Clinical Trials Site Manager
7 days ago
Site Management Expert
">We are seeking a skilled Site Care Partner to join our team. As a Site Care Partner, you will be responsible for managing the day-to-day activities of sites involved in clinical trials. Your primary goal will be to ensure that these sites operate efficiently and effectively, providing high-quality data and support to the research process.
">Your key responsibilities will include:
">- ">
- Qualify and Activate Sites: You will identify and qualify potential sites for clinical trials, assessing their suitability and feasibility. Once qualified, you will activate these sites, ensuring they meet all necessary requirements.">
- Optimize Country & Site Selection: You will collaborate with stakeholders to optimize country and site selection processes, reviewing draft lists and providing Pre-Trial Assessment (PTA) output to support informed decisions.">
- Maintain Protocol Knowledge: You will stay up-to-date with assigned protocols, ensuring your knowledge is current and relevant to the research being conducted.">
- Conduct Study Start-up Activities: You will lead study start-up activities at the site level, including PTA, coordination of site activation checklist items, Informed Consent Document (ICD) finalization, and Site Initiation Visit (SIV).">
- Ensure Site Readiness: You will guarantee that all site initiation activities, including training and documentation collection, are completed accurately and on time.">
- Partner with CRA: You will collaborate with Clinical Research Associates (CRA) to ensure site monitoring readiness for First Subject First Visit (FSFV). Together, you will resolve any issues or challenges that may impact the trial's success.">
- Establish Relationships: You will build and maintain strong relationships with site organizations and strategic partners, fostering trust and cooperation essential for successful trial conduct.">
This role requires:
">- ">
- Experience in Site Management: A minimum of 5 years' experience in site management, preferably with prior experience as a Clinical Research Associate (CRA), is essential for this position.">
- Knowledge of GCP Regulations: A thorough understanding of Good Clinical Practice (GCP) regulations and guidelines is required to ensure compliance with industry standards.">
- Strong Communication Skills: Excellent verbal and written communication skills are crucial for effective collaboration with stakeholders, investigators, and other teams.">
What We Offer
">We provide a stimulating work environment that promotes professional growth and development. Our organization values innovation, teamwork, and dedication to delivering exceptional results.
">About Us
">We are a leading company in the clinical trials industry, committed to advancing medical research and improving human health. Our global presence enables us to partner with researchers, healthcare professionals, and organizations worldwide.
">Benefits
">We offer a comprehensive benefits package, including competitive compensation, opportunities for career advancement, and a supportive work environment that fosters personal and professional growth.
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