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ICON is a global healthcare intelligence and clinical research organisation focused on bringing new medicines and treatments to patients faster. The Clinical Research Associate II serves as the primary contact between investigational sites and the sponsor, conducting site monitoring visits, ensuring compliance, supporting patient safety and recruitment, and maintaining high-quality clinical trial data and documentati

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 positioning Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program, protocol and patient treatment pr

Responsibilities Responsibilities may differ slightly from the above based on specific needs of the business Develop strong site relationships and ensures continuity of site relationships through all phases of the trial Performs, with oversight, clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documen

ICON Strategic Solutions provides sponsor-dedicated clinical research services supported by global expertise. The Clinical Research Associate II will serve as the primary liaison between investigational sites and the sponsor, conduct site monitoring visits, ensure regulatory and protocol compliance, support patient safety and recruitment, and manage clinical documentation and data quality. Responsibilities Serve as t

Responsibilities Serves as the primary contact for assigned investigational sites and develops effective working relationships with investigators and site staff Schedules and independently conducts monitoring activities, both on-site and remotely, including pre-study/site qualification, site initiation, interim monitoring, and close-out visits, in accordance with study protocols, Monitoring Plans, Company and/or clie

Responsibilities Act as the main line of communication between the project team, sponsor, and the site Build and maintain a good relationship with the site staff involved in the study conduct Prepare, conduct, and report site selection, initiation, routine monitoring and close-out visits Ensure that subject recruitment targets are timely defined, communicated, recorded and met, and project timelines are followed at s

Responsibilities Act as the main line of communication between the project team, sponsor, and the site Build and maintain a good relationship with the site staff involved in the study conduct Prepare, conduct, and report site selection, initiation, routine monitoring and close-out visits Ensure that subject recruitment targets are timely defined, communicated, recorded and met, and project timelines are followed at s

ICON plc is a global healthcare intelligence and clinical research organisation focused on bringing new medicines and treatments to patients faster. The Clinical Research Associate II supports clinical trials by conducting site visits, ensuring protocol compliance and patient safety, collaborating with investigators, reviewing clinical data, and contributing to study documentation. Responsibilities Conducting site qu

Emmes Group is a clinical research organization and technology company focused on advancing healthcare through clinical research, data, and analytical solutions. The Clinical Research Associate II monitors clinical study sites remotely and onsite, ensuring trials comply with protocols, SOPs, ICH GCP, and applicable regulations. The role also conducts monitoring visits, documents findings, supports site staff, resolve

BrioHealth Solutions is a med-tech company developing patient-centric heart failure therapies, including the BrioVAD Left Ventricular Assist System. The Clinical Research Associate II will support clinical trial execution by monitoring sites, ensuring data integrity and protocol compliance, managing regulatory submissions and trial supplies, and maintaining clinical systems throughout the study lifecycle. Responsibil

RQM+ is a MedTech contract research organization providing regulatory, quality, laboratory, clinical trial, and reimbursement services. The Clinical Research Associate II participates in preparing and executing pre-market through post-market clinical trials, conducting site visits and monitoring investigations in accordance with Good Clinical Practices. The role also coordinates regulatory documentation, clinical dat

RQM+ is a MedTech contract research organization providing regulatory, quality, laboratory, clinical trial, and reimbursement services for medical technologies. The Clinical Research Associate II supports pre-market through post-market clinical trials by coordinating site activities, conducting monitoring visits, ensuring regulatory and Good Clinical Practice compliance, reviewing clinical data, and supporting study

Responsibilities Independently perform full-scope remote and on-site monitoring visits involving source document verification, review of essential regulatory documents, and assessing site performance Ensure compliance with clinical trial protocols based on regulations, ICH GCP guidelines, and NMDP standard operations procedures Identify and communicate site findings with site study personnel and the study team Perfor