Clinical Research Associate (Cra) - Oncology (Remote) Merck & Co., Inc.Clinical Research Associate (Cra) - Oncology (Remote)Chicago, ILRemote$96,200–$151,400 / yearConducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner. Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites.
Oncology Clinical Research Associate Zp Group LlcOncology Clinical Research AssociateChicago, IL$100,000–$120,000 / yearKeywords: Clinical Research Associate, CRA, Clinical Trials, Site Monitoring, EDC Systems, Oncology Research, GCP, ICH Guidelines, Study Start-Up, Remote Monitoring, On-site Monitoring, Clinical Operations, Protocol Compliance, Data Review, Regulatory Oversight, CRO, Clinical Development, Trial Management, Multi-site Studies, Investigator Relations, Monitoring Visits, Risk-Based Monitoring, Clinical Documentation, Pharma Research, Biotech Studies, Data Integrity, Study Activation, Research Compliance, Trial Oversight, Drug Development, Clinical Systems. The Oncology Clinical Research Associate will play a vital role in managing investigative sites and ensuring the successful delivery of clinical studies across a national footprint, with an emphasis on high-quality data and regulatory compliance.
Senior Clinical Research Associate - Psychedelics - Central U.S. (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Psychedelics - Central U.S. (Remote)ILRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Senior Clinical Research Associate - Psychiatry - Central U.S. (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Psychiatry - Central U.S. (Remote)ILRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Senior Clinical Research Associate - Obesity - Central U.S. (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Obesity - Central U.S. (Remote)ILRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Senior Clinical Research Associate IRESenior Clinical Research AssociateChicago, Illinois$110,520–$138,150 / yearPerform remote and on-sitemonitoring/co-monitoringvisits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials. Senior Clinical Research Associate - Oncology Phase I - Chicago ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available Thermo Fisher ScientificExperienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas AvailableChicago, IllinoisMonitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
Clinical Research Associate - Start up - Cross TA IREClinical Research Associate - Start up - Cross TAChicago, Illinois$91,336–$114,170 / yearClinical Research Associate (Start up) - Cross Therapeutic Area- Illinois ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Collaborate with country operations teams to identify, select, and activate clinical trial sites in accordance with project timelines and requirements.
Clinical Research Associate Zp Group LlcClinical Research AssociateChicago, ILRemote$120,000–$135,000 / yearThe Clinical Research Associate will function as the primary bridge between sponsors and sites, ensuring clinical trials follow protocols, protect patients, and meet all regulatory expectations to succesffuly create lifesaving drugs and treatments. Piper Companies is actively seeking Clinical Research Associates to join a top‑tier CRO with a proven track record of excellence, trusted by global pharma and biotech partners.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateChicago, IL$110,520–$138,150 / yearPerform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites.
Clinical Research Manager, Research Incubation Unit University of ChicagoClinical Research Manager, Research Incubation UnitChicago, IL$90,000–$130,000 / yearThe Clinical Research Incubation Unit was established to enable growth of clinical research portfolios across the Biological Sciences Division as well as provide timely research staffing services to departments or units in need of short-term clinical research management services. The mission of the Office of Clinical Research 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.
Clinical Research Associate - Start up - Cross TA ICON PlcClinical Research Associate - Start up - Cross TAChicago, IL$91,336–$114,170 / yearCollaborate with country operations teams to identify, select, and activate clinical trial sites in accordance with project timelines and requirements. Coordinate with the country operations team to collect essential documents (such as regulatory approvals and contracts) to enable timely site activation.
Clinical Research Associate, Cardiology Northwestern UniversityClinical Research Associate, CardiologyChicago, ILThe candidate will need to ensure that all study activities are completed by strictly following Good Clinical Practices (GCP) and all current local, state, and federal laws, regulations, guidance, policy & procedure developed by the Northwestern University Institutional Review Board (IRB), Food and Drug Administration (FDA) Code of Federal Regulations (CFR), and the International Conference on Harmonization (ICH). This may involve recruiting subjects for studies, preparation and submission of IRB regulatory materials, preparation and submission of OSR documents, administering tests &/or questionnaires; collecting, compiling, tabulating &/or processing responses; gathering information; &/or assisting in the preparation of material for inclusion in reports.
Senior Clinical Research Associate (level dependent on experience) CTISenior Clinical Research Associate (level dependent on experience)Chicago, IllinoisFor that reason, we treat our team members with the respect they deserve, and our numbers show it: We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward. To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance.
Clinical Research Associate II - Oncology, Ophthalmology & Neurology - Central US Thermo Fisher Scientific IncClinical Research Associate II - Oncology, Ophthalmology & Neurology - Central USChicago, IL$66,800–$125,000 / yearWhat You'll Do: Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
Clinical Research Quality Assurance and Improvement Specialist Ann & Robert H. Lurie Children's Hospital of ChicagoClinical Research Quality Assurance and Improvement SpecialistChicago, IllinoisThe Clinical Research Quality Assurance and Improvement (QA/QI) Specialist utilizes knowledge to 1) analyze and interpret applicable regulations, 2) develop/revise institutional policies and procedures, 3) audit the conduct of human subjects research (biomedical, social & behavioral) and research oversight programs, 4) assess compliance with all applicable regulations, guidances, and policies and procedures, 5) identify areas of risk, and 6) oversee the development and implementation of corrective and preventive action plans. forms and checklists, educational training, regulatory advice/consultation, etc.) for investigators, research staff and other members of the HRPP to promote the responsible conduct of research and assists with site or study-specific self-assessments.
Clinical Research Associate Northwestern UniversityClinical Research AssociateChicago, ILThis role will involve operational and scientific contributions to the Implementation Intelligence Lab, partnering with the Northwestern Medicine Information Services team to develop and embed AI tools into clinical care, validating third-party tools for regulatory approval, and partnering with Feinberg School of Medicine stakeholders and NUCATS (Northwestern University Clinical and Translational Sciences Institute) to build infrastructure for scalable AI research and deployment. The Institute for Artificial Intelligence in Medicine (I.AIM) at Northwestern University Feinberg School of Medicine seeks a full-time Clinical Research Associate to manage and contribute to a research portfolio in the areas of artificial intelligence and cardiovascular disease, with a particular focus on development and implementation of digital health tools to address health care delivery problems and support research infrastructure.
Clinical Research Associate - Cross TA IREClinical Research Associate - Cross TAChicago, Illinois$75,480–$94,350 / yearWilling and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in Illinois near major HUB airports to support efficient regional travel. Clinical Research Associate- Cross Therapeutic Area- Chicago ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Associate II IREClinical Research Associate IIChicago, Illinois$91,336–$114,170 / yearWilling and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in Chicago near major HUB airports to support efficient regional travel. Clinical Research Associate- Oncology- Chicago ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Coordinator Assistant InsightClinical Research Coordinator AssistantChicago, IllinoisPerforms technical requirements of the study protocol, i.e., lab work (phlebotomy and processing), blood pressure, electrocardiograms, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or specified by a protocol. The CRC assistant will support the CRC, administrative staff and principal investigators, assist the communications between sponsor and institute, oversee details of clinical studies and ensure compliance with study review board and clinical research regulations.