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Apex 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.
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

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? Apex Clinical Research is looking for a Clinical Research Associate to join our team and help us make a difference in the lives of patients. As a Clinical Research Associate, you will be responsible for managing clinical trials, ensuring compliance with regulatory requirements, and providing support to clinical teams. If you have a passion for clinical research and want to make a difference, this is the job for you!

Overview Apex Clinical Research Associates are responsible for conducting clinical research studies in a variety of settings. They are responsible for collecting and analyzing data, preparing reports, and presenting findings to stakeholders. They must be knowledgeable in clinical research protocols and regulations, and must be able to work independently and collaboratively with other members of the research team. Detailed Job Description Apex Clinical Research Associates are responsible for conducting clinical research studies in a variety of settings. They are responsible for designing and implementing research protocols, collecting and analyzing data, preparing reports, and presenting findings to stakeholders. They must be knowledgeable in clinical research protocols and regulations, and must be able to work independently and collaboratively with other members of the research team. They must also be able to communicate effectively with research participants and other stakeholders. Job Skills Required
• Knowledge of clinical research protocols and regulations
• Ability to design and implement research protocols
• Ability to collect and analyze data
• Ability to prepare reports and present findings
• Ability to work independently and collaboratively
• Excellent communication and interpersonal skills
Job Qualifications
• Bachelor’s degree in a related field
• Previous experience in clinical research
• Knowledge of clinical research protocols and regulations
• Ability to design and implement research protocols
• Ability to collect and analyze data
• Ability to prepare reports and present findings
• Ability to work independently and collaboratively
• Excellent communication and interpersonal skills
Job Knowledge Apex Clinical Research Associates must have a comprehensive understanding of clinical research protocols and regulations. They must be knowledgeable in the design and implementation of research protocols, data collection and analysis, and report preparation and presentation. Job Experience Apex Clinical Research Associates must have previous experience in clinical research. They must be able to work independently and collaboratively with other members of the research team. Job Responsibilities
• Design and implement research protocols
• Collect and analyze data
• Prepare reports and present findings
• Communicate effectively with research participants and other stakeholders
• Ensure compliance with clinical research protocols and regulations
• Work independently and collaboratively with other members of the research team