Regulatory and Site Activation Leader

**Job Overview**We are seeking a seasoned professional to oversee the delivery of site activation and maintenance activities for selected studies or multi-protocol programs.Key Responsibilities:Develop and implement site activation strategies in accordance with project scope and timelines.Manage site activation teams to ensure timely and within-budget...

Site Activation and MaintenanceThe successful candidate will develop and implement site activation strategies in accordance with project scope and timelines. They will manage site activation teams, collaborate with clients and regulatory specialists, and ensure timely and within-budget delivery of sites.Benefits and Opportunities:Promote innovation and best...

Job Summary:We are seeking a skilled Study Startup Specialist to join our team in Latam. The successful candidate will have a strong background in study and site startup processes in Latin America and excellent communication and organizational skills.Key Responsibilities:Support site identification and selection processCollect, review, and submit documents...

We are seeking an experienced Site Activation and Maintenance Manager - LATAM Regional Expert to join our team at Iqvia Argentina. As a key member of our organization, you will be responsible for leading the development and implementation of site activation and maintenance strategies for our clients across Latin America.Main Responsibilities:Develop and...

ICON plc is a world-leading healthcare intelligence and clinical research organisation.From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.With our patients at the centre of all that we do, we help to accelerate the development of...

**Job Overview**Iqvia Argentina seeks a highly skilled Sponsor Dedicated Manager - Regulatory Expert to lead the delivery of site activation and maintenance activities for selected studies or multi-protocol programs. As a key member of our team, you will be responsible for overseeing the execution of site activation and maintenance strategies, ensuring...

Job SummaryThis Regional Activation Director position involves leading the delivery of site activation and maintenance activities for selected studies or multi-protocol programs in LATAM. You will be responsible for developing and overseeing the implementation of site activation strategies to ensure timely and within-budget delivery of site activation and...

About the RoleThis exciting opportunity is for a Clinical Trial Coordinator - Regulatory Expertise to join our dynamic team. The successful candidate will work closely with cross-functional teams to ensure regulatory compliance and contribute to the development of innovative biopharmaceutical solutions.ResponsibilitiesAssist in the identification and...

Job OverviewSyneos Health is a leading provider of biopharmaceutical solutions, dedicated to accelerating customer success through clinical, medical affairs, and commercial insights.We are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory department, you will be responsible for ensuring compliance with...

Reg & Start Up Manager – Sponsor Dedicated Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work and resources.You will: Oversee the execution of Site Activation and Maintenance for assigned...

ResponsibilitiesPrepare investigator sites to conduct clinical trials through review and approval of essential clinical trial and regulatory documents.Establish site activation timelines with selected sites and coordinate activities to meet planned activation timelines.Communicate with clinical sites during site start-up and collaborate with other functional...

(Assoc) Reg & Start Up Manager - Sponsor DedicatedApply locationsBuenos Aires, ArgentinaSão Paulo, BrazilTime type: Full timePosted on: Posted 3 Days AgoJob requisition ID: R1461659Reg & Start Up Manager – Sponsor Dedicated Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or...

Role Overview: We are seeking a highly experienced Study Operations Coordinator to support our project teams in Argentina. The ideal candidate will have excellent project management skills, a strong understanding of ICH GCP and local regulations, and experience in mentoring and leadership.Key Responsibilities:Oversee and coordinate processes critical for...

About the Role: We are seeking a highly motivated and organized individual to oversee the activation of clinical trial sites in Argentina. The ideal candidate will have excellent communication and project management skills, with a strong understanding of ICH GCP and local regulations.Key Responsibilities:Coordinate site identification and selection...

About Our CompanyWe are a dynamic company that cares about its people and invests in their professional development and success. We are looking for a talented individual to join our clinical operations team in Argentina.Job DescriptionThis role will be responsible for overseeing and coordinating the processes critical for clinical trial sites activation,...

Job Summary: We are looking for a skilled Site Startup Specialist to support our project teams in Argentina. The successful candidate will have experience in clinical research, excellent communication skills, and a strong understanding of local regulations.Responsibilities:Oversee and coordinate processes critical for clinical trial sites...

The Project Coordinator works with Project Managers, Clinical Trial Managers, Site Selection Team and Clinical Research Associates (CRA) to provide administrative and coordinating support for site activation activities and other site level deliverables through all phases of the clinical trial lifecycle.As a Project Coordinator, you will take the lead to...

About UsTrocafone is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.We pride ourselves on our amazing company culture, where we work as one team to...

About Psi CroWe are a global company that brings together passionate individuals to work on the frontline of medical science. We are committed to changing lives and bringing new medicines to those who need them.Job SummaryThis is an exciting opportunity for a highly motivated individual to join our clinical operations team in Argentina as a Study Start-Up...

Job Title: Regulatory Affairs AnalystNovo Nordisk A/S is a global leader in the development and manufacturing of innovative pharmaceuticals. We are currently seeking a talented Regulatory Affairs Analyst to join our team in Argentina.About the RoleThis is an exciting opportunity to work in a dynamic and professional environment where you will be responsible...