.For more than 75 years, Grifols has worked to improve the health and well-being of people around the world. We are a global healthcare company that produces essential plasma-derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services they need to deliver expert medical care.Headquartered in Barcelona, Spain, Grifols has over 20.000 employees in 30 countries. Grifols' three main divisions - Bioscience, Diagnostic and Hospital - develop, manufacture and market innovative products and services available in more than 100 countries.With the world's largest network of plasma donation centers, Grifols, through its Bioscience Division, is a leading producer of essential plasma-derived medicines for the treatment of rare, chronic, and sometimes life-threatening conditions. To help ensure a reliable and consistent source of plasmaderived medicines worldwide, we have an integrated production process that begins with plasma collection and continues through fractionation and purification at our three facilities located in Spain (Barcelona) and the United States (Clayton, North Carolina, and Los Angeles, California). Key products include immunoglobulins, alpha-1 antitrypsin, albumin, clotting factors and specialty products.Help us lead one of the world's largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people.From the Clinical Development department we are looking for a Clinical Research Associate.YOUR TASK AND RESPONSABILITIESAs a Clinical Research Associate you will provide support in the oversight and management of vendors. You will conduct clinical monitoring to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols and you will assist in the clinical trial management to ensure timelines and metrics are met and maintained throughout the study.You will able to:Review and track comments of monitoring reports generated by CRO as part of Sponsor Oversight of Vendor Clinical Site Monitoring activities in conformance to the clinical trial protocol, company SOPs, GCP/ICH Guidelines and all applicable regulatory requirements.Perform Sponsor Site Visits as part of Sponsor Oversight of Vendor Clinical Site Monitoring activities in conformance to the clinical trial protocol, company SOPs, GCP/ICH Guidelines and all applicable regulatory requirements.Assist in the management of vendor performance during conduct of the study.Assist with expedited identification, retrieval, and review of study documents particularly those required for site activation/study start-up
