Clinical Trials Associate Jobs in New Jersey

i-Pharm Consulting - Pennington, NJ, United States

years of relevant experience as a clinical trial assistant or documentation specialist, or equivalent. Experience in the Pharmaceutical Industry or with a Contract Research Organization (CRO). Familiarity

from: linkedin.com - 13 days ago

Medasource - Hoboken, NJ, United States

of experience as a Clinical Research Associate Prior Cardiac Device trial experience Must have demonstrated strong written and verbal communication, interpersonal, presentation, analytical, organizational skills

from: linkedin.com - 7 days ago

US Tech Solutions, Inc. - Atlantic City, New Jersey

and coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. The Sr. CRC works collaboratively with the entire team, sponsors, and Clinical Quality Associates

from: resume-library.com - Yesterday

Blue Signal Search - Wood-Ridge, NJ, United States

. Provide support in administrative aspects of clinical trial conduct, ensuring compliance efforts are upheld. Skill Set: Bachelor's degree in a scientific or healthcare field. SOCRA-Certified Clinical

from: linkedin.com - 25 days ago

US Tech Solutions - Atlantic City, NJ, United States

is responsible for the oversight, facilitation and coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. · The Sr. CRC works collaboratively with the entire

from: linkedin.com - 29 days ago

Merck - Rahway, NJ 07065

biomarkers in late-stage clinical trials to support a potential companion diagnostic filing. Primary job responsibilities include: Determining and designing biomarker logistic and planning needs for late-stage

from: Pharmadiversityjobboard.com - 16 days ago

Net2Source Inc. - Rahway, NJ, United States

of patients. • How to collect patient data? • How do we make sure the correct questions are being asked to patients in the clinical trial? • Patient reported data. • Existing questionnaires to be included

from: linkedin.com - 24 days ago

Hackensack Meridian Health - Hackensack, New Jersey

and works under the general supervision of the principal investigator responsible for the clinical trials. Qualifications: Education, Knowledge, Skills and Abilities Required: BSN required. (Note

from: resume-library.com - 16 days ago

Daiichi Sankyo, Inc. - Bernards, NJ

with key stakeholders. Leverages comprehensive Data Management and medical coding expertise to promote best practices across the Clinical Trial lifecycle. Applies GCP principles to ensure all medical coding

from: Pharmadiversityjobboard.com (+1 source) - 3 days ago

Merck - Rahway, NJ 07065

surveillance activities such as aggregate clinical trial data analysis and post approval safety signaling reviews, using medical judgement in review of aggregate data and individual cases | Collaborate with CSRM

from: Pharmadiversityjobboard.com - 4 days ago