[Skip to main content](#main-content) [OpenNash Jobs](https://jobs.opennash.com/) [Hiring report](/reports/hiring/) · [All IQVIA jobs](https://jobs.opennash.com/companies/iqvia/) · [Search jobs](/search/) IQVIA · São Paulo, Brazil # Sr. Site Activation Specialist São Paulo, Brazil Full-time Senior individual contributor Listed on IQVIA’s official careers site. Posted October 14, 2026. Check that it is still open and apply there. [Apply on IQVIA’s careers site →](https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/So-Paulo-Brazil/Sr-Site-Activation-Specialist_R1567108) [OpenNash Jobs](https://jobs.opennash.com/) / [IQVIA](https://jobs.opennash.com/companies/iqvia/) / Sr. Site Activation Specialist ## Job description ### Job Overview 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 activitie. Developing professional individual contributor who works under moderate oversight and supervision. Responsible for making recommendations for enhancements in systems and processes to solve problems or improve effectiveness of job area. Problems faced are general and may require understanding of broader set of issues but are not complex. ### Essential Functions - Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site 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 feasibility, site ID, 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 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 fesibility, site ID, regulatory and contractual documents for individual sites. - Review, track and follow up the progress, the approval and execution of documents, questionnaires, CDA/SIF, 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. ### Qualifications - Bachelor's Degree Life science or related field ### Req And - Other 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. ### Req - 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.com](https://jobs.iqvia.com) IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. ## At a glance - Posted by the employer: Oct 14, 2026 - First seen by OpenNash: Oct 17, 2026 - Last checked: Oct 17, 2026 - Listed for: 3 days - Location: São Paulo, Brazil - Employment type: Full-time[Apply on IQVIA’s careers site →](https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/So-Paulo-Brazil/Sr-Site-Activation-Specialist_R1567108) ## More jobs at IQVIA ### [Analista de Folha de Pagamento e Contabilidade](https://jobs.opennash.com/companies/iqvia/jobs/11511d85c1abb24599f9/) São Paulo, Brazil ### [CRA 2](https://jobs.opennash.com/companies/iqvia/jobs/417aa68aba83f3a28666/) São Paulo, Brazil ### [CRA 2, Brazil](https://jobs.opennash.com/companies/iqvia/jobs/855bf6a391f19613db1f/) São Paulo, Brazil ### [Engenheiro de Dados](https://jobs.opennash.com/companies/iqvia/jobs/8299037a79a783cebf78/) São Paulo, Brazil ### [Especialista de IM/SFE](https://jobs.opennash.com/companies/iqvia/jobs/c88a443012775a1298bd/) São Paulo, Brazil ## Similar jobs at other companies ### [Site Activation Lead](https://jobs.opennash.com/companies/leidos/jobs/64f65d355f523fca8c69/) Leidos ### [Activation GTM Director-Security](https://jobs.opennash.com/companies/microsoft/jobs/80c488b68d08fe8a8c6f/) Microsoft · Singapore ### [Services Activation GTMM - ASEAN](https://jobs.opennash.com/companies/microsoft/jobs/c920450809090136a06e/) Microsoft · Singapore ### [client insights activation manager](https://jobs.opennash.com/companies/richemont/jobs/17ff0a1114f2d9e35a7b/) Richemont ### [clients activation manager hkmo](https://jobs.opennash.com/companies/richemont/jobs/dddd25b7df47b186611b/) Richemont OpenNash lists jobs from employers’ own careers sites and does not handle applications. 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