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Remote Clinical Research Associate Jobs in Illinois

Clinical Research Associate Jobs
By Invenio Clinical At Illinois, United States
Oversee site management responsibilities for assigned sites.
Assist in the management of routine trial activities, adhering to industry and corporate standards.
Support the Study Team/Management in all phases of the clinical trial.
Manage trial-specific Trial Master File (TMF) and internal filing system, including regulatory and legal document tracking and archiving.
2+ years of experience in a sponsor or CRO setting (strongly preferred).
Knowledge of clinical research in Cardiology/Medical Devices
Clinical Research Associate I - Remote (Usa Only)
By Abbott At Illinois, United States
Must be detail-oriented and efficient in time management.
Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol.
Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff.
Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
Basic knowledge in regulations for applicable geographies and types of studies (IDE, non-significant risk, feasibility, exempt, etc.).
Minimum 1-year clinical research experience required.
Clinical Research Associate Jobs
By SRG At Chicago, IL, United States
Excellent organization skills with attention to details and time management, bringing forward ideas and paths for building on organizational tools
Excellent written and verbal communication and interpersonal skills
Consistently creates pathways for process improvement, streamline workflows and build efficiently for individual and project outcomes with little guidance from manager
Works within timelines with limited oversight from manager, informing managers of any potential issues with timelines, bringing solutions/mitigations as necessary
Manage drafting and finalization of protocol and associated documents, including identifying need for amendments
Collect, manage, file and archive study documentation and correspondence. Assist in the accuracy and completeness of the Trial Master Files (TMF)
Senior Clinical Research Associate (Dermatology)
By Ergomed At , Cary, Nc
College/University degree in Life Sciences or an equivalent combination of education, training & experience
Communication, collaboration, and problem-solving skills
To act as the main point of communication with Investigator and his team
When requested to support preparation of regulatory and / or EC submission
Participate in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance
Full working proficiency in English
Senior Clinical Research Associate
By Ergomed At , Cary, Nc
College/University degree in Life Sciences or an equivalent combination of education, training & experience
Communication, collaboration, and problem-solving skills
To act as the main point of communication with Investigator and his team
When requested to support preparation of regulatory and / or EC submission
Participate in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance
Full working proficiency in English
Clinical Research Associate Jobs
By Castle Biosciences, Inc. At Elk Grove Village, IL, United States
M-F; working remotely from home, Midwest USA-based location, near a major airport; travel routinely 50-60% and up to 80% at times.
Bachelor's degree in a science or healthcare-related field or a registered nursing certification or equivalent certification/licensure from an appropriately accredited institution.
3 years of CRC experience or previous 1-year experience as a CRA.
Direct patient care or clinical research experience required.
Familiarity with clinical research and study development processes.
Valid Driver's License where applicable.
Clinical Research Associate Ii
By Visby Medical At , San Jose, 95134, Ca $95,000 - $125,000 a year
Collaborate with Data Manager and/or Clinical Affairs management to define data management plan and design CRFs.
Computer software skills (e.g., MS Word, Excel, PowerPoint and Google products experience).
Knowledge of FDA requirements for clinical validation and CLIA waiver.
Minimum 3 years of related experience, preferably including clinical research and clinical operations experience.
Experience working in IVD clinical studies highly preferred.
Strong attention to detail, self-motivation, and good organizational skills.

Are you looking for a unique opportunity to make a difference in the healthcare industry? We are seeking a Remote Clinical Research Associate to join our team and help us develop innovative treatments for patients. You will be responsible for monitoring clinical trials, ensuring compliance with protocols, and providing support to investigators and sponsors. If you have a passion for clinical research and want to make a real impact, this is the job for you!

Overview A Remote Clinical Research Associate (CRA) is a professional who is responsible for the management and coordination of clinical trials. The CRA is responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP). The CRA is also responsible for monitoring the progress of the clinical trial, ensuring that the data collected is accurate and complete, and reporting any adverse events or other issues to the sponsor. Detailed Job Description

The Remote Clinical Research Associate is responsible for the management and coordination of clinical trials. This includes:

• Developing and maintaining relationships with clinical sites and investigators
• Ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP)
• Monitoring the progress of the clinical trial
• Ensuring that the data collected is accurate and complete
• Reporting any adverse events or other issues to the sponsor
• Assisting in the preparation of regulatory documents
• Assisting in the preparation of clinical study reports
• Assisting in the preparation of data for submission to regulatory authorities
• Assisting in the preparation of presentations for investigators and other stakeholders
• Assisting in the preparation of training materials for investigators and other stakeholders
• Assisting in the preparation of budgets and contracts
• Assisting in the preparation of study materials
• Assisting in the preparation of study protocols
• Assisting in the preparation of informed consent forms
• Assisting in the preparation of study reports
• Assisting in the preparation of study databases
• Assisting in the preparation of study manuals
• Assisting in the preparation of study monitoring plans
• Assisting in the preparation of study closure documents
Job Skills Required
• Excellent communication skills
• Strong organizational skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize workload
• Knowledge of clinical trial regulations and Good Clinical Practices (GCP)
• Knowledge of clinical trial processes and procedures
• Knowledge of clinical trial data management
• Knowledge of clinical trial software
• Knowledge of medical terminology
• Knowledge of medical devices
• Knowledge of clinical research terminology
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification as a Clinical Research Associate (CRA)
Job Knowledge
• Knowledge of clinical trial regulations and