In this role, you will be responsible for Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials.
In this role, the selected candidate will assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
In this role, the candidate will work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are completed.
In this role, you will assist with all aspects of protocol management, including screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files.
The Coordinator is responsible for supporting the EVP Creative Strategy and Research in all aspects of worldwide market research, traditional and digital media, consumer analytics and marketing strategies. Will assist in strategy and research projects.
In this role, the selected candidate will manage processes to achieve 100% completion rates and timely data collection; train and oversee a team of research analysts responsible for collecting data from new home developments.