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Regulatory Affairs Associate

Job

Randstad USA

North Chicago, IL (In Person)

$62,701 Salary, Full-Time

Posted 5 days ago (Updated 1 day ago) • Actively hiring

Expires 7/19/2026

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Job Description

job summary: Are you a recent life sciences graduate looking to launch your career with a Top-Tier Global Pharma Leader? This hybrid Regulatory Affairs Associate I role in North Chicago, IL, offers an incredible opportunity to gain hands-on experience in regulatory information management, working with advanced industry systems in a collaborative, fast-paced environment.
Duration:
1-
Year ContractLocation:
North Chicago, IL (
Hybrid:
Onsite Tuesday, Wednesday, Thursday)
Interview Process:
1-2 sequential virtual panel interviews location: North Chicago, Illinois job type: Contract salary: $28.00 - 32.29 per hour work hours: 9 to 5 education: Bachelors responsibilities: Support regional regulatory information management (RIM) activities, focusing on key data systems and processes. Partner with the central data management team to create market-specific RIM objects following strict data standards. Create and update product registrations to align with new approvals, renewals, indications, or pack changes. Track, record, and update regulatory commitments, obligations, submissions, and agency correspondences. Monitor tracking systems to ensure submission and approval dates are accurately recorded and archived. Collaborate on monthly quality control reports, identifying data gaps and supporting remediation activities.
qualifications:
Bachelor's degree in a related life science field (Pharmacy, Biology, Chemistry, Medical Technology, or Pharmacology) Recent graduate with a Pharmacy or Health Sciences background Strong oral and written communication skills Ability to work onsite in North Chicago, IL, 3 days per week (Tuesday-Thursday) #LI-AO1 skills:
Regulatory Affairs Operations, Regulatory Submission Compliance Equal Opportunity Employer:
Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. job detailssummary$28 - $32.29 per hourcontractbachelor degreecategorylife, physical, and social science occupationsreference53848job details job summary: Are you a recent life sciences graduate looking to launch your career with a Top-Tier Global Pharma Leader? This hybrid Regulatory Affairs Associate I role in North Chicago, IL, offers an incredible opportunity to gain hands-on experience in regulatory information management, working with advanced industry systems in a collaborative, fast-paced environment.
Duration:
1-
Year ContractLocation:
North Chicago, IL (
Hybrid:
Onsite Tuesday, Wednesday, Thursday)
Interview Process:
1-2 sequential virtual panel interviews location: North Chicago, Illinois job type: Contract salary: $28.00 - 32.29 per hour work hours: 9 to 5 education: Bachelors responsibilities: Support regional regulatory information management (RIM) activities, focusing on key data systems and processes. Partner with the central data management team to create market-specific RIM objects following strict data standards. Create and update product registrations to align with new approvals, renewals, indications, or pack changes. Track, record, and update regulatory commitments, obligations, submissions, and agency correspondences. Monitor tracking systems to ensure submission and approval dates are accurately recorded and archived. Collaborate on monthly quality control reports, identifying data gaps and supporting remediation activities.
qualifications:
Bachelor's degree in a related life science field (Pharmacy, Biology, Chemistry, Medical Technology, or Pharmacology) Recent graduate with a Pharmacy or Health Sciences background Strong oral and written communication skills Ability to work onsite in North Chicago, IL, 3 days per week (Tuesday-Thursday) #LI-AO1 skills:
Regulatory Affairs Operations, Regulatory Submission Compliance Equal Opportunity Employer:
Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.