Remote clinical research associate jobs in Englewood, New Jersey (NJ) State

The Assistsnt Project Manager will be responsible for:Project Planning and Scheduling:Assist in defining project scope, goals, and deliverables that support business goals in collaboration with senior management and stakeh...

Certified Clinical Research Professional or Certified Clinical Research Coordinator or Certified Clinical Research Administrator. Works daily in collaboration with other research team members including but not limited to Principal Investigators, Research Nurse Coordinators, Clinical Research Coor...

Works daily in collaboration with other research team members including but not limited to Principal Investigators, Research Nurse Coordinators, Clinical Research Coordinator, Clinical Data Coordinator, Sponsors, Contract Research Organizations, and employees of Hackensack University Medical Cent...

Performs background research for manuscripts, publications, and research projects. HMH)as an academic basic and translational research enterprise to rapidly translate science innovation to the clinic and to improve outcomes for patients with cancer, infectious diseases, autoimmune disease and oth...

Providing technical expertise in data storage structures, data mining, and data cleansing. As a Data Analyst, you will directly work with key client stakeholders to define the business problems, analysis requirements, and determine solution requirements. Manage and design the reporting environmen...

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...

Identify valuable data sources / data sets that can be leveraged to improve results. Data Scientist with proven track record . Work with stakeholders, identifying opportunities for leveraging data to solve for business challenges. Analyze data to interpret against business opportunity and discove...

Input, update, and maintain accurate data into our computer systems or our database. As a Data Analysis, you are responsible for making sure files are up to date and correctly input information into our system. Data Entry Analysis Core Qualifications:. Data Entry Clerk Core Responsibilities:. ......

Consultant and Data Analyst, Philanthropy Insights and Analytics (PIA). The Consultant and Data Analyst reports to the Vice President for Philanthropy Insights and Analytics and works closely with the Philanthropy Insights & Analytics team and consultants across the firm. Demonstrated knowledge o...

Description:* Manages multiple investigator-initiated clinical trials. Builds research infrastructure to support multi-center clinical trials. Experience in clinical protocol and trial document development. Oversees and drives projects from concept to final deliverables in form of publications, c...

Award-winning and growing CRO seeks a Quality Assurance Manager to oversee the Clinical Trials Laboratory with Phase 1 Clinical trail CRO QA expertise being a must. Clinical Trials Quality Assurance Manager – (Full-time) – Onsite – NJ. This requires 5+ years’ experience in clinical trials and res...

Acts as a project resource to the clinical site, sponsor, and personnel regarding the product under test and the clinical trial conduct. May function as the Lead Monitor on assigned clinical trials to ensure adherence to Federal regulations, clinical protocol, company policies, and any other appl...

Director of Operations / Vice President of Operations / VP of Ops / Senior Director of Quality / Senior Director of QA / Plant Manager / Site Director / Director of Clinical Services / Director of Clinical Trial Supply / Head of Clinical Packaging / General Manager / Director of Clinical Trial Su...

We are searching for a (Senior) Translational Data Scientist. You will work on the following data types; clinical response, tumor transcriptomic/genetic data as well as imaging and circulating biomarkers to support various drug candidates. Utilising various cutting-edge data science tools; AI, ML...

The role involves maintaining the department Project Staffing list and ensuring its accuracy. Demonstrates strong project management skills. ...

The Axel Group, LLC is hiring for an Assistant Project Manager position in Belleville, NJ. Project Coordination: Assist in the preparation of project plans, schedules, and budgets. Communication: Serve as a liaison between the Project Manager, site personnel, and stakeholders. Documentation and R...

Accurately input and update data into databases and spreadsheets. Follow data entry procedures and protocols to ensure data integrity. Verify data for accuracy and completeness, making corrections as needed. Assist in generating reports and performing data analysis when required. ...

Role: Solar Development Project Manager. They are building out their team in the US and one of their key hires is a Solar Development Project Manager. Monitor project performance metrics and take corrective actions to achieve project goals. Proven experience managing utility scale solar energy pr...

Acts as a project resource to the clinical site, sponsor, and personnel regarding the product under test and the clinical trial conduct. May function as the Lead Monitor on assigned clinical trials to ensure adherence to Federal regulations, clinical protocol, company policies, and any other appl...

Apply remote type Remote locations USA - New Jersey - Rahway USA - REMOTE - REMOTE USA - Pennsylvania - North Wales (Upper Gwynedd) time type Full time posted on Posted 3 Days Ago job requisition id R285039. Associate Director, Clinical Quality Operations, (Re...

Senior Clinical Research Associate. Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...

Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines. CRAs are to complete all aspects of the clinical monitoring process in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs. Perform and coordinate assigned aspects of...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Location: While this role is remote/hybrid, c...