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IQVIA is hiring a Clinical Research Associate, Sponsor Dedicated to monitor clinical trial sites and ensure study conduct and data reporting comply with protocols, regulations, guidelines, and sponsor requirements.

NextCode Placement is recruiting for a Clinical Research Associate role in New York, NY; the hiring client is not identified.

The hiring employer is not identified in the posting. The FSP Clinical Research Associate monitors clinical trial sites, supports site management and regulatory compliance, and helps ensure participant welfare and data reliability for a sponsor.

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and correc

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processe

Responsibilities Monitors investigator sites with a risk-based monitoring approach Applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into…

Responsibilities Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -…

Moffitt Cancer Center is hiring a Revenue Cycle Systems Analyst II to support accurate and timely billing within the Epic environment.

Responsibilities Collaborate with internal customer/stakeholders to define and document data, analytics, and reporting requirements Assist in the preparation, cleansing, and verification of data Ensure timely completion of data requests, using appropriate…

Cleveland Clinic is hiring a Beaker CPI Systems Analyst I to support and optimize Epic Beaker/LIS applications, specializing in outreach laboratory interfacing and maintenance.

Monitors investigator sites with a risk-based monitoring approach Applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site pro

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial Performs clinical study site management/monitoring activities in compliance

Responsibilities Considered as the primary point of contact for the investigative site. High level of competency or experience in providing contextual information on the clinical trials, connects stakeholder to the investigative sites and strengthens AbbVie’s…

Kelly is hiring on behalf of an unnamed global life sciences client for a six-month clinical research project.

UBC provides pharmaceutical and clinical research services across the drug development and commercialization lifecycle.

AbbVie is hiring a Clinical Research Associate II to advance its clinical research pipeline in oncology. The role partners with investigators and site staff to oversee clinical trial conduct, data integrity, compliance, site performance, and patient safety.

Responsibilities DCT study oversight and management Ensures timely operationalization of each project plan, by setting priorities for each study team member in accordance with project plans, ProPharma Group Standard Operational Procedures (SOPs), ICH/GCP…

Palmetto GBA hires an Analyst, Appeals to research complex appeals and retrospective review requests. The role conducts clinical reviews or benefit analyses to assess medical necessity and documents decisions within required timeframes and in compliance with…

Responsibilities Develop detailed understanding of application functionality by working with senior staff, attending training and/or reading documentation Collaborate with end users to understand and define requirements Use technical and analytical skills to…

Moffitt Cancer Center hires a Clinical Research RN I to coordinate clinical trials and protocol-related care for patients.