Full-Time Site Identification Specialist

Responsibilities:

• Maintain and generate relations with Investigative Sites.
• Maintain and refine internal site database (with Study Startup, Clinical Operations, and Process Improvement).
• Develop improvement strategies for the site identification process.
• Create initial list of potential sites.
• Communicate with project teams to define strategy and methodology of site contacts.
• Maintain study site identification tracker.
• Evaluate site identification status/progress, highlight potential risks/issues to timelines/objectives.
• Perform due diligence check of regulatory limitations for investigators/clinical sites.
• Participate in project team meetings (as needed).
• Support project team throughout study startup and beyond.

Qualifications:

• University/college degree (life sciences/healthcare preferred) or equivalent.
• Experience in site identification, site management, CRA activities, and/or study startup preferred.
• Knowledge of Good Clinical Practice, local laws, and applicable regulations preferred.
• Full working proficiency in English.
• Strong written/oral communication, time management, organizational, attention-to-detail, and interpersonal skills required.

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