Empleos de medpace en Buenos Aires

Medpace is the leading CRO for Biotech companies and is continuing to add and established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Buenos Aires, Argentina. Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more. We offer a very competitive salary/bonus...

Join Medpace in our Buenos Aires office! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with Regulatory...

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...

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...

Medpace in Buenos Aires, Argentina is seeking a Clinical Trial Manager to oversee day-to-day project operations, lead cross-functional teams, and ensure high-quality study deliverables in alignment with ICH/GCP. The role emphasizes clinical deliverables and protocol knowledge.The position requires 2–3 years of CRO-PI/CTM experience, English fluency, and a...

Medpace is seeking a Regulatory Submissions Coordinator for our Buenos Aires office to support ethics submissions and regulatory documentation. You will work closely with Regulatory Submissions Coordinators and Start Up teams to help ensure timely delivery of study materials and regulatory compliance.The role requires 1–3 years of regulatory submissions...

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 Summary Our Latin American activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical SafetyCoordinator to join our team! This position plays a key role inthe pharmacovigilanceprocess at Medpace.Working in a team to accomplish tasks and projects that are instrumental to the company’s success.If you want an exciting...

Job Summary Join Medpace in Buenos Aires! The Clinical Research Associate position at Medpace offers a unique opportunity to have an exciting career in the research of drug and medical device development.For those withmedical and/or health/life science interest and backgroundwho want to explore the research field,travel throughout Argentina, and be part of a...

Medpace is seeking a Clinical Research Associate in Buenos Aires to join our research-driven team. This role offers an exciting career in drug and medical device development, with travel across Argentina and entry into Medpace's CRA training program (PACE).No clinical experience may be required for the training pathway, with comprehensive initial and ongoing...

Medpace, Inc. is seeking a full-time, office-based Clinical Safety Coordinator to join our growing LATAM team in Buenos Aires. You will contribute to pharmacovigilance processes and collaborate with global cross-functional partners to ensure safety reporting and compliant documentation.The role requires a life sciences degree, GCP knowledge, and fluency in...

Job SummaryJoin Medpace in our Buenos Aires office! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with...

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Contract Specialist to join our LatAm Site Contract Team within the Clinical Operations team. This position will report to the LatAm Contract Manager and will play a key role in the study start-up and clinical trial management processes at Medpace. The Contract...

Medpace in Buenos Aires is seeking a Regulatory Submissions Coordinator to join our Regulatory Submissions team. You will work on multiple projects and gain experience in regulatory processes while being mentored and supported for career development.You will collaborate with Coordinators to collect essential documents, prepare submissions, and ensure...

Medpace is seeking a Centralized Monitoring Lead for LATAM on a remote basis. The role partners with project and clinical leads to ensure delivery aligns with contract objectives, while optimizing speed, quality and cost in accordance with IQVIA SOPs and practices.The role requires a life sciences degree, 3+ years of clinical monitoring experience (remote or...

Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Contract Specialist to join our LatAm Site Contract Team within the Clinical Operations team. This position will report to the LatAm Contract Manager and will play a key role in the study start-up and clinical trial management processes at Medpace....

Medpace is seeking a full-time Contract Specialist to join the LatAm Site Contract Team within Clinical Operations. The role supports study start-up and site contract management, reporting to the LatAm Contract Manager, and advancing project start-up activities.The ideal candidate has 2–4 years of site contract negotiation experience, a relevant...

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...

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...

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...