Empleos actuales relacionados con Senior Site Manager - Buenos Aires - Johnson & Johnson

  • Site Manager

    hace 2 semanas

    Buenos Aires, Argentina Johnson & Johnson A tiempo completo

    At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity. Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130...

  • Clinical Trial Site Manager Senior

    hace 7 días

    Buenos Aires, Buenos Aires C.F., Argentina Dev-Pro A tiempo completo

    Job DescriptionKey ResponsibilitiesServe as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary, ensuring adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables, and project...

  • Assoc Prime Site Manager

    hace 2 días

    Buenos Aires, Argentina IQVIA A tiempo completo

    **Job Overview** Works under moderate supervision to build and maintain partnerships at IQVIA Prime and partner sites to streamline startup processes, maximize the recruitment of patients into trials whilst adhering to high quality standards and improving the experience of patients, site staff and customers working with IQVIA. In liaison with key...

  • Site Id And Feasibility

    hace 2 semanas

    Buenos Aires, Buenos Aires C.F., Argentina Iqvia A tiempo completo

    Job SummaryThe Global Site Identification and Feasibility specialist supports the administration of the clinical systems and tools utilized by Development Operations.Works in close collaboration with Development Operations teams, study start-up and/or CROs to provide key inputs, metrics, and outputs to support the selection of the most suitable sites for our...

  • Site Activation Manager Lead

    hace 7 días

    Buenos Aires, Buenos Aires C.F., Argentina SAP A tiempo completo

    Job SummaryWe are seeking a talented Global Site Activation Specialist to join our Clinical Operations team. As a key member of our team, you will be responsible for performing site activation activities in accordance with applicable regulations, SOPs, and project requirements.Key ResponsibilitiesServe as the Single Point of Contact (SPOC) in assigned...

  • North America Site Activation Manager

    hace 2 semanas

    Buenos Aires, Buenos Aires C.F., Argentina Iqvia Llc A tiempo completo

    Job OverviewAs a Sr Site Activation Coordinator for North America, you will perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual guidelines.You may also be involved in feasibility or...

  • Site Operations Manager

    hace 1 semana

    Buenos Aires, Buenos Aires C.F., Argentina Compass Group Pty Limited A tiempo completo

    **About Us**Compass Group Pty Limited is a leading provider of food and support services. We operate in a variety of environments, including mining sites.**The Role**We are seeking an experienced Site Operations Manager to lead our deep catering team at Southflank minesite.**Key Responsibilities**Lead and manage the daily cleaning operations and stock...

  • Site ID and Feasibility

    hace 3 semanas

    Buenos Aires, Buenos Aires C.F., Argentina IQVIA A tiempo completo

    Job SummaryThe Global Site Identification and Feasibility specialist supports the administration of the clinical systems and tools utilized by Development Operations. Works in close collaboration with Development Operations teams, study start-up and/or CROs to provide key inputs, metrics, and outputs to support the selection of the most suitable sites for...

  • Site ID and Feasibility

    hace 5 días

    Buenos Aires, Buenos Aires C.F., Argentina IQVIA Argentina A tiempo completo

    Job SummaryThe Global Site Identification and Feasibility specialist supports the administration of the clinical systems and tools utilized by Development Operations. Works in close collaboration with Development Operations teams, study start-up and/or CROs to provide key inputs, metrics, and outputs to support the selection of the most suitable sites for...

  • Senior Site Enablement Professional

    hace 2 semanas

    Buenos Aires, Buenos Aires C.F., Argentina Sap A tiempo completo

    About the RoleAs a Sr. Site Activation Specialist, you will play a critical role in ensuring the successful execution of site activation activities in Argentina. You will work closely with the site activation manager, project management team, and other departments to ensure that all necessary steps are taken to activate sites efficiently and effectively.Your...

  • Clinical Project Manager

    hace 7 días

    Buenos Aires, Buenos Aires C.F., Argentina Citi A tiempo completo

    As a key member of our team, we're looking for a skilled Clinical Project Manager to join our team. As a Senior CRA II, you'll be responsible for site management and monitoring for clinical studies. Your expertise will ensure the successful execution of our projects, adhering to Covance Standard Operating Procedures and Regulatory Guidelines.\Key...

  • Senior Site Activation Manager

    hace 2 semanas

    Buenos Aires, Buenos Aires C.F., Argentina Mvl Consulting A tiempo completo

    Job DescriptionCompany OverviewMvl Consulting is a leading consulting firm that provides expert solutions to clients in various industries. We are committed to delivering high-quality services and building long-lasting relationships with our clients.Job SummaryWe are seeking an experienced Sr. Site Activation Specialist In Argentina to join our team. As a...

  • Senior Site Monitor

    hace 7 días

    Buenos Aires, Buenos Aires C.F., Argentina Hopper A tiempo completo

    Job DescriptionThe Senior Clinical Research Associate will serve as the main contact for assigned study sites, conducting site visits and completing deliverables within given timelines.This role involves collecting and reviewing essential documents, participating in investigator meetings, and ensuring proper storage and dispensation of Investigational...

  • Site Activation Project Manager

    hace 5 horas

    Buenos Aires, Buenos Aires C.F., Argentina beBee Careers A tiempo completo

    Job DescriptionThe Site Activation Specialist is responsible for performing site activation activities at a country level in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements, and contractual guidelines. This role may also include maintenance activities.Essential FunctionsServe as...

