Procter & Gamble Pharmaceuticals Work Values

Daily Duties at Procter & Gamble Pharmaceuticals:

Plan, organize, and manage tasks related to the development of clinical and regulatory documents including Phase 1-4 protocols, clinical study reports, investigator brochures, informed consent forms, patient narratives, independent committee charters, briefing packages, INDs and updates, NDAs, and regulatory responses. Collaborate with multidisciplinary team members to develop and manage project timelines; ensure that timelines are met, and complete documents according to applicable regulations and guidances, ICH guidelines, GCPs, and P&G SOPs. Ensure consistency of documents within and across clinical programs by managing content and using document standards, styles, and templates. Participate in SOP development and review. Organize, integrate, summarize, and present scientific and clinical data and information from a variety of primary sources in an accurate, clear, concise, and consistent manner for a variety of audiences.

What they like about Procter & Gamble Pharmaceuticals:

You highly value a work environment built on a formal structure, rules, and regulations. You do not enjoy the unpredictability of shifting priorities and deadlines that upset your routine. You require and enjoy direction, input and accountability as part of your work environment. You have a strong need to participate in making key decisions and feel left out if your superiors or co-workers do not seek your input when making decisions. You thrive on providing good customer service to both internal or external customers, and doing so makes you feel good.

Tags

Regulatory Affairs, home based, PharmD, Word, Acrobat, Excel, eCTDXpress, OTCs, Medical Writing, Regulatory Strategy, Manager, Pharmaceuticals, Generics, INDs, NDAs, ANDAs, Clinical Development, clinical trial design, regulatory submissions, Phase 1-4, labeling, advertising, promotional materials, global, cross-functional team leader, ISI Toolbox, Documentum

Skills

regulatory strategy, regulatory submissions, communication, oral and written, people management, project management, medical writing, clinical trial design, protocol development, collaboration, creative problem solving, decision making, analytical assessment, MS Word, Adobe Acrobat, ISI Toolbox, eCTDXpress, MS Project, MS Powerpoint, Excel, Sharepoint, Documentum, grace under pressure, multitasking

These are some of the questions we asked our climbers about their experiences with Procter & Gamble Pharmaceuticals: