CANADA - REMOTE - Global Site Identification & Feasibility Specialist

Job Summary The Global Site Identification and Feasibility Specialist supports the administration of the clinical systems and tools utilized by Development Operations. Works in close collaboration with Development Operations teams, study start-up and/or CROs to provide key inputs, metrics, and outputs to support the selection of the most suitable sites for our clinical studies. Summary of the Essential Functions of the Job Work with clinical study teams to ensure the accuracy of data in CTMS Provide support, under the direction of the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility Specialist, to clinical systems end users, including receipt, evaluation and recommendation for all issue/enhancement requests Conduct research and data analysis to identify potential sites that meet the study criteria and objectives Assist with feasibility launch to include system set-up, feasibility questionnaire creation and site-level feasibility questionnaire outreach Effectively communicating with study teams and relevant stakeholders as needed to coordinate and support additional feasibility activities as identified by the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility Specialist Tracking and data entry of feasibility responses and reporting responses to the internal stakeholders Troubleshoot any issues or discrepancies that arise in the feasibility process (in-house and/or outsourced studies) Stay up to date with current regulations and industry trends related to site feasibility Supporting enrollment forecasting and discussing scenarios with internal or external stakeholders under the supervision of the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility Specialist Minimum Requirements B.S. in a scientific or allied health field (or equivalent degree) and 3+ years of experience demonstrating thorough understanding of clinical trial conduct and processes and/or 2+ years of feasibility/recruitment Experience with trial optimization vendors, tools, and methods Analytical thinker with great attention to detail Good knowledge of concepts of clinical research and drug development Experience collaborating with internal and external stakeholders Ability to prioritize multiple projects and tasks within tight timelines Excellent written and verbal communication skills Demonstrated administrative and project management abilities in an academic, CRO or sponsor environment Experience working in multiple rare disease therapeutic areas Experience with data analysis and interpretation Highly proficient with excel Full-time employees are also eligible for benefits options such as health coverage, life insurance, disability insurance, and 401k benefits. At Advanced Group, our commitment to diversity and inclusion in every part of our organization is crucial to fulfilling our mission and demonstrating our REAL values. Advanced Group is committed to providing employment opportunities without regard to sex, race, color, age, national origin, religion, gender identity or expression, sexual orientation or sexual preference, pregnancy or maternity, genetic information, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law. Advanced Group complies with federal and state disability laws and makes reasonable accommodations for applicants and candidates with disabilities. If a reasonable accommodation is needed to participate in the job application or interview process, please contact View email address on click.appcast.io. #J-18808-Ljbffr Advanced Clinical