Experience Work with business to move custom sites to out-of-the-box sites in SharePoint. Develop solutions to satisfy requirements for the business Collaborate with senior SharePoint Migration consultants on what to do pre-migration and review sites post migration Develop SharePoint sites Provide training as needed Qualifications Migration experience is very helpful at least 2 years...

Job Description for Global Quality Solutions Representative  Responsibilities include but are not limited to: Partner with and support assigned functional groups, departments and regions to achieve the goals and objectives of the Global Quality Team Interact with the various business groups within the Global Quality team and supports their technology needs by partnering with IT to implement...

Job Description The Drug Development Project Manager acts as a central contact for information on a particular program and manages activities to develop programs. Ensures that concurrence between the team and management is achieved for program objectives and meets these objectives to achieve goals. Works with management staff and teams to create the development strategy, establish objectives,...

Role Description – Sr. Associate Compliance Auditing and Monitoring This position will assist E&C's Healthcare Law Auditing and Monitoring function supporting the Chief Compliance Officer in executing an effective compliance program. The Senior Compliance Auditor will assist the Manager, Healthcare Law Auditing & Monitoring and others to execute the annual plan by conducting audits and other...

· Leads preparation, review, and update of content for the development and maintenance of Core, US, EU and Canadian labeling and packaging components · Demonstrate a high-level understanding of labeling content requirements, regulations and guidance to guide labeling teams and support labeling strategies · Develop and maintain Target Product Profile, Company Core Data Sheet (CCDS) and local...

We are currently searching for a skilled Medical Affairs professional to join our client as a Senior Manager, Global Medical Affairs, Nephrology. The Senior Manager will be responsible for overseeing and assisting with nephrology projects, in alignment with the Global Medical Affairs Department goals and initiatives. Project work will span from early to late-stage and commercialized programs. Job...

Pharmica seeks a Case Processing Associate to support our client in the Princeton, NJ area. This is a position requiring a 40 hour/week and potential on-site presence, after their facilities reopen. This position is responsible for processing incoming AE information, including:   Case review, QC of safety data in ARGUS, data cleaning for previous cases in ARGUS, performing literature search...

Roles and Responsibilities Develop and execute against project plans for multiple, concurrent initiatives Partner with key stakeholders to manage priority projects and ensure tasks are delivered on time and with quality Keep the team organized and on track leveraging project management tools and methodologies - action item trackers, MS Teams sites, project status decks/reports, Gantt...

The CSV Auditor will provide expert advice and hands on capabilities to various types of audits that includes, but are not limited to, supplier audits, computerized systems audits, process audits and data integrity audits in the regulated pharmaceutical and medical device industry. Significant travel in excess of 50% is expected 1.Contribute to and perform all CSV audit activities including...

The GPV Auditor will lead and perform audits with a focus on Pharmacovigilance activities. Additional tasks are required to support the continuous improvement of the companies Quality System, inspection management, regulatory intelligence activities, SOP and WP management, validation activities, and project liaison activities.Significant travel in excess of 50% is expected 1. Pharmacovigilance Au...