affairs Manager

Estée Lauder Companies·Ho Chi Minh City, Vietnam

1mo ago

Crime & Regulatory Assistant Lawyer

Davies·London, England

1mo ago

UNIV - Clinical Research Assistant (Regulatory) - Department of Medicine: Division of Pulmonary

Career Search·Charleston, South Carolina·Onsite

1mo ago

Assistant Regulatory Affairs Manager

Estée Lauder Companies·Ho Chi Minh City, Vietnam

2mo ago

Research Regulatory Assistant

Brownhealth·Rhode Island, US

3mo ago

Crime & Regulatory - Assistant Lawyer

Davies·Leeds, England

6mo ago

Assistant Manager - Regulatory Compliance (12 month FTC)

IQ-EQ·Douglas, Munster·Hybrid

1d ago

Executive Assistant International; Regulatory Affairs

Takeda·CHE - Glattpark - Zurich HQ, Switzerland·Onsite

2d ago

Assistant Director, Regulatory Compliance

Triplepointllp·London, England

1w ago

Assistant Manager, Regulatory Affairs

Amneal Pharma·Mumbai, Maharashtra·Onsite

2w ago

Executive Assistant, Quality Regulatory and Medical Writing

Neurocrine·US·Onsite

2w ago

Assistant Manager -Regulatory Affairs

Abbott·India > Mumbai : BKC Building

3w ago

Regulatory Reporting, Assistant Vice President

Statestreet·Mumbai, Maharashtra

4w ago

Assistant Manager– Regulatory Affairs

Abbott·India > Mumbai : BKC Building

1mo ago

Assistant Manager - Regulatory & Commercial

Adani·Ahmedabad, Gujarat

1mo ago

Assistant Manager, Regulatory Affairs

Amneal Pharma·India·Onsite

2mo ago

JB-1701 - Assistant Manager - Regulatory Affairs

Rplglobal·Dehradun, Uttarakhand·Remote

2mo ago

Senior Client Delivery Specialist (Energy Regulatory Legal Assistant)

Husch Blackwell·Austin, Texas

2mo ago

Assistant Manager – Regulatory Reporting.Central Account (UAE National Only)

Mashreq·United Arab Emirates·Onsite

2mo ago

Audit and Regulatory Reporting - Assistant Vice President

Icapitalnetwork·Salt Lake City, Utah

2mo ago