CRA II - Sponsor dedicated - Brazil Home BasedSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.Job responsibilities• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans.• Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/patient. Assesses factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.• Per the Clinical Monitoring/Site Management Plan (CMP/SMP): o Assesses site processeso Conducts Source Document Review of appropriate site source documents and medical recordso Verifies required clinical data entered in the case report form (CRF) is accurate and completeo Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelineso Utilizes available hardware and software to support the effective conduct of the clinical study data review and captureo Verifies site compliance with electronic data capture requirements• May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol.• Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations.• Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.• For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met.• May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements.• Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements.• Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.• Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes; completes assigned training as required.• For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Additional responsibilities include:o Site support throughout the study lifecycle from site identification through close-outo Knowledge of local requirements for real world late phase study designso Chart abstraction activities and data collectiono Collaboration with Sponsor affiliates, medical science liaisons and local country staffo The SMA II may be requested to train junior staffo Identify and communicate out of scope activities to Lead CRA/Project Managero Proactively suggest potential sites based on local knowledge of treatment patterns, patient advocacy and Health Care Provider (HCP) associationsQualifications• Bachelor's degree or RN in a related field or equivalent combination of education, training and experience• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements• Must demonstrate good computer skills and be able to embrace new technologies• Excellent communication, presentation and interpersonal skills• Ability to manage required travel of up to 75% on a regular basisAt Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. If your past experience doesn't align perfectly, we encourage you to apply anyway. At times, we take into consideration transferable skills from previous roles.
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