Research Site Coordinator

Psi CRO is seeking a highly organized Research Data Coordinator to support our clinical research projects. The successful candidate will be responsible for tracking database set-up, testing, maintenance, and data entry, as well as communicating with clients, project teams, and vendors.Main Responsibilities:Database management and data entryData management...

Job OverviewA Clinical Trial Assistant provides administrative support to the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery. Key responsibilities include:Assisting CRAs and RSU team with updating and maintaining clinical documents and systems.Preparing, handling, distributing,...

Job DescriptionRole Summary:We are looking for a Regulatory Start-Up Specialist to join our team in Argentina. As a Regulatory Start-Up Specialist, you will play a critical role in ensuring that all site activation activities are conducted in accordance with applicable regulations, SOPs, and project requirements.Duties and Responsibilities:Perform site...

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...

Key QualificationsCollege/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience.Participation in clinical projects as a Lead/Senior Monitor.Independent on-site monitoring experience.The ideal candidate will have a strong background in clinical research and possess excellent communication,...

Job DescriptionWe are looking for a seasoned Global Clinical Project Manager to join our team at Innovaderm Research Inc. As a key member of our clinical trials group, you will be responsible for leading multiple projects simultaneously and ensuring timely delivery of high-quality results.Key ResponsibilitiesManage site selection, regulatory affairs, data...

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 an experienced Clinical Research Manager to join our team at Msd. The successful candidate will be responsible for the end-to-end performance of assigned protocols in a country, ensuring compliance with regulations, company policies and procedures, quality standards, and adverse event reporting requirements.The ideal candidate...

At IQVIA, we are committed to delivering innovative solutions in clinical research. As a Clinical Research Associate, you will play a vital role in ensuring the integrity and quality of our studies.The ideal candidate for this position will have experience in therapeutic areas such as Oncology, Cardiovascular, Internal Medicine, and Ophthalmology. This role...

Job OverviewThe Associate Research Analyst role at Latamcent supports the creation, distribution, management, analysis, and reporting of online survey-based research studies, as well as analysis and reporting on customer satisfaction surveys for our clients.About the JobCollaborates with cross-functional teams to design and execute research studies.Analyzes...

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...

Payment Coordination Role:You will contribute to everything from payments administration to the development and enhancement of payment strategies that make a difference.Your Key Responsibilities:Review Investigator Grant budgets against Clinical Study Protocols in cooperation with Project Management DepartmentDevelop country-specific generic site payment...

Job SummaryThe Senior Clinical Research Associate will play a pivotal role in the planning, execution, and management of clinical trials. This position requires an experienced professional who can ensure the integrity of clinical data, compliance with regulatory requirements, and the overall success of clinical research projects.Key ResponsibilitiesPerform...

Job OverviewAs a key member of the clinical research team, the successful candidate will perform daily administrative tasks to ensure the timely and accurate delivery of Trial Master Files. This role requires close collaboration with Clinical Research Associates and Regulatory and Start-Up teams to maintain accurate records and track site compliance.Key...

About IQVIA ArgentinaWe are seeking a highly skilled Regulatory Start-Up Specialist to join our team in Argentina.Responsibilities:As a Regulatory Start-Up Specialist, you will be responsible for ensuring that all site activation activities are conducted in accordance with applicable regulations, SOPs, and project requirements.You will work closely with the...

**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...

About the RoleLilly is a global healthcare leader that unites caring with discovery to make life better for people around the world.Our employees work together to discover and bring life-changing medicines to those who need them, improve disease understanding and management, and give back to our communities through philanthropy and volunteerism.We prioritize...

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 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...

IQVIA Biotech is hiring in Argentina Join our team as a Clinical Research Associate.The ideal candidate will have varied therapeutic experience and be willing to work across multiple therapeutics including: Oncology, Cardiovascular, Internal Medicine, & Ophthalmology.This role will be home-based in Buenos Aires, Argentina.Job Description Summary Perform...