Clinical research jobs in Linden, 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...

Escalates as needed different challenges and issues to TA Head/CRD Clinical Research Director/CCQM Country Clinical Quality Manager and or CTT Clinical Trial Team (as appropriate). Behavioral Competency Expectations: Strong leadership skills that enable and drive alignment with the goals, purpose...

The 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. This role will perform a variety of clinical and administrati...

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...

Join an award-winning team of dedicated professionals committed to our core values of quality, compassion and community! Saint Michael's Medical Center, a member of Prime Healthcare, offers incredible opportunities to expand your horizons and be part Clinical Research, Research Associate, Researc...

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...

Description:Job Summary: Looking to hire an individual with a nursing or clinical research background to act as the Clinical Research Coordinator for a research site in Newark, NJ on an Ophthalmology clinical trial. Duties and Responsibilities:- Chart review of patient's medical recordso EMR- mus...

Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Under the direction of supervisor or designee, this position will ser...

To discover more on our scientific and technical functions at L'Oréal Research & Innovation, please check out our websiteWe are seeking a Scientist with an innovative mindset to join our Photoprotection Clinical and Physics (Instrumental) Sciences Evaluation Intelligence Team in our Clark, New Je...

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. Under the direct supervision of the Nurse Manager of Clinical Research Ce...

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. Contract Research Organization, health sciences/biotechnolo...

Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated site...

Director (Principal Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our company's Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). Evaluating pre-clinical...

Vitalief was formed to address any concerns the clinical trial industry is facing today. We are expanding our footprint rapidly as a value-added, innovative Research and Clinical Trial Consulting ...

This position is responsible for the supply planning and inventory management of clinical supplies required to support global clinical research and development studies during phases 1-4. The ...

With support of Sr CRA (Clinical Research Associate) and/or CRA Manager, acts as primary site contact and site manager-throughout all phases of a clinical research study, taking responsibility of ...

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 ...

A Clinical Outcome Assessment (COA) Instrument is a standardized formal perception-based clinical ... PhD in Health Services Research, Statistics, Psychometrics, Outcomes Research, or closely related ...

... Research, Statistics, Psychometrics, Outcomes Research, or closely related field with 3+ years of ... into clinical trial and observational studies • Ability to understand and respond to multiple ...

The Clinical Nurse Educator is responsible for designing, teaching, and evaluating and executing ... and research to address both the clinical and social determinants of health. RWJBarnabas Health ...

We are partnered with NJMS to broaden the reach of our patient care and expand our ability to perform clinical research using the full scope of resources available in the schools research support ...

Maintaining strong relationships with internal and external partners (CROs, global Advanced Research, Data Management Team, and Statistical Team), to ensure clinical study integrity. * Serve as key ...

Responsibilities include patient care, supervision of residents and medical students, and participation in clinical research. There is an 8-bed accredited Sleep Center, an Asthma Center, a PFT lab ...

As a key member of our clinical research company, you will play a crucial role in overseeing and conducting clinical trials. In this role you will ensure protocols adhere to regulatory requirements ...