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CLINICAL RESEARCH ASSOCIATE II – CRA II OR CRA IIIArgentina - RemoteWho We Are
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. Nothing stops us in the search for knowledge. 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. Diversity of color, belief, sexual orientation, religion, or any other characteristic are very welcome in all open positions at our company. It is a fundamental part of Intrials to constantly think and implement actions that reinforce the importance of good coexistence with all the people who are part of our DNA and together, to leverage and build true impactful results in our society.
Primary responsibilities include, but are not limited to:
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);▪ Participate in meetings / teleconferences with Sponsor and PM;▪ Act as main point of contact for study sites;▪ Provide support to PM and more experienced CRAs in the study coordination activities, as applicable;▪ Perform coaching activities for less experienced CRAs.
Requirements:
▪ 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; OR▪ 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;▪ Excellent organizational abilities and interpersonal relationships; oriented to solve problems; self-confidence;▪ Available to travel intensively and ability to manage travel schedules;▪ Knowledge of ICH-GCP, local and international guidelines;▪ Computer skills on Windows environment and Microsoft Office tools;▪ Advanced knowledge of English; to undesrtand, write and speak.▪ Experience in rheumatology is desirable, but not mandatory