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Remote Clinical Research Associate Jobs

Clinical Research Associate, Sponsor Dedicated
By IQVIA At , Remote
Alternatively, you should have an equivalent combination of education, training and experience
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
2 years of clinical research coordinator experience strongly preferred
While projects vary, your typical responsibilities might include:
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
Higher Ed Consulting Associate - Huron Research Suite (Remote) ($95000.00 - $125000.00 / Year)
By Talentify.io At United States
Opportunity to collaborate with education organizations and drive growth and performance in the market.
Gain valuable consulting experience and opportunities for career growth.
Develop requirements, test cases, and testing plans while bridging functional and technical roles.
Minimum of 3 years of experience as a Business Systems Analyst or similar role.
Experience in software implementation is preferred.
Knowledge of research administration, research strategy/transformation, research operations, and/or regulatory compliance is a plus.
Excellent Job Opportunity For Role: Clinical Research Associate At Alameda, Ca
By Intellectt Inc At Alameda, CA, United States
Must have 5+ years of relevant experience in site monitoring, clinical project management, clinical trial practices and regulations.
Proactively and effectively communicate the status of clinical studies to management.
Clinical Operations Manager as needed
TMF upload experience is preferred.
Experience coordinating site initialization and site close
Experience editing/revising CRF "case report forms"
Clinical Research Coordinator Crc - Remote | Wfh
By Get It Recruit - Healthcare At Pompano Beach, FL, United States

Are you passionate about making a difference in the field of healthcare? Do you thrive on engaging with patients and ensuring top-notch research protocols? We have an exciting opening for a Clinical ...

Lead Research Associate - Public Health - Remote
By Talentify.io At United States
Develop requirements for study and data management systems, including quality assurance and quality control measures.
Experience with bio-specimen collection and management is desired.
Strong organizational skills, including time management.
Obtain approvals and data source access, and oversee data acquisition and management.
Hiring Company offers a comprehensive benefits program focused on wellness and work/life balance.
Preferably experienced in multi-site epidemiologic studies.
Research Associate- Early Education- Remote
By Talentify.io At United States
Strong task management and organizational skills
Experience with data collection and management in applied settings
Apply your academic knowledge and work experience to lead and contribute to research and evaluation projects
Collaborate with colleagues to develop analytic plans and data management procedures
Familiarity with different meeting platforms, content management systems, and data systems
Opportunity to contribute to early education projects focused on child care, Head Start, pre-kindergarten, and military child care programs
Clinical Research Associate Jobs
By Lyra Therapeutics At Watertown, MA, United States

Lyra Therapeutics, Inc. is a clinical-stage biotechnology company developing novel, integrated drug and delivery solutions for the localized treatment of patients with chronic rhinosinusitis (CRS) ...

