UNKNOWN

FEED

Conduct all types of monitoring visits: Pre-Site Selection Visits (PSSVs), Study Initiation Visits (SIVs),Interim Monitoring Visits (IMVs) and Closeout Visits (COVs). Working closely with investigative sites, sponsors, and cross-functional study teams, you'll drive study quality, support patient safety, and help bring innovative therapies closer to those who need them most.

YEAR

Worldwide Clinical Trials Holdings Inc

Senior Clinical Research Associate - CNS/Psychiatry - Central U.S.

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Key responsibilities include: Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

Clinical Research Associate

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Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks. Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File (TMF) documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics.

Parexel

Sr. Clinical Research Associate - US - Midwest/Central Region - FSP

The Project Manager-Clinical Trials has primary responsibility over the management of multiple clinical research trials, to include selection and analysis of potential patients for study participation, obtaining informed consent, documentation of all study required case report forms, identifying potential adverse events and reporting them to FDA/IRB/Study Sponsor as applicable. Other benefits include: Wellness program with incentives, employer-paid life insurance and short-term and long-term disability coverage, flexible spending accounts, employee assistance program, ID theft coverage, colleague rewards and recognition program, discount program, and more!

HOUR

Hospital Sisters Health System - Corporate

Project Manager-Research,

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Hospital Sisters Health System

Methodological expertise: Proven track record of developing or implementing advanced analytical methods (e.g., target trial emulation, propensity score applications in complex cohorts, causal inference, or machine learning-augmented epidemiology) and creative problem solving. Client Strategy & Partnership: Partner with Key Account Directors and Business Development to identify opportunities where novel methodology can solve "unsolvable" client problems (e.g., rare disease characterization or complex biomarker validation).

Tempus AI

Associate Director, Outcomes Research

You will complete a short screening form so our system can match you with relevant consumer research opportunities within our national insights program. All tasks are conducted online and can be completed outside traditional business hours.

Occupons Quebec

Remote Market Research Participant Up to $90/Session No Experience Required

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Specific priorities include relationship development with Key Opinion Leaders (KOLs), leading new clinical site launches, identifying new clinical research partners, and developing strategic plans for research partnerships within territory. Clinical Site Management & Enrollment: act as the primary point of contact for clinical trial sites, proactively driving patient enrollment and ensuring study milestones are met.

At Abbott, we are enthusiastic, energetic and committed to doing great work every day. Our employees are passionate about helping to translate science into lasting contributions to health care and the health of people worldwide. At the heart of our organization is our "Promise for Life"&mdash;a statement that embodies our company's commitment to employees, shareholders, local communities and the people who depend on our company and products to live healthier lives.
 
Vital to our promise is the speed in which we act, respond and deliver. As Abbott employees, we are ready to meet change and challenges head-on. As a result, we are a company that adapts quickly, and through our passion for innovation we are able to continually create a pipeline of products that help improve the length and quality of life around the world.
 
We are proud of our rich, more than 120-year history. We continue to be driven to advance leading-edge science and technologies, support diversity, focus on exceptional performance and earn the trust of those we serve.

Abbott

Regional Clinical Affairs Manager - Electrophysiology

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10 years’ experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. Analyze and communicate technical and clinical product specification requirements from luminaries, market research teams, and via Medical Advisory Boards (MABs) to global business team.

Canon USA & Affiliates

Leader Medical Affairs

Our client specializes in bringing clinical trials directly to patients through decentralized and hybrid clinical trial models, helping reduce geographic, logistical, and socioeconomic barriers to research participation. RPM ReSearch has been engaged by an innovative global clinical research organization to identify experienced Registered Nurses who are passionate about patient care and interested in supporting the future of medicine.

RPM ReSearch

Registered Nurse (Part-Time) - Silvis, IL

As the TMVR Imaging Analysis Manager, you will lead the team that conducts imaging analysis in support of the patient selection and screening processes for clinical studies associated with Abbott Structural Heart Devices and Products, particularly Transcatheter Mitral Valve Replacement (TMVR). The incumbent will work closely within the internal clinical study team, including the clinical science, project management, field clinical affairs, medical affairs, biostatistics, study management, and data management, as well as with external investigators.

Research Jobs in Archer, IL

Senior Clinical Research Associate - CNS/Psychiatry - Central U.S. Worldwide Clinical Trials Holdings Inc

Clinical Research Associate IRE

Sr. Clinical Research Associate - US - Midwest/Central Region - FSP Parexel

Project Manager-Research, Hospital Sisters Health System - Corporate

Project Manager-Research, Hospital Sisters Health System

Associate Director, Outcomes Research Tempus AI

Remote Market Research Participant Up to $90/Session No Experience Required Occupons Quebec

Regional Clinical Affairs Manager - Electrophysiology Abbott

Leader Medical Affairs Canon USA & Affiliates

Registered Nurse (Part-Time) - Silvis, IL RPM ReSearch

Manager, TMVR Imaging Analysis Abbott

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