Trial Capabilities Associate Jr

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our...

Our MissionTFS HealthScience specializes in providing flexible clinical development and strategic resourcing solutions across key therapeutic areas, including Dermatology, Neuroscience, Oncology, and Ophthalmology.As a Senior Clinical Research Associate, you will be responsible for overseeing clinical trials to ensure their quality, integrity, and progress....

At TFS HealthScience, we are dedicated to advancing clinical research through innovative solutions and a commitment to quality. We provide tailored services across the clinical development lifecycle to deliver impactful results for our clients and the healthcare industry.Role Overview:We are looking for a Clinical Trial Associate to support TMF archiving and...

TFS HealthScience is a global Contract Research Organization with a strong commitment to delivering high-quality services in the clinical development lifecycle.Clinical Trial Associate Role OverviewWe are seeking a skilled Clinical Trial Associate to support TMF archiving and documentation activities on-site, ensuring regulatory compliance and readiness for...

Local Trial Management services provides local management of a clinical trial (or Medical Affairs data generation activity) in the country. Services/deliverables include operational oversight of assigned protocol(s) at the country level from start-up through to database lock and closeout activities. Further, services will ensure the local trial team is...

TFS HealthScience is a global leader in contract research services, dedicated to advancing human health through innovative partnerships.We are seeking a highly skilled Senior Clinical Research Associate to join our team in Lisbon, Portugal.About the OpportunityAs a Senior Clinical Research Associate with TFS HealthScience, you will contribute to the success...

**Join us as a **Clinical Trials Assistant!**: **What You´ll Do** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up...

100,000. That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations (GCO) touches patients’ lives every day acting as a link between science and medicine. Envision the impact you could have! #GCO The Clinical Trial Associate (CTA) supports SSO Study Start-Up Manager and SSO Clinical Project Manager in...

**Job Overview** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...

Join us as a Clinical Trials Assistant! - What You´ll DoPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with...

Job SummaryWe are seeking a highly skilled Regulatory Submissions Manager to join our Study Start Up team in Buenos Aires.This role plays a key part in the clinical trial management process at Medpace.The successful candidate will have at least 4 years of experience in regulatory submissions/start-up management and knowledge of Clinical Trial Applications...

Job Summary: 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...

External Job Description **Job Overview** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately...

**Are you a brave mind?** It takes insight, curiosity, and intellectual courage to transform healthcare. It takes brave minds. By reimagining a world without the consequences of disease, brave minds bring powerful ideas to reality. Not intimidated by complexity, they see possibilities and explore the improbable. **Join us as a **Clinical Trials...

**Senior Clinical Associate - Buenos Aires, Argentina** 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...