13 publicaciones de empleo destacadas de event planning en buenos aires buenos aires (¡Están contratando!)

CRA II / Sr CRA
Fortrea —Buenos Aires, Buenos Aires
- Tiempo completo
Director - Cyber Security
Latino Legends —Buenos Aires, Buenos Aires
Postulación rápida
Senior AI Fullstack Developer
Marvik —Buenos Aires, Buenos Aires
GRC Engineer
FeverUp —Capital Federal, Buenos Aires
Postulación rápida
Backend Go Lead Engineer
ITC WORLDWIDE —Buenos Aires, Buenos Aires
- Por contrato
Postulación rápida
Senior Software Engineer, Fullstack
Webflow —Buenos Aires, Buenos Aires
Senior Scala Software Engineer
N-iX —Capital Federal, Buenos Aires
Postulación rápida
Senior PHP Backend Engineer
FeverUp —Buenos Aires, Buenos Aires
Postulación rápida
Senior Database Reliability Engineer
Sezzle —Capital Federal, Buenos Aires
Tech Lead
FeverUp —Buenos Aires, Buenos Aires
Postulación rápida
Junior Commercial Projects Coordinator
CIAL D&B Services Inc —Capital Federal, Buenos Aires
- Tiempo completo
Postulación rápida
Administrative Business Partner, LCS and Partners Activation
Google —Buenos Aires, Buenos Aires
- Tiempo completo
3h
Strategic Partner Manager, Scaled Partnerships
Google —Buenos Aires, Buenos Aires
- Tiempo completo
9h

More jobs to discover

Find similar jobs that you might be interested in.

Director - Cyber Security
Latino Legends —Buenos Aires, Buenos Aires
Compensation: USD $85,000–$120,000 per year + performance bonus. Paid Time Off: 15 days annually. We're seeking an experienced Director, Consulting to provide…
Postulación rápida

Quiero recibir la alerta de empleo más reciente para event planning en buenos aires buenos aires

Al ingresar a tu cuenta, aceptas las Condiciones del servicio de SimplyHired y das tu consentimiento a nuestra Política de privacidad y Cookies.

Explorar empleos en más ubicaciones

event planning jobs near buenos aires buenos aires

Empleos de Full Stack Developer en Buenos Aires, Buenos Aires

Empleos de Backend Developer en Buenos Aires, Buenos Aires

Empleos de Business Analyst en Buenos Aires, Buenos Aires

Empleos de Business Intelligence en Provincia De Buenos Aires

Empleos de Business Intelligence en Parque Chas, Buenos Aires

Empleos de Entry Level Developer en Work From Home

Empleos de C++ Developer en Buenos Aires, Buenos Aires

Empleos de Software Developer, Junior en Rosario, Santa Fe

Empleos de Back End Developer en Remoto+argentina

Empleos de Junior Fullstack Developer en Buenos Aires, Buenos Aires

Empleos de Back End Developer en Florida, Buenos Aires

Empleos de Full Stack Developer en Desde Casa

Empleos de Full Stack Developer en Resistencia, Chaco

Empleos de Full Stack Developer en Capital Federal, Buenos Aires

Empleos de Strategic Finance en Remoto

Empleos de Finance Partner en Buenos Aires, Buenos Aires

Empleos de Hr Business Partner en Martínez, Buenos Aires

Empleos de Abogado Junior en Buenos Aires, Buenos Aires

Empleos de Data Engineer en Buenos Aires, Buenos Aires

Empleos de Engineer Electronic en Buenos Aires, Buenos Aires

CRA II / Sr CRA

Fortrea -
Buenos Aires, Buenos Aires

Postulate ahora

Detalles del empleo

Tiempo completo

Descripción completa del empleo

Summary of Responsibilities:

Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.
Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.
Prepares and implements project plans related to Clinical Monitoring responsibilities.
Ensures the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements.
Safeguards data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines on Fortrea or client data management systems.
Confirms Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial.
Guarantees that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements.
Ensures adherence to global quality control and CRA performance metrics.
Ensures audit readiness at site level.
Acts in the project role of a Lead CRA as assigned.
General On-Site Monitoring Responsibilities:
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study. Ensure the protection of study subjects or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
Ensure the integrity of the source data reported by careful source document review. Monitor data for missing or implausible data.
Ensure study data completeness, accuracy, consistency, and compliance; identify deficiencies, deviations and discrepancies, and initiate corrective action as required.
Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy.
Travel, including air travel, may be required and is an essential function of the job.
Prepare and submit accurate and timely trip reports.
Independently perform eCRF review, 100% source data verification, query generation and resolution against established data review guideline with or without direct supervision, on Fortrea or client data management systems, as assigned by management.
Assist with the administration of clinical research projects, recruiting investigators (if applicable), collecting investigator documentation and site management.
Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/eClinical systems.
Track IP shipments and supplies, as needed.
Track and follow-up on serious adverse events as assigned.
Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met.
Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned.
Attend investigators’ meetings (if applicable), project team meetings and teleconferences, and others as needed.
Present training content for site initiation.
Assist with training of new employees (e.g., co-monitoring).
All other duties as needed or assigned.

Qualifications (Minimum Required):

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.
Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.
Thorough knowledge of monitoring procedures.
Basic understanding of the clinical trial process.
Fluent in local office language and in English, both written and verbal.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience (Minimum Required):

External Candidates:
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). AND
A minimum of 2 years of Clinical Monitoring experience.
Internal Candidates:
Internal candidates with a minimum of 2 years of Clinical Monitoring experience.
Ability to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines.
Ability to work with minimal supervision.
Have an understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
Good planning, organization, and problem-solving abilities.
Works efficiently and effectively in a matrix environment.

Preferred Qualifications Include:

Thorough working knowledge of Fortrea SOPs for site monitoring.
One (1) or more additional years of experience in a related field (i.e., medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred.
Phase I monitoring experience.
Life Science or Nursing qualification.
Specific skills, systems, certifications, and/or licenses preferred.
Personal characteristics (leadership, problem solving, interpersonal skills).
Good attention to detail.
Methodical approach to work.
Good understanding of medical and clinical research terminology and clinical research processes.
An understanding of the basics of physiology, pharmacology, and medical devices (when applicable).
Good understanding of the principles of ICH GCP, ISO 14155 (if applicable) and local regulatory requirements.
Good computer literacy with working knowledge of PCs, Windows and Microsoft Office applications.
Good oral and written internal and external communication. Strong interpersonal team and organizational skills, personal presentation. The ability to communicate effectively in English.
Focus on Customer.
Innovate and Change.
Pursue Scientific and Process Excellence.
Work with Others.
Achieve Results.
Ability to maintain confidentiality of data and information during interactions with staff at all levels and across studies and sponsors.
Demonstrated ability to conduct clinical operations activities most effectively and efficiently.
Good analytical and negotiation skills.
Experience using e-clinical systems [e.g., clinical trial management system (CTMS)].
For medical device positions, experience in providing customer service to device end users.

Physical Demands/Work Environment:

Must be able to sit at a computer for long periods of time.
Must be able to use hands to finger, handle or touch objects, tools or controls, including a computer keyboard, for up to 8 hours per day.
Standard office and/or home working environment.
Clinical Research Unit and hospital environment (administrative only).
Risk of eye strain.
Will involve outside of normal office hours as required by the role.
Travel Requirement is 60% of the time (traveling to study sites).

Learn more about our EEO & Accommodations request here .

Postulate ahora

Refiná tu búsqueda

event planning empleos en buenos aires buenos aires

CRA II / Sr CRA

Director - Cyber Security

Senior AI Fullstack Developer

GRC Engineer

Backend Go Lead Engineer

Senior Software Engineer, Fullstack

Senior Scala Software Engineer

Senior PHP Backend Engineer

Senior Database Reliability Engineer

Tech Lead

Junior Commercial Projects Coordinator

Administrative Business Partner, LCS and Partners Activation

Strategic Partner Manager, Scaled Partnerships

More jobs to discover

Quiero recibir la alerta de empleo más reciente para event planning en buenos aires buenos aires

Related Searches

Explorar empleos en más ubicaciones

Herramientas para candidatos

Herramientas para empresas

Explorar

Mantente conectado