Team Lead of Site Operations (Oncology) Zp Group LlcTeam Lead of Site Operations (Oncology)Downers Grove, IL$80,000–$90,000 / yearThe Team Lead, Site Operations (Oncology) role is ideal for an experienced oncology research professional with leadership experience supporting high-quality site operations across multiple clinical studies. Keywords: Team Lead, Site Operations, Oncology Clinical Research, Clinical Trials, Clinical Research Coordinator, Clinical Research Nurse, GCP, Site Management, Clinical Operations, Oncology Studies.
CRC Level 1 ICON PlcCRC Level 1Downers Grove, IL$42,600–$53,250 / yearWhat you will be doing: Performing technical and clinical requirements of study protocols, i.e., venipuncture, specimen processing, vital signs, electrocardiograms, IV infusions, IV pump operations, Holtor monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, injections (IM or SQ) or any procedure necessary for the protocol as ordered by the investigator. Obtaining and maintaining knowledge in regards to temperature monitoring devices and procedures for lab specimens and investigational products and providing detailed information to all staff and sponsors in regards to how temperatures are monitored and maintained.
Embedded Patient Engagement Specialist (Munster, IN) Profound Research LLCEmbedded Patient Engagement Specialist (Munster, IN)Munster, INWhy this Role Exists: The Embedded Patient Recruitment Specialist should exhibit a platinum level of customer service, acknowledging and greeting patients with a smile, eager to answer questions and exhibiting an unparalleled attention to detail, while maintaining thorough data records. The Embedded Patient Recruitment Specialist is involved with all aspects of patient recruitment from initiating advertising, chart screening, through initial patient contact to scheduling for first visits or follow up visits.
Regulatory Coordinator-Genetics Ann & Robert H. Lurie Children's Hospital of ChicagoRegulatory Coordinator-GeneticsChicago, Illinois$65,520–$107,120 / yearGuides and coordinates all clinical trials-related submissions, documentation, and reporting processes (new study applications, renewals, revisions, modifications, amendments, adverse events, safety reports, close-out, etc.) recommending alternatives to ensure compliance and approval. Acts as a liaison between affiliate institutions, study sponsors, study coordinators, investigators, and appropriate oversight/regulatory agencies when questions, issues, problems arise regarding study status and process.
Embedded Patient Engagement Specialist (Munster, IN) Profound ResearchEmbedded Patient Engagement Specialist (Munster, IN)Munster, IndianaWhy this Role Exists: The Embedded Patient Recruitment Specialist should exhibit a platinum level of customer service, acknowledging and greeting patients with a smile, eager to answer questions and exhibiting an unparalleled attention to detail, while maintaining thorough data records. Drive enrollment and retention -Interact with potential clinical trial participants to recruit, assess eligibility criteria, determine patient/subject availability, and coordinate appointments -Demonstrate knowledge of clinical research protocols including inclusions/exclusions.
NewEnterprise Account Executive, MedTech Data Solutions HirexHireEnterprise Account Executive, MedTech Data SolutionsChicago, ILFull timeThe ideal candidate will bring deep expertise in real-world evidence, clinical research, and healthcare data, along with an established executive network and a proven track record of selling high-value, consultative solutions. Stay current on clinical research trends, regulatory requirements, HEOR, RWE commercialization, and the broader healthcare data landscape to effectively advise customers and identify new opportunities.
Senior Director, Corporate Strategy - Prolaio KardiganSenior Director, Corporate Strategy - ProlaioChicago, Illinois$240,000–$270,000 / yearThis role focuses on framing Prolaio’s most critical strategic questions; conducting market landscaping, market research, and market sizing; shaping pricing and monetization strategies; developing business cases and financial analyses for new growth opportunities; and driving execution across complex, cross‑functional initiatives. While the role sits within Kardigan’s Corporate Strategy function and reports to the Vice President of Corporate Strategy, it operates day‑to‑day as a dedicated strategic leader for Prolaio, working in close partnership with the Prolaio General Manager and leadership team.