Research Associate, Clinical Biomarker Laboratory, Virus Neutralization Assays & Bio-Analytics
By Moderna At Norwood, MA, United States
Identify and resolve quality issues and report issues to upper management
Good computational skills, preferably experienced with Word, Excel, Power Point, GraphPad Prism
Conduct assay development, qualification/validation and sample analysis on a variety of platforms (ELISA, MSD, Ella, Automated ELISA Workstation etc.)
Assume assigned general laboratory responsibilities, e.g., safety coordinator, instrument/process/technology owner etc.
Bachelor or MSc in bioanalysis or related field with immunoassay experience preferably in a regulated environment
Good written, presentation, and interpersonal communication skills
Clinical Research Associate (Cra) - B
By Intellectt Inc At Alameda, CA, United States
5+ years of relevant experience in site monitoring and clinical project management.
Project management and organizational skills.
Communicate study progress to management.
Understanding of clinical trial process, data management, and analysis.
Manage clinical monitoring, site compliance, and adherence to protocols.
Experience in medical device, in-vitro diagnostics, or pharmaceutical studies.
Senior Manager, Clinical Research Monitoring (Remote)
By Edwards Lifesciences At , , Wi $123,000 - $174,000 a year
Excellent written and verbal communication skills including negotiating and relationship management skills with ability to drive achievement of objectives
Ability to interact professionally with all organizational levels and proactively escalate issues to appropriate levels of management in the organization
Provide direction and guidance to execute project deliverables in collaboration with project managers
Experience with electronic data capture preferred
Excellent problem-solving, organizational, analytical and critical thinking skills
Expert understanding of clinical studies procedures while addressing issues with impact beyond own team based on knowledge of related disciplines
Senior Clinical Research Associate (Usa)
By Premier Research At , Remote
4+ years of independent on-site monitoring experience with all types of site visits
We are Built by You. Your ideas influence the way we work, and your voice matters here
Identify and escalate potential risks and possible retraining opportunities for investigative sites.
Bachelor’s degree, or local equivalent, in a clinical, biological, scientific, or health-related field or its international equivalent
Completion of a CRA training program through a CRO
You must live in United States
Clinical Research Associate (Cra)
By LumaBridge At United States
Ability to independently prioritize tasks with excellent time management skills.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans.
Perform other duties as assigned by management.
Excellent verbal and written communication skills and conflict resolution abilities.
Oversee and conduct monitoring activities, including remote monitoring and risk-based monitoring.
Lead assigned sites through regular contact to ensure site compliance, adequate enrollment, and understanding of study requirements.
Clinical Research Associate Jobs
By WEP Clinical At Raleigh-Durham-Chapel Hill Area, United States
High organizational and logistics skills to ensure effective management of multiple sites and protocols within timeframes and on budget
Approximately 2-5 years of on-site and remote monitoring experience
Broad range of therapeutic experience
Superior written and verbal communication skills
Wren Nursing (Clinical Trial Home Nursing & Clinical Education)
Contribute to the development of protocols, study tools, materials, and documentation for clinical sites.
Clinical Research Associate Jobs
By ProTrials Research, Inc. At , $85,000 - $120,000 a year
Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training
Managing and training of site personnel on therapeutic area, protocol requirements, proper source documentation, and case report form completion
Excellent organizational skills, strong interpersonal and communications skills, and strong problem-solving skills
Extensive knowledge of FDA regulations and their practical implementation
2 years of prior experience as a Clinical Research Associate preferred
Full medical, dental, and vision benefit packages
Research Associate (Remote Or Hybrid)
By Moody's Corporation At New York, NY, United States
Excellent writing, presentation, project management and interpersonal skills are required.
The ideal candidate would have a BA degree in Finance, Statistics or Economics.
Ability to communicate technical subject matter clearly and concisely to individuals from various backgrounds is a plus.
Clinical Research Monitor (Remote, Midwest/Northeast Region) Tmtt
By Edwards Lifesciences At Greater Owensboro Area, United States
3 years of previous clinical research field monitoring experience OR, quality assurance/control and regulatory compliance experience, required
Experience working in a medical device or regulated industry, preferred
Experience with electronic data capture, preferred
Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are required
Demonstrated problem-solving and critical thinking skills
Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
Clinical Research Associate-208919 Jobs
By Medix™ At Florida, United States

The CRA is expected to work cooperatively with study team and operations management to proactively drive project success.

Research Assistant - Remote ($18.74 - $20.82 / Hour)
By Talentify.io At United States
Provide written and verbal feedback on outcomes projects to program management and staff
Adaptability to changing needs and willingness to acquire new skills and knowledge
Ability to gain a strong working knowledge of statistical methods and evaluation
Effective communication skills, both verbal and written
Experience or training in research and evaluation preferred
Monitor and process clinical outcome measures
Sr. Clinical Research Associate (12 Month Contract/Remote)
By Thrive At Raleigh, NC, United States
Assist with essential documents collection, review and archiving (TMF management)
Provide project management support for PTX project team, including vendor oversight
Conduct Site Initiation, Routine, and Close-out monitoring site visits, either on-site or remotely, prepare visit correspondence and records including trip reports
Oversee the conduct of assigned study sites, including ensuring compliance with SOPs, federal and local regulations, and ICH and GCP guidelines
Assist in the review and /or development of clinical trial documents such as study plans and training materials
Participate in and assist with facilitation of project team meetings
Sr. Clinical Research Associate (100 % Remote)
By Thrive At Cambridge, MA, United States
Assist with essential documents collection, review and archiving (TMF management)
Provide project management support for PTX project team, including vendor oversight
Conduct Site Initiation, Routine, and Close-out monitoring site visits, either on-site or remotely, prepare visit correspondence and records including trip reports
Oversee the conduct of assigned study sites, including ensuring compliance with SOPs, federal and local regulations, and ICH and GCP guidelines
Assist in the review and /or development of clinical trial documents such as study plans and training materials
Participate in and assist with facilitation of project team meetings

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