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Responsibilities
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential FunctionsUnder general supervision, serve as Single Point of Contact (SPOC) e Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.Prepare site regulatory documents, reviewing for completeness and accuracy.Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.Review and provide feedback to management on site performance metrics.Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.Inform team members of completion of regulatory and contractual documents for individual sites.Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.Provide local expertise to SAMs and project team during initial and on-going project timeline planning.Perform quality control of documents provided by sites.May have direct contact with sponsors on specific initiatives.QualificationsBachelor's Degree in life sciences or a related field and 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience.3 years clinical research experience, including 1 year experience in a leadership capacity. Equivalent combination of education, training and experience.In-depth knowledge of clinical systems, procedures, and corporate standards.Good negotiating and communication skills with ability to challenge, if applicable.Effective communication, organizational, and interpersonal skills.Ability to work independently and to effectively prioritize tasks.Ability to manage multiple projects.Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards.Understanding of regulated clinical trial environment and knowledge of drug development process.Ability to establish and maintaagers and clients.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comWhere you'll workHome-basedYou’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.CultureCulture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.
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