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Clinical Trials Site Identification Specialist
2 mesi fa
Overview
PSI CRO is a leading Contract Research Organization with a strong focus on delivering high-quality services across various therapeutic indications. We are seeking a highly skilled Clinical Trials Site Identification Specialist to join our team.
Key Responsibilities
- Start-up Responsibilities:
- Collaborate with internal teams and external stakeholders to identify and evaluate potential clinical trial sites.
- Develop and maintain relationships with medical professionals and site personnel to ensure successful site identification and activation.
- Ensure seamless handovers between teams and stakeholders to ensure project timelines are met.
- Conduct thorough site assessments to identify optimal site profiles and recommend high-quality sites for clinical trials.
- Review and analyze therapeutic indication and study-specific materials to inform site identification strategies.
- Develop and maintain a site identification tracker to monitor progress and identify potential risks or issues.
- Regularly communicate with project teams to update them on site identification status and highlight any potential challenges or opportunities.
- Ongoing Project Responsibilities (all phases):
- Develop and maintain a therapeutic area-specific site database to support site identification and selection.
- Assist project teams during the enrollment phase by identifying additional sites and developing strategies to accelerate site identification.
- Utilize external databases, site networks, and other resources to identify and engage potential clinical trial sites.
- Train and mentor clinical trial associates (CTAs) and clinical research associates (CRAs) on site identification and engagement best practices.
- Participate in the preparation of presentations for client and bid defense meetings, providing input on regulatory aspects as needed.
Qualifications
- Bachelor's degree in a life science or related field (CRA experience is a plus).
- Experience working in healthcare settings (hospital, outpatient clinic) is a strong plus.
- Prior experience in site identification and study start-up activities is a strong plus.
- Practical experience in clinical trials-related activities (study coordinator, sub-investigator) is a strong plus.
- Excellent written and oral communication skills, as well as time management skills.
- Demonstrated ability to multitask under compressed deadlines across multiple projects with unique requirements.
- Advanced English language skills and native Italian language proficiency.
About Us
At PSI CRO, we value excellence, passion, and dedication. We are a dynamic and growing company that prioritizes our people and provides opportunities for growth and development. If you are a motivated and detail-oriented individual with a passion for clinical trials, we encourage you to apply for this exciting opportunity.
