The Senior Clinical Research Associate I (SCRA I)will perform monitoring and site management activities for Phase I-IV clinicalresearch projects to assess the progress of clinical projects at assignedinvestigative / physician sites (either on site or remotely) and to ensureclinical projects are conducted, recorded, and reported in accordance with theprotocol, Company and Sponsor standard operating procedures (SOPs), ICH-
GCP,and / or all applicable local and federal regulatory requirements.Performs all tasks routinely andindependently.May assume clinicalfunctional leadership tasks as assigned, acting as Lead CRA for a project orassessor of peers for sign-
off visit purposes (as approved).
GCP and / orGood Pharmacoepidemiology Practice (GPP) and protocol compliance.Uses judgment and experience to evaluateoverall performance of site and site staff and to provide recommendationsregarding site-
specific actions; immediately communicates / escalates seriousissues to the project team and develops action plans.Maintains a working knowledge of ICH / GCPGuidelines or other applicable guidance, relevant regulations, and companySOPs / processes.
Demonstrates diligence inprotecting the confidentiality of each subject / patient. Assesses factors thatmight affect subject / patient’s safety and clinical data integrity at aninvestigator / physician site such as protocol deviation / violations andpharmacovigilance issues.
oAssesses site processes
oConducts Source Document Review of appropriate site source documents andmedical records
oVerifies required clinical data entered in the case report form (CRF) isaccurate and complete via review of site source documents and medical records
oApplies query resolution techniques remotely and on site, and providesguidance to site staff as necessary, driving query resolution to closure withinagreed timelines
oUtilizes available hardware and software to support the effectiveconduct of the clinical study data review and capture
oVerifies site compliance with electronic data capture requirements
Verifies issues or risks associated with blinded orrandomized information related to IP. Applies knowledge of GCP / localregulations and organizational procedures to ensure IP is appropriately(re)labelled, imported and released / returned.
Ensures the investigator / physiciansite is aware of the requirement of archiving essential documents in accordancewith local guidelines and regulations.
Supports subject / patient recruitment, retention and awarenessstrategies.Enters data into trackingsystems as required to track all observations, ongoing status and assigned actionitems to resolution.
Must be able to quickly adapt to changing priorities to achieve goals / targets.
specific site team members are trained and compliantwith applicable requirements.
oSitesupport throughout the study lifecycle from site identification through closeout
oKnowledgeof local requirements for real world late phase study designs
oChartabstraction activities and data collection
oAsrequired, collaborate and build relationships with Sponsor and otheraffiliates, medical science liaisons and local country staff
oThe SMAII may be requested to train junior staff
oIdentifyand communicate out of scope activities to Lead CRA / Project Manager
oProactivelysuggest potential sites based on local knowledge of treatment patterns, patientadvocacy and Health Care Provider (HCP) associations
oIdentifyoperational efficiencies and process improvements
oDevelopcountry level informed consent forms
oCollaboratewith RWLP Regulatory team to ensure updated regulatory information is appliedand shared
oParticipatein bid defense meetings
Tasks, duties, and responsibilities as listed in this jobdescription are not exhaustive. The Company, at its sole discretion and with noprior notice, may assign other tasks, duties, and job responsibilities.
Equivalent experience, skills, and / or education will also be considered soqualifications of incumbents may differ from those listed in the JobDescription.
The Company, at its sole discretion, will determine whatconstitutes as equivalent to the qualifications described above.
Further,nothing contained herein should be construed to create an employment contract.Occasionally, required skills / experiences for jobs are expressed in briefterms.
Any language contained herein is intended to fully comply with allobligations imposed by the legislation of each country in which it operates,including the implementation of the EU Equality Directive, in relation to therecruitment and employment of its employees.