CRC Float Nurse University of ChicagoCRC Float NurseIL$60–$70 / hourReporting directly to the Clinical Research Center Manager, the Clinical Research Center (CRC) Float Nurse participates in a variety of clinical research projects/studies involving various study designs and procedures for participants, including multi‐centered cooperative group and intergroup trials at a national level, multi‐institutional pharmaceutical trials, single and multi‐centered trials, and observational, registry and phenotypical studies, designed, implemented, and coordinated in the CRC. Over its thirteen years, the ITM has capitalized on the outstanding intellectual and physical resources throughout the University and at ITM affiliate Institutions, Argonne National Laboratory, NorthShore University HealthSystem, Illinois Institute of Technology, and Access Community Health Network, and on substantial institutional and CTSA financial investments, to build the infrastructure for a transformative, energized, and self-improving home for clinical and translational research, ensuring the continued progress of clinical and translational science at the University of Chicago, its affiliates, on the South Side of Chicago, and beyond.
Regulatory Coordinator-Genetics Ann & Robert H Lurie Children's Hospital of ChicagoRegulatory Coordinator-GeneticsChicago, IL$65,520–$107,120 / yearGuides and coordinates all clinical trials-related submissions, documentation, and reporting processes (new study applications, renewals, revisions, modifications, amendments, adverse events, safety reports, close-out, etc.) recommending alternatives to ensure compliance and approval. Knowledge, Skills and Abilities: Bachelor's degree or the equivalent and three years of work experience in a regulatory and/or research environment having developed a strong working knowledge of clinical research protocols required.
Senior Director, Corporate Strategy - Prolaio KardiganSenior Director, Corporate Strategy - ProlaioChicago, IllinoisThis role focuses on framing Prolaio’s most critical strategic questions; conducting market landscaping, market research, and market sizing; shaping pricing and monetization strategies; developing business cases and financial analyses for new growth opportunities; and driving execution across complex, cross‑functional initiatives. While the role sits within Kardigan’s Corporate Strategy function and reports to the Vice President of Corporate Strategy, it operates day‑to‑day as a dedicated strategic leader for Prolaio, working in close partnership with the Prolaio General Manager and leadership team.
Oncore Compliance & Monitoring Analyst University of ChicagoOncore Compliance & Monitoring AnalystChicago, IL$65,000–$90,000 / yearThe Office of Clinical Research (OCR) is dedicated to supporting the infrastructure for the management and administration of clinical research at The University of Chicago as well as individual research programs with the goal of improving communication, consistency, and collaboration across the Biological Sciences Division and UChicago Medicine. To mission of the OCR is to catalyze clinical research by providing expertise, resources, infrastructure, and systems that facilitate clinical research operations and enable collaboration across the enterprise while promoting compliance and human subject protection on behalf of our diverse community of patients and volunteers.
Oncore Training Specialist University of ChicagoOncore Training SpecialistChicago, IL$70,000–$100,000 / yearAs a member of the Research Systems & Coverage Analysis (RSCA) Unit within the Office of Clinical Research, the OnCore Training Specialist works as part of a team to support and optimize clinical research operations, partnering closely with research teams and key stakeholders throughout the institution. The Office of Clinical Research (OCR) is dedicated to supporting the infrastructure for the management and administration of clinical research at The University of Chicago as well as individual research programs with the goal of improving communication, consistency, and collaboration across the Biological Sciences Division and UChicago Medicine.
Regulatory Coordinator Ann & Robert H. Lurie Children's Hospital of ChicagoRegulatory CoordinatorChicago, IllinoisGuides and coordinates all clinical trials-related submissions, documentation, and reporting processes (new study applications, renewals, revisions, modifications, amendments, adverse events, safety reports, close-out, etc.) recommending alternatives to ensure compliance and approval. Coordinates and guides the review and approval process of all research activities associated with complicated clinical research studies involving human subjects in the Hematology, Oncology and Stem Cell Transplantation Division, ensuring the protection of their safety, rights, and welfare.
