Regulatory Affairs Lead - Clinical Research
Lurie Children's Hospital
Ann & Robert H. Lurie Children’s Hospital of Chicago seeks a Regulatory/Research Compliance professional to oversee complex clinical studies involving human subjects in hematology, oncology and stem cell transplantation. You will interpret regulations, coordinate IRB submissions, and guide investigators and staff to maintain safety, rights, and welfare. You’ll liaise with affiliates, sponsors, and regulatory agencies, develop compliant documentation, and train teams to uphold rigorous ethical #J-18808-Ljbffr Lurie Children's Hospital
- ...within the Biological Sciences Division is seeking a Regulatory Compliance Officer to manage trial regulatory programs... ...interfaces with IRB and sponsor agencies. Minimum 2-5 years in clinical research or regulatory affairs, with a degree in a related field. #J-18808-Ljbffr...Suggested
- ...quest for better?Job DescriptionThe Lead Advanced Practice Provider (APP)- Interventional... ...procedures, guidelines and all other regulatory and accreditation standards.The Lead... ...care decision-making through expert clinical reasoning, research and theory-based practice. This role...SuggestedFull timeWork at officeLocal areaRelocation packageMonday to FridayWeekend work
- A clinical research organization in Chicago is seeking an experienced audit support professional. The role involves facilitating the audit request process for regulatory inspections, conducting data analytics, and implementing process improvements. Candidates should have...Suggested
$88.6k - $246.6k
The Solution Implementation Lead is the end‑to‑end execution owner... ...supporting respiratory clinical trials (e.g., asthma, COPD, pulmonary... ..., operational workflows, regulatory considerations, and... ...global provider of clinical research services, commercial insights...SuggestedFull timePart timeImmediate startRemote workWorldwide- The University of Chicago invites applications for the Clinical Research Manager in Hematology/Oncology. You will oversee project management, data management and clinical monitoring across sponsored, grant funded and multi-site trials, coordinating with sites, the Clinical...SuggestedWork at office
- Northwestern University is seeking a research project manager within MED-Rheumatology in Chicago to lead daily operations of biomedical or social-behavioral studies... ...ensure protocol quality, GCP compliance, and regulatory alignment. The role involves data analysis, grant...
- AbbVie is seeking a Senior Associate in Regulatory Affairs Submission Management. This role manages medium to high impact submission projects, coordinating cross-functional teams to ensure timely, compliant dossiers for regulatory authorities. The position emphasizes acting...
- Lesaffre, including its Gnosis by Lesaffre division, seeks a Manager of Regulatory Affairs to lead the Americas regulatory strategy, ensuring US and Canadian market access and compliant labeling practices. The role partners with global teams to align regulatory efforts...
$265k - $290k
...transformational change for the world’s leading brands. With more than 1,400 employees across... ...for centralizing and governing all regulatory, environmental, safety, and client/brand... ...compliance and advocacy) Legal / Regulatory Affairs (interpretation of laws and standards)...Shift work- Barrington James is seeking a Senior Clinical Research Associate for a small CRO focused on US-based studies. The role involves independently performing site selection, initiation, routine monitoring, and close-out visits in accordance with protocol and ICH-GCP guidelines...
$60k - $85k
The Biological Sciences Division at the University of Chicago is hiring a Protocol Coordinator to manage protocol development and implementation. This role requires a college degree and 2–5 years of related experience. Responsibilities include liaising with funding agencies...$36.06 - $40.87 per hour
...Loyola University Chicago is hiring a Clinical Research Nurse in Maywood, Illinois. This role involves planning clinical trials, overseeing patient enrollment, and ensuring protocol compliance. Candidates must possess a Bachelor's Degree in Nursing and have 1-2 years of...Hourly pay- ...together to generate business value from clinical trials data. Our operational model is exemplified... ...-level strategies. For assigned studies, leads the CDSO Study Team and represents DS as... ...have at 3+ years of pharma / clinical research / data management / health care...Contract workTemporary workWork experience placementLocal area
- ...Endeavor Health's Evanston Hospital seeks a Research Coordinator- Anesthesia to support the development of a sustainable research program. You will assist with IRB protocol development, recruit and consent patients, and maintain precise study records while collaborating...
