Empleos de study start up manager en buenos aires

Job SummaryOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Buenos Aires! This position plays a key role in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop...

Department: Clinical Trial Operations, International OperationsLocation: Vicente López, Buenos Aires. Hybrid working.Your impact begins hereAs Study Start Up Analyst, you will help clinical trials in Argentina get started on time and the right way. You will prepare and submit the documents that Health Authorities and Ethics Committees need to approve a...

Department: Clinical Trial Operations, International Operations Location: Vicente López, Buenos Aires. Hybrid working. Your impact begins here As Study Start Up Analyst, you will help clinical trials in Argentina get started on time and the right way. You will prepare and submit the documents that Health Authorities and Ethics Committees need to approve a...

Study Start Up Associate II (North America experience - US/Canada))At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the...

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. We are currently seeking a Site Specialist II (Study Start Up Associate II) to join our diverse and dynamic team.As a Site Specialist I at ICON, you will support investigator sites with key administrative...

Clinical Support Specialist | Ideal Opportunity for Regulatory, Study Start-Up & Site Activation Specialists | Argentina Hybrid Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping...

Medpace Buenos Aires is seeking a full-time, office-based Site Contract Manager to join our LatAm Site Contracts team in Clinical Operations. You will report to the LatAm Senior Contract Manager and help drive study start-up and trial management.The role requires LATAM site contract expertise, knowledge of GCP, and English fluency. You will lead...

Job Overview Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start‑up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites, this role ensures smooth progression from feasibility and initial outreach...

IQVIA LLC is seeking a Site Activation Specialist, ICF Lead to operate in LATAM on a remote basis. You will function as a senior individual contributor, coordinating site activation activities and ensuring compliance with local and international regulations, SOPs, and budgets.In this role you will manage feasibility, site identification, regulatory...

Medpace is seeking a full-time Contract Specialist to join the LatAm Site Contract Team within Clinical Operations. The role focuses on study start-up and management of site contracts with investigators and internal teams.You will prepare, negotiate and finalize CDA/CTA documents, budgets and LOI amendments, monitor timelines, and mitigate risks to ensure...

Novo Nordisk is seeking a Study Start Up Analyst for Vicente López, Buenos Aires, with hybrid working. You will own start-up and submission activities for assigned trials, ensuring timely and compliant Health Authority and Ethics Committee dossiers in line with ICH GCP.You will collaborate with Trial Managers and local teams, translate key documents, manage...

Fortrea Argentina S.A. is seeking a Site Navigator II to coordinate site-level activities during the start-up phase of a clinical study.You will act as the single point of contact for investigative sites, ensuring regulatory compliance, training, and effective collaboration among sponsor, CRO, and site staff. Responsibilities include overseeing site...

Assoc. Site Activation Manager (Study Start Up) – Global Study LeadershipAt IQVIA, our Assoc. Site Activation Managers play a critical role in bringing innovative medicines to patients faster. You'll lead global study start-up and site activation activities, partnering with sponsors, investigative sites and cross-functional teams to accelerate patient...

ICON Strategic Solutions is seeking a Study Start Up Associate II for North America experience (US/Canada). You will join a sponsor-dedicated model supported by ICON's global expertise to drive regulatory-compliant study initiation and start-up activities.You will lead site start-up, ensure regulatory submissions are prepared and filed, and collaborate with...

Assoc. Site Activation Manager (Study Start Up) – Global Study Leadership At IQVIA, our Assoc. Site Activation Managers play a critical role in bringing innovative medicines to patients faster. You'll lead global study start-up and site activation activities, partnering with sponsors, investigative sites and cross-functional teams to accelerate patient...

We are seeking Laboratory Project Set-up Manager to join IQVIA Laboratories at Buenos Aires, Argentina. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary: Manage the...

## Clinical Data ManagerApply: Remote: Buenos Aires, Argentina: Virtual Argentina: Full time: Posted Today: JR103087**Who we are**We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take...

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

Job Summary Join Medpace at our Buenos Aires office! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office based Site Contract Manager to join our LatAm Site Contracts team within the Clinical Operations department. This position will report to the LatAm Senior Contract Manager and will play a key role in...

Overview The project manager II has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The project manager II oversees and coordinates study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard...