Clinical research coordinator jobs in North Bergen, New Jersey (NJ) State

Position OverviewThe Travel Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator. What You'll Be Working OnThis role will perf...

Clinical Research Nurse Opportunity with a highly ranked cancer institute in NJ! Apply now for more information! Must Haves:+ RN+ 2+ Years Related ExperienceJob Summary and Responsibilities:The Clinical Research Coordinator, RN is responsible for coordinating and overseeing clinical operations of...

Required qualifications, capabilities, and skill Formal training or certification on software engineering concepts and 5+ years applied experience Expert knowledge in all business processes across an entire line of business, as well expertise in other lines of business and technology disciplines ...

The Project Coordinator will be responsible for ensuring that customer queries, projects and issues are dealt with efficiently and in a professional manner. Northern Architectural Systems is looking for a Project Coordinator, who possesses an understanding of engineering concepts, to assist in de...

Conduct thorough research, create experimental designs, gather supporting data, and perform statistical analysis for new products and solutions. ...

Neighborhood Program Coordinator. Designed to expand existing programs and invent new scalable and replicable models, the Center serves as a think-tank for innovative ideas to address social and economic inequities and actively catalyze societal change – all of which creates measurable equity and...

Provide administrative support to the site management and the clinical staff. ...

Research new projects, create experimental designs, collect data, and analyze statistics for new products and solutions. ...

Main Skills: IT Project Manager, managing client server software development projects (BI, Data Analysis), vendor management, bank operations or market research in banking. Work with the external vendor to make sure project is in scope and no billing is outside scope of services. Good understandi...

Conduct research on newly assigned projects, build experimental designs, collect supporting data, and complete statistical analysis for new products and solutions. ...

Beyond this, you’ll have many opportunities to get the hands-on experience and credentials medical assistants require in the civilian world. ABOUTMedical emergencies happen and we need people who can take charge when they do. Whether you’re in a hospital or clinical setting, on a ship or submarin...

Candidate should have deep understanding of Project management. Defining the Project Management Methodology. Candidate should have deep understanding of project metrics and reporting. ...

We are currently seeking a highly organized and detail-oriented Coordinator to join our team. As a Coordinator, you will play a crucial role in supporting various departments and ensuring the smooth operation of daily activities. Coordinate and facilitate communication between different departmen...

Ensures compliance with protocol and all regulatory policies, procedures, and/or guidelines during clinical studies by training/guidance of investigators/research coordinators, conducting periodic on-site evaluations, and follow-up of corrective actions. Trains contract research organizations (CR...

Job Title: Business Analyst / Project Manager. Business Analyst with strong Project Management and data modeling experience Agile; SQL Experienced with Agile mythology, process flow and solid understanding of creating stories, epic and deliverable Knowledge of SQL queries and MS office applicatio...

Association of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP) preferred. IMMEDIATE NEED FOR CLINICAL RESEARCH NURSENeed Oncology and Phase I experienceThe primary purpo...

Thorough understanding of ICH Good Clinical Practices, clinical trials management and regulatory compliance as it relates to clinical operations. Candidate must have clinical study site experience (phase I-IV preferred) in order to have a thorough understanding of the processes associated with cl...

Thorough understanding of ICH Good Clinical Practices, clinical trials management and regulatory compliance as it relates to clinical operations. Candidate must have clinical study site experience (phase I-IV preferred) in order to have a thorough understanding of the processes associated with cl...

Occasionally attending out-of-town Investigator Meetings Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent Facilitate...

SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studie...

Certified Clinical Research Professional or Certified Clinical Research Associate or Certified Clinical Research Coordinator. In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates pot...

The system is known as a high-quality, low-cost provider of extraordinary clinical care given by compassionate, highly trained physicians and staff. Working under the direction of the Principal Investigator (PI), responsible for the overall coordination and administration of daily activities of I...

Required Skills: Minimum of 1 to 2 years of experience in Clinical Research as a Clinical Research Coordinator, with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance and data management. Job Responsibilities: Under the direct supervision of th...

Clinical Research Coordinator I The  CRC I  will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Liaising with Laboratory team...