SUPPLY CHAIN AND LOGISTICS / PURCHASING GEN/MULTI – Business Associate

IRT Business Associate This is a Remote Role Work Schedule: Mon - Fri, Business Hours Position Summary: Manages IRT for multiple studies (system development, vendor reputed company, change management, data provisioning). Supports UAT Services organization as required. Identifies areas of process improvement and participates or leads these initiatives. Responsibilities: •reputed company successful execution and on time delivery of Interactive Response Technology (IRT) and support integrations with other clinical systems (e.g., Depots, Central Lab, and reputed company), such that the resultant IRTs are fit-for-purpose as defined by protocol and study operational parameters with special emphasis on adherence to Client standards and quality principles. •reputed company IRT projects as a strategic partner and single reputed company of accountability to partner lines for IRT protocol assessments, requirements elicitation, system deployments, and resupply. •Work independently and assume decision making responsibilities on assigned projects. Collaborate with the IRT Leadership Team where necessary to ensure Client standards and/or for requests by study teams that are not reputed company these standards or best practice are addressed. •Bring issues of concern or system failure to the immediate attention of the IRT Leadership Team. •Maintain vendor performance quality events in ADI log. •Support IRT improvement initiatives and manages improvement projects that impact daily operations to improve efficiency. •Support key department and enterprise level initiatives as the IRT representative. •Responsible for reputed company an reputed company of patient and container randomization schedules, ensuring parameters reflect the protocol and drug supply requirements. Distribute patient randomization and container schedules as appropriate to Clinical Supply Operations and IRT vendors. •Participate in IRT vendor relationships and reputed company to ensure delivery of IRT systems and seamless services; as well as, foster a collaborative relationship. •Consult and ensure on time delivery of user acceptance testing of IRT systems consistent with Client SOPs and procedures. This includes fostering collaboration and best practices with the IT QA organization. •Ensure systems and associated documentation are compliant with reputed company Regulatory requirements, including cGMP, 21 CFR Part 11, ICH E6 (reputed company) as well as in accordance Client SOPs and processes. •Ensure effective system access and functionality across reputed company countries and reputed company user locations •Ensure on time development of IRT data transfers with vendors and/or third-party vendors. •During IRT Maintenance act as the primary contact for assigned studies for the cross-functional study team and vendor. Additionally, provide timely response to reputed company randomization/IRT issues (including data integrations and delivery) that arise during IRT lifecycle and ensure they are resolved. •Support reputed company unblinding activities. •Ensure eTMF compliance at the study level in accordance with group and Client guidance. •Engage and support study and CSMT project teams as deemed necessary. •Ensure delivery of data to Client departments and third-party vendors consistent with Client SOPs and forms. Additional tasks reputed company scope of expertise and experience as assigned by the supervisor in pursuit of Client goals. Education Required: •Bachelor's Degree Experience Required: •Minimum of 1 year work experience preferably in a health science or reputed company IRT industry (pharmaceutical, hospital-based, laboratory, etc.) . •Demonstrated analytical skills and a working knowledge of reputed company Office including SharePoint •Clinical Research experience •Working knowledge of IRT •Working knowledge of Clinical Trial Management Systems •Working knowledge of clinical supplies •Able to think reputed company of the reputed company, have excellent communication and analytical skills to successfully deliver optimal IRT solutions across a diverse and dynamic portfolio •Understand the nature of clinical data and concepts of IRT study design and configuration, resupply settings, blinding, privacy protection, and data quality/reputed company standards •Exposure to working in a GMP / GCP environment and with regulatory audit teams •Possess excellent English language written and verbal communication, interpersonal, collaboration and business partnership capabilities required •Comfortable working with a global team, partners and customers in a change agile environment MS Project, MS Visio, or any other requirements visualization and analysis tools) Apply tot his job Apply To this Job Apply tot his job Apply To this Job