Clinical Trials Associate Jobs in Bridgewater, NJ

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 - 12 days ago

Johnson and Johnson - Raritan, NJ

program. The Associate Director, Clinical Project Scientist provides active scientific contribution to a cross-functional clinical team developing a molecular entity. The Associate Director, Clinical

from: Johnson and Johnson - 7 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 - 23 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) - 2 days ago

Johnson & Johnson - Raritan, NJ

. The LDM ensures clinical trial data collected meet the highest standards of data integrity while meeting timelines. Primary Responsibilities: Mentor and train junior associates as needed in clinical data USD 105,000.00 - 150,000.00 per year

from: Dice.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 - 15 days ago

Regeneron Pharmaceuticals - Basking Ridge, New Jersey

, NJ or Uxbridge, England._ The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may

from: HealtheCareers.com - 14 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 - 3 days ago

Abbvie - Madison, NJ

participates in the development of data and reporting standards in support of AbbVie's portfolio of clinical trials and ensuring AbbVie's conformance to CDISC standards and industry best practices. This role

from: Dice.com - 17 days ago

Merck - Rahway, NJ 07065

Job Description Position Description: This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director (CRD) or Head of Site Management

from: Pharmadiversityjobboard.com - 27 days ago