Clinical Research Associate

Overview Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies and clinical investigations: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. Key Responsibilities Identify investigator sites and participate in the feasibility process for new studies Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, e.g. ICH GCP Perform visits remotely according to foreseen applicable procedures and timeframes Interact with the Trial Start-up team and support collecting the documents or information necessary for the ethical and administrative submission Work closely with the sites to ensure that the planned recruitment targets are in line with the study plan/projections and motivate Investigators to achieve the targets Check the correct submission and completion of informed consent forms Manage the progress of assigned studies by tracking regulatory submissions and approvals, case report form (CRF) completion and submission, and data query generation and resolution Verify that serious adverse events have been reported using a SAE form, according to OPIS and/or Sponsor procedures Maintain all files and documentation pertaining to the studies and ensure that site documents are available for filing into TMF and correct archiving of files on study completion Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation Requirements Therapy Area Experience: Dermatology, Cardiology, Gastrointestinal Disorders Location: Dallas or Houston and/or surroundings University degree in a scientific/life science field At least 3 years of experience in managing and conducting clinical trials In depth knowledge of ICH GCP principles Able to carry out independently all the activities related to the monitoring of clinical trials Good knowledge of Office Suite (Word, Excel, PowerPoint) Organizational and problem-solving skills Excellent written and verbal communication skills including good command of English language No restrictions to travel onsite What we offer We offer a competitive salary with other benefits/bonuses and opportunity to develop your professional career with an expanding and growing company. Additional information Please read the information notice on the processing of personal data in the candidates information section of our company website. Who we are Founded in 1998 in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects. OPIS added value lies in its highly specialized professionals who can assist their clients using their deep know-how and experience to guarantee a top-quality level of Clinical Trial Management and ability to operate in a wide range of fields (medical writing, scientific and statistical consultancy for trial design, regulatory activities, pharmacovigilance, etc.) always contributing to our clients’ challenging achievements. This page is hosted by JazzHR and uses cookies for technical and analytical purposes. For details regarding the processing of your application data by OPIS, please refer to our: Pivacy Policy Candidate Privacy Policy #J-18808-Ljbffr