Barbara Wells Email & Phone Number

Remote

Remote

• Manage key, top-10 pharmaceutical company accounts at the senior business level
• Build trusted advisory relationships with key clients, ensuring overall satisfaction with our technology solutions
• Publications Subject Matter Expert: advise internal resources on publications best practices and terminology. Recommend configurations and workflows to clients that ensure adherence to industry standards
• Prioritize and drive resolution on escalated client issues
• Prepare and present custom training presentations and guides based on client needs and audiences
• Supervise and mentor Client Engagement Specialists

Research Triangle Park, NC

• Developed communications and publications plans for infectious disease treatments
• Planned, chaired and facilitated external expert scientific advisory boards
• Established and maintained professional relationships with key scientific and medical leaders in the infectious disease field
• Selected and managed vendors to deliver communications activities and logistical support for advisory boards and external meetings
• Developed a GSK Scientific Publishing intranet site using SharePoint to inform and train GSK personnel on publication policies and practices
• Expanded and managed the use of GSK’s offshore staff to conduct publication reviews and approvals via Datavision.

Research Triangle Park, NC

Contractor to GlaxoWellcome, see GlaxoSmithKline entry above for duties and accomplishments.

• Managed protocol development of Phase I – III HIV / AIDS pediatric and women’s health studies in the NIH-sponsored AIDS Clinical Trials Group (ACTG)
• Produced several fast track protocols in response to scientific breakthroughs and industry initiatives which led to publication in major scientific journals
• Coordinated meetings and symposia, working with outside speakers, scientists and HIV community representatives.
• Supervised a Clinical Trials Specialist and a Study Coordinator

• Wrote and edited patient consent forms and regulatory memoranda
• Collected clinical data, created treatment schedules, and prepared all submissions of protocols and other materials to the Institutional Review Board