Site Selection Specialist

This is a fully remote position, open to applicants in Argentina.

📋 Description

• Act as the primary contact for site selection processes, which encompass site identification and feasibility assessments.

• Cultivate and sustain effective relationships with prominent clinical research sites.

• Identify researchers and research facilities through literature reviews and online investigations.

• Gather data to characterize ideal investigators for various studies.

• Identify and propose potential investigators.

• Design and implement interest survey assessments.

• Develop and manage study-specific feasibility questionnaires.

• Evaluate feasibility questionnaires and suggest sites for qualification visits.

• Oversee CRA resource distribution for site qualification visits.

• Analyze summaries from site qualification visits.

• Recommend sites for study involvement in collaboration with sponsors and project teams.

• Monitor site selection activities within the Clinical Trial Management System (CTMS).

• Participate in necessary internal and external project team meetings.

• Detect site performance quality issues via project meetings, escalated communications, and quality assurance audit findings.

• Engage in internal departmental projects and provide expertise in site selection and site intelligence.

• Assist the Manager of Site Selection in achieving high-quality project outcomes.

⛳️ Requirements

• Bachelor’s degree in a scientific or related field.

• Strong verbal and written communication skills in English; proficiency in French is a plus.

• At least 3 years of experience in clinical research within the biotechnology, pharmaceutical, or CRO sectors.

• Extensive and relevant background in site selection, study initiation activities, site budget/contract negotiations, and/or close collaboration with sites or within a site setting.

• Proficient with Microsoft Office applications (Word, Excel, PowerPoint).

• Experience in dermatological clinical research is advantageous.

• Quick learner with strong adaptability and versatility.

• Capability to work collaboratively in a team and build solid relationships with colleagues, sponsors, and sites.

• Well-organized and capable of managing competing priorities in a dynamic, fast-paced environment.

• Flexible, with a positive attitude, exceptional attention to detail, and strong critical thinking abilities.

• Good understanding of Good Clinical Practices and relevant Health Canada and FDA regulations/guidelines.

• Must possess legal eligibility to work in Argentina.

🏝️ Benefits

• Flexible working hours.

• Position allows for remote work.

• Continuous learning and professional development opportunities.

• Attractive prospects for career advancement.

• Commitment to fair treatment and equal opportunities.

• Accommodations in recruitment and selection for applicants with disabilities, available upon request.