Jaime Flowers, Pharm.D. Email & Phone Number

Memphis, Tennessee, Us

• Lead the development of oncology medical letters and responses to escalations frominternal and external stakeholders• Collaborate cross functionally (e.g. marketing, communications agencies, medical,regulatory) as a medical information reviewer providing solutions, providing guidanceand insights on medical and commercial materials• Ensure accuracy, scientific balance and fair-balance of medical and commercialmaterials• Generate and review insight reports to identify and analyze trends that inform thecreation/update of medical affairs deliverables• Influence the design of an AI tool by user testing and analysis providing feedback onaccuracy, quality, formatting and performance enhancements

Memphis, Tennessee, Us

• Serve as medical information subject-matter expert for assigned product• Provide strategic medical and scientific insight to commercial partners for sales aids, slide decks, websites, social media, and sales training• Serve as lead medical information reviewer on the medical legal regulatory review team• Lead strategy for development and/or review of medical information deliverables (e.g., standard response documents, custom responses, slide decks, and dossiers) • Provide insight on omnichannel marketing of a medical information digital capability• Performed user testing of an AI tool designed for clinical content creation; analyzedoutput and provided feedback to the development team to inform the selection of an AI tool• Demonstrate ongoing scientific expertise relevant to assigned product• Comply with all guidelines, policies, legal, regulatory, and compliance requirements.• Lead the handling of compendium review requests for assigned product

Memphis, Tennessee, Us

• Create custom responses to unsolicited medical information inquiries• Create and review standard responses for unsolicited medical information inquiries• Provide consultation and review of promotional materials• Assist in training of new team members

Memphis, Tennessee, Us

•Lead a team of seven US and OUS medical information specialists providing on average of 50- 70 responses a day• Monitor team workload by performing daily and weekly case reviews to check adherence to work instructions and conformance to process change • Assess the complexity of cases and provide guidance to the team on case handling• Foster relationships with team members to educate and empower them to handle complex cases• Serve as a liaison between the client and Med Communications• Facilitate meetings with client cross-functional teams (e.g. Pharmacovigilance, Quality, Medical Information) to assess needs, receive client communications and feedback on cases• Identify cross-functional team needs and determine how the needs can be met• Collaborate with cross-functional teams to increase team efficiency in providing information • Identify strategy for implementation of process changes• Lead team in execution of process changes • Lead weekly meetings to provide recognition, share best practices, share client communications, and address questions• Act as resource to internal customers for knowledge of client processes

Lake Mary, Fl, Us

• Lead pharmacy teams of 3 to 6 people daily; at times in different locations, to deliver high quality customer service • Using clinical analytics, lead medication therapy management to drive adherence to evidence based medicine guidelines• Reviewed prescriber-specific opportunities to improve care on behalf of patients• Engaged prescribers and nurses through telephonic outreach or fax to improve medication compliance and promote cost-effective prescribing behavior• Reviewed patient-specific opportunities to optimize and provide cost-effective, quality care

Indianapolis, Indiana, Us

• Provided vendor oversight on the creation and update of global response documents (GRDs)• Organized and developed the training program for affiliate medical information colleagues• Contributed to cross-functional team projects• Precepted pharmacy students• Conducted pharmacy resident training• Leveraged expertise to enhance and broaden knowledge of field medical team colleagues by training on primary literature evaluation

Indianapolis, Indiana, Us

• Partnered with my team to develop and maintain the oncology portfolio of GRDS• Independently managed a portfolio of close to 50 GRDs for Gemzar and Alimta• Performed literature searches, evaluated the primary literature, and incorporated information from medical meetings to provide timely updates to GRDs. • Collaborated with medical affairs colleagues to create Gemzar and Alimta GRDs• Participated in pre-launch strategy discussions with cross-functional colleagues and gained insights to identify Alimta GRD topics • Leveraged positive relationships formed with clinical research physicians and members of data management, regulatory, pharmacokinetics and manufacturing to aid in timely responses to ad-hoc requests from global medical information affiliates• Engaged KOLs and other HCPs at medical/scientific meetings

Wilmington, Nc, Us

Durham, North Carolina, Us

Chapel Hill, Nc, Us