Global Clinical Trial Assistant
Hace 4 días
, México
Intrials Clinical Research
Jornada completa
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CLINICAL RESEARCH ASSOCIATE II – CRA II OR CRA III 1-year fixed-term position / Mexico
- Remote Intrials is a disruptive company with all the attributes that a CRO must master. We mix innovative projects with the necessary skills to provide a full service. Transforming people's lives through science when it comes to solving the challenges of our clients' projects in a focused and exclusive fashion. Diversity & Inclusion are essential to continue building our history of innovation. Ensure that the clinical study is conducted according to the ICH-GCP guidelines, the local and international regulations as well as according to Intrials or Sponsor’s SOPs; ▪ Ensure that clinical study data are accurate and verifiable; ▪ Identify and perform the corresponding quality controls on source documents; ▪ Perform monitoring activities and visits (on-site and/or remote): Site Selection Visit (SSV), Site Initiation Visits (SIV), Interim Monitoring Visit (IMV) and Close-out Visit (COV); ▪ Degree in Health Sciences or equivalent (Pharmacy, Biology, Biomedicine, Nursing, other); ▪ Reliable academic background and at least 2 years of experience in clinical research as a CRA at CRO, ARO or pharmaceutical company for CRA II; Reliable academic background and at least 4 years of experience in clinical research as a CRA at CRO, ARO or pharmaceutical company for CRA III; ▪ Knowledge of ICH-GCP, local and international guidelines; ▪ Computer skills on Windows environment and Microsoft Office tools; ▪ Advanced knowledge of English; Experience in rheumatology is desirable, but not mandatory
- Remote Intrials is a disruptive company with all the attributes that a CRO must master. We mix innovative projects with the necessary skills to provide a full service. Transforming people's lives through science when it comes to solving the challenges of our clients' projects in a focused and exclusive fashion. Diversity & Inclusion are essential to continue building our history of innovation. Ensure that the clinical study is conducted according to the ICH-GCP guidelines, the local and international regulations as well as according to Intrials or Sponsor’s SOPs; ▪ Ensure that clinical study data are accurate and verifiable; ▪ Identify and perform the corresponding quality controls on source documents; ▪ Perform monitoring activities and visits (on-site and/or remote): Site Selection Visit (SSV), Site Initiation Visits (SIV), Interim Monitoring Visit (IMV) and Close-out Visit (COV); ▪ Degree in Health Sciences or equivalent (Pharmacy, Biology, Biomedicine, Nursing, other); ▪ Reliable academic background and at least 2 years of experience in clinical research as a CRA at CRO, ARO or pharmaceutical company for CRA II; Reliable academic background and at least 4 years of experience in clinical research as a CRA at CRO, ARO or pharmaceutical company for CRA III; ▪ Knowledge of ICH-GCP, local and international guidelines; ▪ Computer skills on Windows environment and Microsoft Office tools; ▪ Advanced knowledge of English; Experience in rheumatology is desirable, but not mandatory