$174.1k - $287.27k
Job DescriptionAre You Ready to Make It Happen at Mondelēz International?Join our Mission to Lead the Future of Snacking. Make It Uniquely Yours.:Supply Chain Excellence/IL6S Program Leadership, Governance and ExecutionDevelop and globally deploy the IL6S framework, methodologies...Full timeRelocation package$98k - $110k
...Assistant Vice President - Funding & Settlements, the Process Lead will oversee critical functions within the team, including the... ...Accurately reviews and approves transactions, ensuring compliance with regulatory standards and company policies.Problem Solving: Acts swiftly as...Full timeTemporary workWork at officeShift work- ...Labeling Strategy at a glance….The Group Lead, Food Regulation & Labeling Strategy provides... ...& Strategy team, with accountability for regulatory oversight and direction across... ...product development, nutrition, scientific affairs, or quality Strong knowledge of FDA and/or...Full timeFlexible hours
- ...C3 Generative AI, a suite of domain-specific generative AI offerings for the enterprise. Learn more at: C3 AIForward Deployed Team Leads are senior technical leads who own a commercial or enterprise customer end-to-end. You’ll combine strong technical architecture, hands...
$125k - $150k
...FullscriptWe’re an industry-leading health technology company on... ...practitioners use Fullscript for clinical insights, lab interpretations... ...AI, product development, and regulatory compliance, partnering... ...checkpoints. Support clinical research, outcomes tracking, and de-identification...Full time$230k - $280k
...eligible Clinician-Educator at the rank of Assistant Professor in Allergy and Immunology. Responsibilities include advancing clinical and research missions while attending clinics and participating in educational activities. Candidates must have a strong background in...Full time- ...infection control in Oak Lawn, Illinois. The incumbent will perform surveillance for infections, provide education, and contribute to clinical research. A Bachelor’s Degree in Nursing or related field, an RN license, and 5 years of clinical experience are required. This...
- Vienna Beef is seeking a Supervisor to oversee pickle production, ensuring compliance with FDA and FSIS directives, customer orders, and company specs. The role focuses on optimizing labor, equipment and materials to meet tonnage goals while maintaining quality and safety...
$65k - $80k
...Lead Clinical Research Data Manager The Section of Hematology/Oncology has a proud and long tradition of excellence in research-based patient... ...formulas, generating automated reports, and preparing regulatory-compliant documents. Familiarity with common electronic...Work experience placement- ...Lurie Children’s Hospital of Chicago is seeking a qualified clinical research professional to coordinate all aspects of pediatric studies... ...minimal supervision. The role involves managing study start-up, regulatory submissions, data handling, participant enrollment, and...
- ...University of Chicago's BSD MED - Hematology and Oncology - Clinical Research team seeks a Clinical Research Manager to oversee multiple trials... ...data collection, monitor adherence to protocols, and ensure regulatory compliance. You will liaise with clinical sites, sponsors,...Work at office
$26 per hour
...what you do, you’re going to want to be here.Join us and become part of the power behind possible.**About The Opportunity**The Floor Lead ensures an acceptable finished product for our customer. The person in this position is responsible for overseeing of the production...Hourly payTemporary workWork at officeShift workRotating shiftWeekend work- University of Illinois Chicago is seeking a Senior Clinical Research Coordinator in the Neurology and Rehabilitation department. The role... ...and timelines. Responsibilities include protocol activation, regulatory submissions, and collaboration with the PI, sponsors, and IRB...
- Rush University Medical Center in Chicago is hiring a Clinical Research Coordinator III to manage clinical trials. The role entails ensuring compliance, coordinating communication, and resolving operational challenges with minimal oversight. The ideal candidate will have...Full time
$167k - $260k
...at wellsfargojobs.com.About this role:Wells Fargo is seeking a Lead Treasury Management Consultant within Global Payments & Liquidity... ...risk programs (Credit, Market, Financial Crimes, Operational, Regulatory Compliance), which includes effectively following and adhering...Full timeWork experience placement- ...Responsibilities: Facilitate audit request process for GxP regulatory inspections, customer audits, and internal quality audits. Develop a strong understanding of SLC and system evidence to support audits. Leverage available resources and improve resources...
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