Clinical Research Associate 2
Há 5 dias
Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned. General On-Site Monitoring Responsibilities. Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. Ensure audit readiness at the site level. Track and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs. 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. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Basic knowledge of Regulatory Guidelines. Basic understanding of the clinical trial process. Fluent in local office language and in English, both written and verbal. Experience (Minimum Required): 1 year of experience as a CRA, operating with Portuguese centers and regulation. Basic understanding of Regulatory Guidelines. Valid Driver's License. Preferred Qualifications Include: One (1) or more year's additional experience in a related field (i.e., medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred Experience using a clinical trial management system (CTMS). Learn more about our EEO & Accommodations request here.
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Clinical Research Associate 2
2 semanas atrás
Oeiras, Portugal IQVIA Tempo inteiroClinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.E., Good Clinical Practice and International Conference on...
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Clinical Research Associate 2
Há 7 dias
Oeiras, Portugal Fortrea Tempo inteiroClinical Research Associate 2 - FSO Model - Portugal Join to apply for the Clinical Research Associate 2 - FSO Model - Portugal role at Fortrea. Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Ensures the implementation of...
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Clinical Research Associate 2
1 semana atrás
Oeiras, Lisboa, Portugal IQVIA Tempo inteiroClinical Research AssociateYour Responsibilities Will IncludePerforming site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization...
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Experienced Clinical Research Associate
Há 5 dias
Oeiras, Portugal IQVIA Tempo inteiroClinical Research Associate needed in Porto to perform site visits and support recruitment plans.
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Experienced Clinical Research Associate
2 semanas atrás
Oeiras, Portugal IQVIA Tempo inteiroA leading global provider of clinical research services is looking for a Clinical Research Associate based in Porto. This entry-level, full-time role requires performing site selection, initiation, monitoring, and close-out visits while supporting the development of subject recruitment plans. Applicants should hold a relevant university degree and possess...
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Experienced Clinical Research Associate
Há 5 dias
Oeiras, Portugal IQVIA Tempo inteiroSenior Clinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.E., Good Clinical Practice and International Conference on...
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Senior Clinical Research Associate
1 semana atrás
Oeiras, Portugal MSD Tempo inteiroJob Description We are one of the leading pharmaceutical companies in the world, dedicated to the discovery, development, and delivery of innovative medicines that improve health and quality of life for people. With a strong global presence and an unwavering commitment to scientific research, our mission is to transform health through innovation and...
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Senior Clinical Research Associate
1 semana atrás
Oeiras, Portugal MSD Portugal Tempo inteiroJob DescriptionWe are one of the leading pharmaceutical companies in the world, dedicated to the discovery, development, and delivery of innovative medicines that improve health and quality of life for people. With a strong global presence and an unwavering commitment to scientific research, our mission is to transform health through innovation and...
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Clinical Research Associate 2
1 semana atrás
Oeiras, Lisboa, Portugal Fortrea Tempo inteiroJob Overview:Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and closeout...
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Clinical Research Assoicate
Há 3 dias
Oeiras, Portugal IQVIA Tempo inteiroJob Description We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte . Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local...
