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Remote Clinical Research Associate Jobs in New Jersey

Clinical Research Associate Jobs
By Talencio At Greater Minneapolis-St. Paul Area, United States
Clinical Trial Collaboration: Work alongside our clinical team, focusing on site qualification, initiation, management, and data integrity.
Data Management: Oversee data activities, generate, and resolve queries, and report on study metrics including enrollment and adverse events documentation.
Regulatory Oversight: Manage investigational product accountability, monitor IRB requirements, and ensure prompt processing of regulatory documents.
Bachelor’s degree in a medical/scientific field, with 4+ years of clinical research experience (Master’s degree can substitute for 1 year).
Strong organizational, multitasking, and relationship-building abilities.
Effective communication skills and keen attention to detail.
Clinical Research Associate Jobs
By Agilent Technologies At Trenton, NJ, United States
Assist with site audits and site quality management activities, as needed.
Ensure monitoring activities (remote and on-site) are completed in accordance with Agilent procedures and study monitoring plan.
Assures adherence to GCP, study protocol, and all applicable requirements through routine monitoring visits.
3+ years direct clinical research experience at a sponsor or CRO as a CRA/study monitor, or equivalent experience.
Diagnostic/IVD experience highly preferred, oncology or other medical device experience is also accepted.
Previous experience with NGS, IHC, or pathology highly preferred.
Research Analyst, Gt.school (Remote) - $60,000/Year Usd
By Crossover At Elizabeth, NJ, United States
Understand the importance of revolutionizing the education space with cutting-edge technology.
Excellent written and verbal English communication skills
2+ years of work experience working in a technical field (science, technology, financial services, data science)
Are strategic problem solvers who can quickly devise and implement solutions to address ad-hoc issues facing our students
Consider themselves to be consistent, high performers who rarely have ‘off-days’.
Converting important decisions made by leadership into work units that a junior Operations team can perform.
Research Analyst, Gt.school (Remote) - $60,000/Year Usd
By Crossover At New Jersey, United States
Understand the importance of revolutionizing the education space with cutting-edge technology.
Excellent written and verbal English communication skills
2+ years of work experience working in a technical field (science, technology, financial services, data science)
Are strategic problem solvers who can quickly devise and implement solutions to address ad-hoc issues facing our students
Consider themselves to be consistent, high performers who rarely have ‘off-days’.
Converting important decisions made by leadership into work units that a junior Operations team can perform.
Sr. Clinical Research Associate (Seattle Only)
By Thrive At Greater Seattle Area, 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
Phases I-IV ONCOLOGY Trial experience
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
Clinical Research Associate Jobs
By Hays At Paramus, NJ, United States
• Ability to effectively interact with and support all levels of management
• Conduct site qualification, monitoring, close-out, and monitoring oversight visits
• Good Clinical Practice (GCP) and ICH certification preferred
• Knowledge of the pharmaceutical industry and the drug development process
• At least 2 years on-site monitoring experience in Clinical R&D
• Knowledge of clinical research policies and procedures
Clinical Research Associate Jobs
By Jupiter Research Services LLC At Edison, NJ, United States
Edison, New Jersey 08817 or Remote or Hybrid
highly qualified, experienced, and passionate professionals, dedicated to providing unparalleled customer service
·Experience hosting/performing internal and external audits is preferred
·Oncology, Ophthalmology and Metabolic Diseases experience
·Minimum 3 years of experience as an independent CRA
8 Hours/day or more as needed
Clinical Research Associate Jobs
By Bionical Emas At Paulsboro, NJ, United States
Previous experience that provides the knowledge, skills, and abilities to perform the job
The CRA will complete all role specific required training and documents needed in the applicable learning management system
Previous independent monitoring experience is essential
They will comply all applicable Bionical Emas SOPs and policies
Completes and submits timesheet and expenses in a timely manner, as per company guidelines
When necessary, they will be a mentor to other CRAs
Clinical Research Medical Director (Remote)
By Novartis At , East Hanover, 07936, Nj $257,600 - $386,400 a year

22. The number of dedicated and inspired professionals in the US Clinical Execution team who are empowered to ask new questions and make bold decisions to bring lifesaving medicines and ...

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