Empleos actuales relacionados con Associate Project Coordinator - Buenos Aires - Labcorp
-
Clinical Research Project Coordinator
hace 1 semana
Buenos Aires, Argentina Medpace, Inc. A tiempo completoJob Summary: Join Medpace in our Buenos Aires office! We are currently seeking a full-time, office-based **Clinical Research Project Coordinator** to join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your...
-
Junior Project Coordinator
hace 2 semanas
Buenos Aires, Argentina Cognizant A tiempo completo**Junior Project Coordinator**: **Location**: Buenos Aires, Argentina. Hybrid. (Shift flexibility required for EST or CST coverage) **Work Model**: Hybrid, twice a week at office, flexible days. **Shift**: Standard shift, flexibility required for EST or CST coverage. **About the role**: We are seeking a motivated and detail-oriented Junior Project...
-
Project Coordinator
hace 4 días
Buenos Aires, Argentina Cortelco Systems A tiempo completo**SUMMARY OF FUNCTIONS** The Project Coordinator/Manager shall have previous experience in the management of installation of solutions from initial engagement through to fulfillment and Customer’s signature of acceptance. Will act as a focal point between Customer, Account Manager, Customer Support, 3rd party Vendors, Marketing, Sales/Design specialists,...
-
Saas Project Coordinator
hace 7 días
Buenos Aires, Argentina Ailet A tiempo completoWe’re **Ailet**, a leading tech company providing high-tech services to the FMCG/Retail sector using image recognition technologies to boost sales efficiency. Our solutions grant real-time measurements of the most relevant shelf indicators. We help brands to know what’s happening in-store and how to improve sales performances. Ailet is collaborating...
-
Global Marketing Project Coordinator
hace 6 días
Buenos Aires, Argentina UJV A tiempo completoA luxury travel service company is seeking a proactive Marketing Project Coordinator in Buenos Aires. In this role, you will manage marketing projects, coordinate across diverse teams, and ensure timely communication and clarity. Your experience with Asana and Notion will support your efforts in keeping projects on track. Ideal candidates have 2–4 years of...
-
Saas Project Coordinator
hace 4 días
Buenos Aires, Argentina Ailet A tiempo completoWe’re **Ailet**, a leading tech company providing high-tech services to the FMCG/Retail sector using image recognition technologies to boost sales efficiency. Our solutions grant real-time measurements of the most relevant shelf indicators. We help brands to know what’s happening in-store and how to improve sales performances. Ailet is collaborating...
-
Clinical Research Project Coordinator
hace 1 semana
Buenos Aires, Argentina Medpace, Inc. A tiempo completoJob Summary: We are currently seeking a full-time, office-based **Clinical Research Project Coordinator** to join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and...
-
Clinical Research Project Coordinator
hace 3 días
Buenos Aires, Argentina Medpace, Inc. A tiempo completoJob Summary: Join Medpace in our Buenos Aires office! We are currently seeking a full-time, office-based **Clinical Research Project Coordinator** to join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your...
-
Project Associate
hace 12 horas
Buenos Aires, Buenos Aires C.F., Argentina サイネオス・ヘルス A tiempo completoUpdated: December 3, 2025Location: Buenos Aires, B, ArgentinaJob ID: Not ready to apply?Join our Talent NetworkDescriptionProject Associate (Ideal for people with experience with Global studies) English Advance - Hybrid position Buenos Aires ARGSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer...
-
Project Associate
hace 12 horas
Buenos Aires, Buenos Aires C.F., Argentina Syneos Health A tiempo completoDescriptionProject Associate (Ideal for people with experience with Global studies) English Advance - Hybrid position Buenos Aires ARGSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern...
Associate Project Coordinator
hace 3 semanas
Responsible for the coordination and completion of project tasks in support of Project Management for low complex studies.
- Initiates creation of study specific documents (e.g., Project Management Plan, Communication Plan, Risk Mitigation Plan).
- Develops trial management tools to monitor study activity, including project setup activities; formats, posts, and compiles study timelines.
- Attends, schedules, and organizes study-related meetings; distributes agendas, maintains and distributes meeting minutes, Project and Risk Log.
- Works with the document specialist team as appropriate to transfer documents in a timely manner to the Trial Master File (TMF) in accordance with applicable SOPs, policies, system, and client requirements.
- Works with a more senior PC or PM in developing study specific documents (e.g., Project Management Plan, Communication Plan, Investigator Package Plan, Risk Register, Project Specific Training Matrix and any other applicable plans as required), including compliance with client-specific requirements for low complex studies; distributes them to the study team and/or sponsor for review, compiles comments, and routes final documents.
- Works with a more senior PC or PM to monitor training compliance of the study team and update the training matrix as required.
- Maintains an internal standardized filing structure for study-related documents; proactively maintains documents within the filing structure.
- Responsible for project setup activities (e.g., study ID request, SAS Environment Setup request, eTMF, Study-specific Distribution Lists, etc.).
- Assists the PM or a more senior PC in the setup of and updating of CTMS, as required.
- Attends and assists in the organization of study-related meetings, as required; distributes meeting agendas; maintains and distributes meeting minutes, Project Log, Risk Register, and study team contact lists; participates in client visits as needed.
- If required may assist document specialists in document transfer to the Trial Master File (TMF) in accordance with applicable SOPs, policies, system, and client requirements; works with the PM and Document Specialist (DS) to lead eTMF audit readiness efforts and to set up any applicable eTMF QC tools, and may assist in the coordination of eTMF quality reviews.
- Upon request, posts documents such as CRA reports, project deliverables, trackers, regulatory documents, metrics, agendas, and minutes to internal SharePoint/client websites after completing administrator and program training on the required system.
- As directed and with oversight, assists with business improvements initiatives to drive quality, productivity, and continuous improvements across different business units.
- Upon PM request and with Associate Project Coordinator (PC) acceptance, may serve as a sponsor and site contact in the absence of the PM, primarily during maintenance phases of routine single and multi-site low-complexity trials.
- Assists the PM or a more senior PC with payments per global finance standards.
- Assists in the set-up, coordination and maintenance of sponsor/internal training in accordance with applicable SOPs and processes.
- Assists in the development of project tools as required for the project (e.g., screening and enrolment log and development of investigator training).
- May assist the PM or a more senior PC in the set up site regulatory binders (site master file including phannacy file if required).
- Assists the PM, or more senior PC as required with feasibility, including providing sites with feasibility questionnaire and tracking responses.
- May assist the Stat1Up team with tasks including execution of confidentiality agreements, execution of contracts and budgets, collection of regulatory documents and EC I IRB submissions, collating the information from the site into appropriate tracking document.
- May assist the PM or more senior PC with leading external site calls.
- May act as the primary point of contact for external sites during study maintenance, responding to queries, providing documents.
- Assists the PM or a more senior PC in the formatting, posting, compiling and entering budgeted hours into the project timeline.
- Assists the PM/more senior PC in maintaining overall project trackers, including financial, screening, and vendors.
- May work with the PM to assist with work scope changes as they relate to changes in the sponsor contract.
- Performs other duties, as assigned.
**Experience**:
- Knowledge of the clinical trial process with early clinical pharmacology experience preferred.
- Minimum 1-2 years of experience in a research environment.
- Knowledge of protocol designs, study objectives, study procedures, and project-related
time lines.
- Knowledge of GCP/ICH Guidelines and applicable Regulatory Authority Guidelines.
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applican
