Clinical Trial Administrator Ii
3 semanas atrás
Company Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. Only CVs in English will be accepted. You will be responsible for Customization of Site ICF/patient documents before sending it to sites EC-IRB submissions Site Room, Veeva Vault, electronic Trial Master file and CTMs (including set up and maintenance) Site file preparation for SIV (Printing and assembling documents) Collection and filing documents from sites for MOH submissions Coordinate the translation of documents Collection/QC/filing of site documents All documents required per Data Management Plan, not limited to Investigational Product Release-Enabling Document Accesses to systems: Collecting vendor access information from sites in the format requested #LI-Hybrid Qualifications College/University degree or an equivalent combination of education, training & experience Minimum 1 year of industry experience Administrative work experience, preferably in an international setting Local regulations knowledge Prior experience in Clinical Research Full working proficiency in English and Portuguese Ability to plan and work in a dynamic team environment Communication and collaboration skills Additional Information Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company. #J-18808-Ljbffr
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Clinical Project Manager
3 semanas atrás
Sao Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro**Clinical Project Manager****(Level Depends on Experience)****Job Purpose/Summary**: Responsible for management and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client’s goals of time, budget and quality performance are met. The Clinical Project Manager I is expected to require support and guidance from Directors and/or...
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Clinical Project Manager **Level Dependent on Experience**
3 semanas atrás
São Paulo, Brasil CTI Clinical Trial and Consulting Services Tempo inteiroClinical Project Manager – Level Dependent on Experience CTI Clinical Trial and Consulting Services is a global, privately held, full‑service clinical contract research organization focused on advancing treatments for chronically and critically ill patients. We support clinical research throughout the life cycle of development, from drug concept to...
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Clinical trial specialist
2 semanas atrás
São Paulo, Brasil Anonymous Tempo inteiroJob Description:As a Clinical Research Associate (CRA), you will play a pivotal role in ensuring the integrity and compliance of clinical trials. You will be responsible for monitoring investigator sites, identifying potential issues, and implementing corrective actions to ensure trial success.Required Skills and Qualifications:
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Clinical Trial Administrator Ii
Há 2 dias
Sao Paulo, Brasil PSI CRO Tempo inteiro**Company Description** PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Join our international team and be the key support to...
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Clinical Trial Manager
3 semanas atrás
São Paulo, Brasil ICON Tempo inteiroClinical Trial Manager - Sao Paulo, Brazil (Homebased) ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Role: Clinical Trial Manager Location:...
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Clinical Trial Manager
2 semanas atrás
São Paulo, Brasil beBeeClinicalResearch Tempo inteiroJob Role: Clinical Research Associate - Site Management Job Description: This role involves site monitoring and management for clinical trials. The Clinical Research Associate (CRA) will be responsible for ensuring compliance with the protocol, regulatory requirements, and Good Clinical Practice (GCP). This includes conducting on-site visits to monitor...
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Clinical Trial Specialist
2 semanas atrás
São Paulo, Brasil beBeeClinicalResearchAssociate Tempo inteiroJob Description:As a Clinical Research Associate (CRA), you will play a pivotal role in ensuring the integrity and compliance of clinical trials. You will be responsible for monitoring investigator sites, identifying potential issues, and implementing corrective actions to ensure trial success.Required Skills and Qualifications:Strong analytical and...
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Clinical Trial Educator
Há 5 dias
Sao Paulo, Brasil Novasyte Tempo inteiroJob Overview The Clinical Trial Educator (CTE) will provide information and education on clinical trial inclusion and exclusion criteria to trial coordinators and healthcare providers. Also provides in-service presentations with the goal to increase patient enrollment. Works in partnership with CRAs and other field-based medical teams for optimal trial...
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Clinical Trial Specialist
2 semanas atrás
São Paulo, Brasil beBeeClinicalResearchAssociate Tempo inteiroJob Description: As a Clinical Research Associate (CRA), you will play a pivotal role in ensuring the integrity and compliance of clinical trials. You will be responsible for monitoring investigator sites, identifying potential issues, and implementing corrective actions to ensure trial success. Required Skills and Qualifications: Strong analytical and...
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Clinical Trial Specialist
2 semanas atrás
São Paulo, Brasil beBeeClinicalResearchAssociate Tempo inteiroJob Description: As a Clinical Research Associate (CRA), you will play a pivotal role in ensuring the integrity and compliance of clinical trials. You will be responsible for monitoring investigator sites, identifying potential issues, and implementing corrective actions to ensure trial success. Required Skills and Qualifications: Strong analytical and...