19 Clinical Operations Management jobs in Chicago.

Hiring now: Clinical Research Associa @ Johnson Jo, Clinical Ops Coordinator @ Northweste, Program Dir Translational @ Canning Th, Sr Practice Mgr @ Northweste, Clinical Research Coordin @ Care Acces, Program Mgr @ Tempus, Data Team Lead @ Iqvia, Patient Safety Leader @ Northweste, Clinical Research Coordin @ Nm, Sr Clinical Research Asso @ Parexel.Explore more at jobswithgpt.com.

🔥 Skills

project management (6) clinical trials (5) regulatory compliance (4) risk management (4) communication skills (4) Clinical Research (3) quality management (3) organizational skills (3) data management (3) communication (3)

📍 Locations

Chicago (16) Aurora (1) Bloomingdale (1) Elk Grove Village (1)

Johnson & Johnson

Skills & Focus: Clinical Research, GCP, Clinical Trial, Site Monitoring, Data Management, Regulatory Compliance, Study Documentation, Site Initiation, Patient Safety, Protocol Compliance
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: Experienced
Type: Fully Remote

Northwestern Medicine

Skills & Focus: clinical operations, supervision, patient care, resource allocation, staff coordination, service excellence, data accuracy, workflow management, staff training, performance appraisal

Canning Thoracic Institute

Skills & Focus: leadership, clinical trial strategy, research infrastructure, quality management, financial management, stakeholder engagement, project management, regulatory compliance, cross-functional collaboration, data coordination
About the Company: The Canning Thoracic Institute is part of Northwestern Medicine, focused on adhering to ethical standards and providing high-quality clinical trial strategy an…
Experience: Over 10 years of clinical research experience

Northwestern Memorial

Skills & Focus: clinical programs, management, staff supervision, resource allocation, data collection, cash management, financial analysis, budget communication, training and development, performance goals
About the Company: Northwestern Memorial reflects a commitment to the mission, vision, and values of Northwestern Medicine and adheres to rigorous compliance and ethical standard…

Northwestern Medicine

Skills & Focus: clinical trial strategy, research infrastructure, quality management, financial management, stakeholder relationships, regulatory compliance, cross-functional collaboration, educational programs, strategic planning, operational logistics
Experience: 10+ years of clinical research experience

Care Access

Skills & Focus: Good Clinical Practices, clinical trials, protocol compliance, patient coordination, recruitment, organizational skills, data management, medical terminology, regulatory compliance, communication
About the Company: Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that lim…
Experience: A minimum of 3 years prior Clinical Research Coordinator experience required
Type: Full-time
Benefits: Paid Time Off (PTO) and Company Paid Holidays, 100% Employer paid medical, dental, and vision insurance plan options, H…

Tempus

Skills & Focus: project management, biotechnology, clinical laboratory, medical device, project planning, regulations, leadership, communication, collaboration, risk management
About the Company: Tempus is on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings, specializing in precision medicine and advanci…
Experience: Minimum 3 years project management experience
Salary: $85,000 - $130,000 USD
Type: Full-time
Benefits: Full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits.

Iqvia

Skills & Focus: data management, clinical data management, project management, negotiations, quality management, financial tracking, process improvements, Good Clinical Practices, regulatory guidelines, compliance
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 5 years direct Data Management experience, including 3 or more years as a CDM project lead.
Salary: $82,300.00 - $173,900.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Northwesternmedicine

Skills & Focus: patient safety, high reliability, quality, adverse event follow-up, safety improvement, risk management, collaboration, metrics evaluation, clinical practice, interdisciplinary teams

Nm

Skills & Focus: Clinical Trial Coordination, Good Clinical Practice, Patient Care, Study Protocol, Adverse Events, Data Entry, Research Staff Training, Document Retention, Investigator Meetings, Study-Related Communication

Tempus

Skills & Focus: clinical data, data abstraction, project management, quality assurance, medical records, electronic data capture, oncology, data analysis, communication skills, healthcare technology
About the Company: Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical in…
Experience: 2+ years project management experience, 4+ years experience in a clinical or research setting.
Salary: $60,000 - $100,000 USD
Type: Full-time
Benefits: Full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits.

Care Access

Skills & Focus: clinical trials, recruitment, medical records, FDA regulations, ICH guidelines, Good Clinical Practices (GCP), data entry, phlebotomy, communication skills, organizational skills
About the Company: Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that lim…
Experience: A minimum of 1-year recent working experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant or Phlebotomist. Some Clinical Research experience preferred.
Type: Full-time
Benefits: PTO/vacation days, sick days, holidays; 100% paid medical, dental, and vision Insurance; 75% for dependents; HSA plan; …

Iqvia

Skills & Focus: monitoring, site management, Good Clinical Practice, study protocol, subject recruitment, documentation, data integrity, communication, regulatory submissions, clinical trial
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Requires at least 2 years of on-site monitoring experience.
Salary: $71,900.00 - $189,000.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs.

Parexel

Skills & Focus: Clinical Trials, CRA, Oncology, Functional Service Provider, Biostatistics, Statistical Programming, Finance, Clinical Research, Site Monitor, Remote

Tempus

Skills & Focus: Medical Director, Oncology, Clinical Trials, Study Design, Protocol Development, Multidisciplinary Teams, Clinical Research, GCP, Medical Expertise, Regulatory Interactions
About the Company: Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians.
Experience: 2+ years of clinical trials experience
Salary: $275,000 – $310,000 USD
Benefits: Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and o…
Skills & Focus: precision medicine, clinical care, real-world evidence, site engagement, operational initiatives, Subject Matter Expert, data integrity, tracking system, clinical research, FDA regulations
About the Company: Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical in…
Experience: 2+ years of clinical research experience in an oncology setting
Salary: $60,000 - $65,000 USD
Benefits: Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and o…

Novo Nordisk

Skills & Focus: clinical research, monitoring, clinical trials, data reliability, scientific integrity, regulatory compliance, patient safety, risk management, communication skills, stakeholder management
About the Company: At Novo Nordisk, you will help patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their…
Experience: A minimum of 4 years of clinical trial experience within a pharmaceutical, biotechnology, CRO, and/or healthcare setting is required; a minimum of 2 years of on-site monitoring experience is required.
Salary: $110K to $123K
Type: Full-time
Benefits: Medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accou…

The Alliance For Clinical Trials In Oncology Foundation

Skills & Focus: Translational Research, clinical trials, biospecimen, biomarker data sharing, project management, financial reporting, budget development, data management, communication skills, organizational skills
About the Company: The Alliance for Clinical Trials in Oncology Foundation is dedicated to enhancing cancer clinical research by conducting large-scale clinical trials that aim t…
Experience: 2-5 years of work experience in a related job discipline
Benefits: 8 weeks of paid time off, Medical, Dental & Vision plans with 100% employer-paid option, Tuition reimbursement stipends…

Johnson & Johnson

Skills & Focus: clinical trial agreements, clinical trials, negotiation, project management, analysis, contracting, budget management, stakeholder communication, risk management, legal compliance
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Type: Fully Remote