Helping life science innovators turn breakthrough science into life-changing drugs, devices, and diagnostics.
Morrisville, NC
Premier Research International LLC (Premier) is a global leader in clinical research and consulting services with expertise in driving an efficient and effective path to market for the life sciences industry. Premier is built with the needs of biotech in mind, turning breakthrough science into life-changing drugs, devices, and diagnostics by addressing trial complexity, overcoming development hurdles, and demonstrating product value. Leveraging deep therapeutic expertise, innovative technology, and product development operational proficiency—from preclinical planning to clinical trial execution and commercialization—our integrated approach offers personalized, end-to-end solutions to identify the pertinent data and insight necessary to make informed decisions earlier and deliver accelerated development timelines for a smarter, faster path to approval. Through our commitment to partner boldly, deliver impact, and foster community, we’re driving change that advances research and improves lives while creating meaningful opportunity for patients, customers, and all Premier team members. Follow our page to learn more about our work—and explore career opportunities to be part of the transformation.
Remote · Quebec, Quebec, Canada
Perform clinical monitoring activities including site qualification, initiation, and close-out visits for various clinical trials. Manage investigative sites, ensure data integrity and patient safety, and maintain accurate documentation in accordance with study protocols.
Remote · Canada
The Site Start up Associate II manages clinical trial start-up timelines, including regulatory submissions and site-specific contract and budget negotiations. They ensure compliance with local regulations and ICH/GCP guidelines while serving as a primary point of contact for project stakeholders.
Remote · Ontario, Canada, Quebec, Quebec, Canada
The Senior Clinical Research Associate will conduct source verification, manage site documentation, and resolve data discrepancies to ensure compliance with protocols. They will also handle budget negotiations with clinical trial sites and maintain thorough documentation of all study activities.
Remote · United States
Serve as the initial contact for site management and monitoring quality concerns, oversee clinical monitoring and site management deliverables, and contribute to the central monitoring plan. Track clinical operations metrics and timelines, support audit readiness and remediation, represent Clinical and SSU in sponsor calls, and escalate performance or quality concerns and reportable events.
Remote · United States
Manage and coordinate global project teams across Regulatory, Clinical Operations, and Medical Affairs to ensure milestone achievement and project delivery. Act as the primary liaison for customers while managing project budgets, scope, and business development activities.
