4.0 - 9.0 years

4 - 9 Lacs

Hyderabad, Telangana, India

On-site

The overall purpose and main responsibilitiesare listed below: Tocreate complex and specialized content without supervision; manage end-to-end publication/medical education content development process including documentation and approval inPromoMats/iEnvision(previously-Datavision/MATRIX); develop andmaintaintherapeutic areaexpertise;coach andreview content created by junior scientific writers; work in close collaboration with peers/team to develop best practices; and collaborate effectively withstakeholders People: (1)Maintain effective relationship with the end stakeholders (medical scientific community) within the allocatedGlobalBusiness Unitand product - with an end objective to develop education and communication content as per requirement;(2)Interact effectively with health care professionals on publication content; and (3)Constantly assistjuniorwriters in developing knowledge and sharing expertise Performance: (1)Provide publication/medical education material (slide deck, abstract, poster, manuscript etc.) as per agreed timelines and qualityand (2)Provide strategic support with individuals and institutions, which may serve as resources for publications purpose Process: (1)Develop complex publication/medical education material; (2)Support medical communication and develop subject matter expertise for the assigned therapeutic area(s); (3)Assist the assigned scientific communication team in conducting comprehensive publication-need analysis; (4)Implement the publication plan and associated activities for the year identified for the region; (5)Work with selected vendors within the region to deliver the required deliverables as per defined process; (6)Leverage advanced training delivery tools and techniques thereby enhancing the effectiveness of training delivery; and (7)Design an overall plan of action based on end-user feedback and improve course content and delivery Stakeholder: (1)Work closely with scientific communication teams in regions/areas toidentifypublication need andassistin developing assigned deliverablesand (2)Liaise with medical department to prepare relevant and customized deliverables About you Experience :>4years of experience in content creation for the pharmaceutical/healthcare industry, or academia Softskills :Stakeholder management;communication skills;andability to work independently and within a team environment Technical skills :As applicable(including but not limited totherapeutic area/domainknowledge exposure;publication submission; and/or project management) Education :Advanced degree in life sciences/pharmacy/similar discipline or medical degree Languages :Excellent knowledge of English language (spoken andwritten)

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Senior Consultant Deloitte Consulting

6.0 - 9.0 years

16 - 22 Lacs

Bengaluru

Hybrid

Job Description: We are seeking an experienced Veeva Vault professional with a strong background in the life sciences domain to support and lead configuration, implementation, and enhancement activities across Veeva Vault applications. The ideal candidate will serve as a subject matter expert (SME), ensuring all platform decisions align with enterprise architecture and compliance frameworks. Key Responsibilities: Lead the implementation, configuration, and continuous improvement of Veeva Vault applications (any Vault QMS, RIM, PromoMats, etc.). Act as the primary technical point of contact for Veeva Vault platform initiatives, managing end-to-end delivery of configuration tasks. Ensure configuration decisions align with the clients enterprise architecture, data governance, and document management best practices. Collaborate with cross-functional teams (QA, RA, IT, Validation, Business Functions) to elicit, analyze, and translate requirements into scalable Vault configurations. Review and approve configuration changes and customizations to ensure optimal performance, regulatory compliance, and long-term scalability. Govern configuration management practices to maintain system traceability, version control, and adherence to Veeva best practices. Perform impact assessments for proposed system enhancements, focusing on long-term maintainability, audit readiness, and validation implications. Support validation lifecycle activities, including drafting/reviewing configuration specifications, risk assessments, and test protocols (IQ/OQ/PQ). Troubleshoot system issues and coordinate with Veeva support and internal IT teams for timely resolution. Provide SME-level input during integration efforts with enterprise platforms such as RIM, QMS, ERP, and other regulated systems. Mentor and support business users, administrators, and project teams in leveraging Vault capabilities and ensuring adherence to document/data lifecycle governance. Lead and manage Release Impact Assessments (RIA) for each major Veeva Vault release in the context of live applications. Qualifications: Bachelor’s or master’s degree . Minimum of 6 years of hands-on experience in the life sciences domain with expertise in configuring and managing Veeva Vault solutions. Strong understanding of GxP, validation principles, and document/data governance standards. Excellent problem-solving, communication, and stakeholder management skills. Proven experience with system integrations and cross-platform configuration strategies. Veeva Vault certifications (preferred but not mandatory).

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