Empleos de medpace en Buenos Aires

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....

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 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 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...

Medpace, Inc. in Buenos Aires is seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in LATAM. The role focuses on managing global start-up activities, regulatory submissions, and ensuring quality of essential documents.The ideal candidate has at least 4 years of regulatory submissions/start-up management...

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...

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...

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, 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...

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 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...

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...