  • Senior Trial Operations Manager

    hace 1 semana

    Buenos Aires, Buenos Aires C.F., Argentina Citi A tiempo completo

    Role SummaryThe Senior Trial Operations Manager II (STOM II) plays a pivotal role in ensuring the successful execution of clinical trials within assigned countries. This individual serves as the primary point of contact for local trial management, overseeing operational activities from start-up to database lock and closeout.Key Responsibilities:Protocol...

  • Manager, Site Analytics

    hace 17 horas

    Buenos Aires, Argentina Novasyte A tiempo completo

    Join us as a Manager of Site Analytics! What You´ll Do We are looking for a creative analytical mind and an expert in clinical development to take on tough challenges that ultimately make a difference in the lives of patients around the world! If Human Data Science sounds intriguing to you, you need to join our team! You will partner with our clinical...

  • Senior Site Activation Specialist

    hace 10 horas

    Buenos Aires, Buenos Aires C.F., Argentina Dev-Pro A tiempo completo

    Job OverviewAt Dev-Pro, we seek a highly skilled Clinical Research Coordinator - Site Activation to join our team. As a key member of our site activation process, you will be responsible for ensuring the seamless execution of site activation activities across various studies. Your expertise in clinical research and regulatory tasks will be instrumental in...

  • Sr. Site Contracts Associate/site Contracts

    hace 17 horas

    Buenos Aires, Argentina IQVIA A tiempo completo

    External Job Description IQVIA Biotech is seeking a Senior Site Contracts Associate or Site Contracts Associate located in Argentina: **BASIC FUNCTION**: To manage the review and negotiation of contracts with Investigators participating in clinical research on behalf of pharmaceutical Sponsors. **ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES**: -...

  • Senior Site Activation Specialist

    hace 1 semana

    Buenos Aires, Argentina IQVIA A tiempo completo

    Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Developing professional individual contributor who works...

  • Senior Site Activation Specialist

    hace 11 horas

    Buenos Aires, Buenos Aires C.F., Argentina Dev-Pro A tiempo completo

    Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.May also include maintenance activities.Developing professional individual contributor who works...

Senior Site Manager

hace 1 mes

Buenos Aires, Argentina Johnson & Johnson A tiempo completo

At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity.

Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.

When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.

At Janssen, we’re creating a future where disease is a thing of the past. We’re the Pharmaceutical Companies of Johnson & Johnson, working tirelessly to make that future a reality for patients everywhere by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart. We focus on areas of medicine where we can make the biggest difference: Cardiovascular & Metabolism, Immunology, Infectious Diseases & Vaccines, Neuroscience, Oncology, and Pulmonary Hypertension.
We are Janssen.
Our mission drives us.
Our patients inspire us.

We are searching the best talent for **Senior Site Manager **to be in **Buenos Aires, Argentina **(remote).

Purpose: The Senior Site Manager serves as the primary contact point between the Sponsor and the Investigational Site. The Sr. Site Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study startup through to site closure. Responsibilities may include assisting with site selection, pre-trial assessment, recruitment and retention planning, site initiation, on-site and remote monitoring and close-out activities. The Senior Site Manager will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and Clinical Trial Manager (CTM) to ensure overall site management while performing trial related activities for assigned protocols. The Sr. Site Manager may contribute to process improvement, training and mentoring of other Site Managers.

As the Senior Site Manager, you will:

- Act as primary local company contact for assigned sites for specific trials, may participate in site feasibility and/or pre-trial site assessment visits, and attend/participate in investigator meetings as needed.
- Execute activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management and site/study close-out according to SOPs, Work Instructions and policies. As well as implement analytical risk based monitoring model at the site level and work with the site to ensure timely resolution of issues found during monitoring visits.
- Ensure site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases. Responsible in close collaboration with LTM and central study team for the activities during site activation phase in order to speed up the process and activate the site in shortest possible timeframe.
- Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas.
- Ensure site study supplies are adequate for trial conduct.
- Ensure site staff complete data entry and resolve queries within expected timelines.
- Ensure accuracy, validity and completeness of data collected at trial sites
- Ensure that all Adverse Events (AE) /Serious Adverse Events (SAEs )/Product Quality Complaints (PQCs) are reported within the required reporting timelines and documented as appropriate.
- Maintains complete, accurate and timely data and essential documents in relevant systems utilized for trial management.
- Fully documents trial related activities, in particular monitoring. Writes visit reports and follow-up letter in accordance with the SOPs. Promptly communicates relevant status information and issues to appropriate stakeholders.
- Reviews study files for completeness and ensures archiving retention requirements are met, including storage in a secure area at all times.

**Qualifications**:

- A minimum of a bachelor’s degree is required, preferably in a health or science related field.
- A minimum of four (4) years of experience is required.
- Experience in clinical trials or working as a Site Manager (CRA) is preferred.
- Good knowledge of ICH-GCP, Standard Operating Procedures (SOP), local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines is preferred.
- Strong IT skills in appropriate software and systems is preferred.
- This position may require up to 25% of travel.
- Proficiency in speaking and writing in English (intermediate level) is required.

GIFTS