Regulatory Coordinator Northwestern UniversityRegulatory CoordinatorChicago, IL$57,000–$66,734 / yearThe Regulatory Coordinator ensures that all study activities are completed by strictly following Good Clinical Practice (GCP) & all current local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board (IRB), Food and Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH). Our dynamic team is composed of faculty and staff colleagues with expertise in a wide variety of domains, including: clinical research infrastructure (e.g., regulatory, budget/finance), bioinformatics & data science, biostatistics, community-engaged research, education & career development, team science, etc.
Regulatory Coordinator Ann & Robert H Lurie Children's Hospital of ChicagoRegulatory CoordinatorChicago, ILGuides and coordinates all clinical trials-related submissions, documentation, and reporting processes (new study applications, renewals, revisions, modifications, amendments, adverse events, safety reports, close-out, etc.) recommending alternatives to ensure compliance and approval. Coordinates and guides the review and approval process of all research activities associated with complicated clinical research studies involving human subjects in the Hematology, Oncology and Stem Cell Transplantation Division, ensuring the protection of their safety, rights, and welfare.
Dental Assistant University of ChicagoDental AssistantChicago, IL$21.63–$26.44 / hourThe DA1 is an entry level position responsible for chairside assisting to dental providers providing dental care to patients at the University of Chicago Medicine (UCM) Dental Research Study Clinic at its main campus in Hyde Park as well as other study sites, including mobile dental units. Provides services at UCM Dental Research Study Clinic as well as affiliated study sites including mobile dental units across Chicagoland area, including on regular evening and weekend shifts.
Campus/Virtual/Pop-up Lab Manager University of ChicagoCampus/Virtual/Pop-up Lab ManagerChicago, IL$50,000–$58,000 / yearProvides oversight and project management for research conducted in the RFCDR Labs by affiliated faculty and graduate students, overseeing the full life-cycle of each research study from research request submission through final delivery of collected data, across RFCDR Lab sites (Campus Lab, Virtual Lab, and Pop-up Lab locations). Maintains current training in research ethics, including the Collaborative Institutional Training Initiative (CITI Program), and assists in training and overseeing the RF-CDR Labs research assistants as they engage with participants, as well as maintaining documentation of RF-CDR team member's ethics training.
Campus/Virtual/Pop-Up Lab Manager University of ChicagoCampus/Virtual/Pop-Up Lab ManagerChicago, IL$50,000–$58,000 / yearProvides oversight and project management for research conducted in the RFCDR Labs by affiliated faculty and graduate students, overseeing the full life-cycle of each research study from research request submission through final delivery of collected data, across RFCDR Lab sites (Campus Lab, Virtual Lab, and Pop-up Lab locations). Maintains current training in research ethics, including the Collaborative Institutional Training Initiative (CITI Program), and assists in training and overseeing the RF-CDR Labs research assistants as they engage with participants, as well as maintaining documentation of RF-CDR team member's ethics training.
Principal Investigator Flourish ResearchPrincipal InvestigatorChicago, IllinoisRepresent Flourish Research in a professional and courteous manner (verbal, written, and in appearance) during all interactions with sponsors, physicians, physicians' office personnel, participants, Flourish Research employees, Flourish Research contract personnel, as well as any other person(s) when carrying out task and responsibilities. ESSENTIAL JOB FUNCTIONS: · Ensure the maintenance of confidentiality by team members of participant information as appropriate and as bound by Confidentiality Agreements with Flourish Research, between Flourish Research and sponsors/CROs and between Flourish Research and other entities while abiding by HIPAA regulations.
Associate Dean, Corporate Partnerships and Innovation Northwestern UniversityAssociate Dean, Corporate Partnerships and InnovationChicago, IL$174,928–$228,646 / yearJob Summary: The Associate Dean, Corporate Partnerships and Innovation provides executive-level leadership for the Northwestern University Feinberg School of Medicine (FSM) corporate engagement enterprise, including industry-funded research and clinical trials, and supports research innovation and commercialization pathways through a partnership with the Innovation and New Ventures Office (INVO). The person in this role sets strategic vision and long‑term partnership direction for the medical school, and collaborates with NU Sponsored Research, Corporate Engagement, NUCATS, and clinical research operations to develop integrated, high‑impact partnerships.