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Vagas de emprego na área de Marketing

São Paulo/SP cancel Pesquisador cancel
Localização:
São Paulo / SP
Salário:
a combinar

Código da vaga: V02509876

Publicada há:

Atribuições

Ind. Farmacêutica cargo: Monitor de pesquisa região: Sp vaga: Monitor de pesquisa clinica -cra local: São paulo - sp requisitos: Empresa parceira busca monitor de pesquisa clinica -cra para são paulo - sp descrição da vaga e responsabilidades: Purpose perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, clinical research associates may be accountable for development of project subject recruitment plan on a per site basis. Support work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Responsibilities · perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. · if applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. · provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. · administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. · evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (crf) completion and submission, and data query generation and resolution. May support start-up phase. · create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required st

Tipo de Vínculo

Efetivo

Localização:
São Paulo / SP
Salário:
a combinar

Código da vaga: V02508861

Publicada há:

Atribuições

Ind. Farmacêutica cargo: Monitor de pesquisa região: Sp vaga: Monitor de pesquisa clinica -cra local: São paulo - sp requisitos: Empresa parceira busca monitor de pesquisa clinica -cra para são paulo - sp descrição da vaga e responsabilidades: Purpose perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, clinical research associates may be accountable for development of project subject recruitment plan on a per site basis. Support work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Responsibilities · perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. · if applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. · provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. · administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. · evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (crf) completion and submission, and data query generation and resolution. May support start-up phase. · create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required st

Tipo de Vínculo

Efetivo

Localização:
São Paulo / SP
Salário:
a combinar

Código da vaga: V02508031

Publicada há:

Atribuições

Ind. Farmacêutica cargo: Monitor de pesquisa região: Sp vaga: Monitor de pesquisa clinica -cra local: São paulo - sp requisitos: Empresa parceira busca monitor de pesquisa clinica -cra para são paulo - sp descrição da vaga e responsabilidades: Purpose perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, clinical research associates may be accountable for development of project subject recruitment plan on a per site basis. Support work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Responsibilities · perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. · if applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. · provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. · administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. · evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (crf) completion and submission, and data query generation and resolution. May support start-up phase. · create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required st

Tipo de Vínculo

Efetivo

Localização:
São Paulo / SP
Salário:
a combinar

Código da vaga: V02506039

Publicada há:

Atribuições

Ind. Farmacêutica cargo: Monitor de pesquisa região: Sp vaga: Monitor de pesquisa clinica -cra local: São paulo - sp requisitos: Empresa parceira busca monitor de pesquisa clinica -cra para são paulo - sp descrição da vaga e responsabilidades: Purpose perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, clinical research associates may be accountable for development of project subject recruitment plan on a per site basis. Support work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Responsibilities · perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. · if applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. · provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. · administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. · evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (crf) completion and submission, and data query generation and resolution. May support start-up phase. · create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required st

Tipo de Vínculo

Efetivo

Localização:
São Paulo / SP
Salário:
a combinar

Código da vaga: V02505284

Publicada há:

Atribuições

Ind. Farmacêutica cargo: Monitor de pesquisa região: Sp vaga: Monitor de pesquisa clinica -cra local: São paulo - sp requisitos: Empresa parceira busca monitor de pesquisa clinica -cra para são paulo - sp descrição da vaga e responsabilidades: Purpose perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, clinical research associates may be accountable for development of project subject recruitment plan on a per site basis. Support work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Responsibilities · perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. · if applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. · provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. · administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. · evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (crf) completion and submission, and data query generation and resolution. May support start-up phase. · create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required st

Tipo de Vínculo

Efetivo

Localização:
São Paulo / SP
Salário:
a combinar

Código da vaga: V02504630

Publicada há:

Atribuições

Ind. Farmacêutica cargo: Monitor de pesquisa região: Sp vaga: Monitor de pesquisa clinica -cra local: São paulo - sp requisitos: Empresa parceira busca monitor de pesquisa clinica -cra para são paulo - sp descrição da vaga e responsabilidades: Purpose perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, clinical research associates may be accountable for development of project subject recruitment plan on a per site basis. Support work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Responsibilities · perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. · if applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. · provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. · administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. · evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (crf) completion and submission, and data query generation and resolution. May support start-up phase. · create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required st

Tipo de Vínculo

Efetivo

Localização:
São Paulo / SP
Salário:
a combinar

Código da vaga: V02503552

Publicada há:

Atribuições

Ind. Farmacêutica cargo: Monitor de pesquisa região: Sp vaga: Monitor de pesquisa clinica -cra local: São paulo - sp requisitos: Empresa parceira busca monitor de pesquisa clinica -cra para são paulo - sp descrição da vaga e responsabilidades: Purpose perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, clinical research associates may be accountable for development of project subject recruitment plan on a per site basis. Support work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Responsibilities · perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. · if applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. · provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. · administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. · evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (crf) completion and submission, and data query generation and resolution. May support start-up phase. · create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required st

Tipo de Vínculo

Efetivo

Localização:
São Paulo / SP
Salário:
a combinar

Código da vaga: V02502310

Publicada há:

Atribuições

Ind. Farmacêutica cargo: Monitor de pesquisa região: Sp vaga: Monitor de pesquisa clinica -cra local: São paulo - sp requisitos: Empresa parceira busca monitor de pesquisa clinica -cra para são paulo - sp descrição da vaga e responsabilidades: Purpose perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, clinical research associates may be accountable for development of project subject recruitment plan on a per site basis. Support work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Responsibilities · perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. · if applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. · provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. · administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. · evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (crf) completion and submission, and data query generation and resolution. May support start-up phase. · create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required st

Tipo de Vínculo

Efetivo

Localização:
São Paulo / SP
Salário:
a combinar

Código da vaga: V02501599

Publicada há:

Atribuições

Ind. Farmacêutica cargo: Monitor de pesquisa região: Sp vaga: Monitor de pesquisa clinica -cra local: São paulo - sp requisitos: Empresa parceira busca monitor de pesquisa clinica -cra para são paulo - sp descrição da vaga e responsabilidades: Purpose perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, clinical research associates may be accountable for development of project subject recruitment plan on a per site basis. Support work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Responsibilities · perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. · if applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. · provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. · administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. · evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (crf) completion and submission, and data query generation and resolution. May support start-up phase. · create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required st

Tipo de Vínculo

Efetivo

Localização:
São Paulo / SP
Salário:
a combinar

Código da vaga: V02501032

Publicada há:

Atribuições

Ind. Farmacêutica cargo: Monitor de pesquisa região: Sp vaga: Monitor de pesquisa clinica -cra local: São paulo - sp requisitos: Empresa parceira busca monitor de pesquisa clinica -cra para são paulo - sp descrição da vaga e responsabilidades: Purpose perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, clinical research associates may be accountable for development of project subject recruitment plan on a per site basis. Support work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Responsibilities · perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. · if applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. · provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. · administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. · evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (crf) completion and submission, and data query generation and resolution. May support start-up phase. · create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required st

Tipo de Vínculo

Efetivo