SITE FEASIBILITY SPECIALIST II

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.

Job Overview

Responsible for activities that support the clinical trial process from start-up to close out. Clinical Operation professionals are tasked with the planning, implementation, management, and execution of the clinical trial process.

Long Description
• Identify, contact, and build relationships with study investigators/sites and networks in assigned areas (e.g., region, countries, or therapeutic area) for the conduct of feasibility and potential study participation• Build investigator database and feasibility management system (e.g., investigator profiles, country demographics)• Creates/Coordinate the development of the feasibility questionnaire for a study. Reviews the protocol, seeks expertise from applicable supporting functions (feasibility manger, PM, etc.), and finalizes draft for Sponsor review, as required. Works with PM to obtain client approval of the study specific feasibility questionnaire, as needed.• Create and disseminate Confidential Disclosure Agreements (CDAs)/Questionnaires to sites and follow up accordingly to ascertain interest and to meet study timelines.• Adheres to study timelines, documents, and communicates updates to Project Managers.• Liaise with the project manager to understand studies' budgets and negationists and finalizes budgets with the investigational sites• Responsible for transitioning sites from Site Feasibility to SSU (Study Start Up) representative.• Conduct site qualification visits (on-site and remotely)

What your background should look like:
• Bachelor's degree (or equivalent) in science-related field preferred• 2-3 years relevant experience in clinical research, monitoring or study start up• Equivalent combination of education, training, and experience

Competencies

SET : Strategy, Execution, Talent (for managers)