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Clinical Research Associate Associ De Recherche Clinique
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- Clinical Research Associate 35Pharma is a clinical-stage biopharmaceutical company that designs and develops innovative therapeutics for life threatening lung diseases, and musculoskeletal and metabolic disorders.
- Role:The Clinical Research Associate will be responsible for clinical monitoring activities at clinical sites to ensure compliance with the clinical protocol and study procedures, as well as all applicable regulations, guidelines, quality industry standards, internal standard operating procedures (SOPs) and policies.
- The Clinical Research Associate will be responsible to conduct on-site and remote monitoring visits, to review and collect sites essential documents required for the trial master file (TMF), and be the primary point of contact with sites for the protocol, recruitment status, and essential documents collection.
- Minimum of 2 years’ experience in a pharmaceutical or biotechnology company or CRO, in a clinical research associate role conducting on-site monitoring visits.
- Proficiency in required softwares (Word, Excel, Power Point), clinical trial systems (i.e., EDC, eTMF, IRT, eCOA) and computer skills.
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