Life Sciences R&D Consultant/Manager

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Overview

Join Our Global Consulting Network and Expand Your Horizons! Are you ready to take your career to new heights? At the Global Network,

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OtherConsultant

Are you ready to take your career to new heights? At the Global Network, we are more than just a team; we are a thriving community of over 10,000 professionals operating from key locations around the world. We specialize in providing top-tier consulting expertise across various industries and functional areas, including life sciences, energy, supply chain operations, finance, and talent management.

Deep understanding of Life Sciences/BioPharma R&D processes.
Familiarity with clinical trial systems, regulatory submission tech, patient safety reporting platform, and any modern tech solutions to accelerate drug development.
Strong stakeholder engagement and team leadership capabilities.
Ability to develop strategic perspectives and thought leadership on industry trends, digital transformation, and innovation in R&D.
Excellent communication, interpersonal, and analytical problem-solving skills

Responsibilities

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Requirements gathering and defining acceptance criteria, to align with the organization's specific needs and business processes.
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Ensuring data integrity and efficient workflows.
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Ability to provide insightful, deal-relevant points of view and recommendations based on robust analysis.
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System documentation as per GxP-compliant SDLC process
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Deliver end-user support, training, and change management to ensure successful technology adoption.
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Monitor platform updates and manage system upgrades or enhancements as needed.
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Ensure alignment with industry best practices and regulatory expectations for technology enablement in R&D.

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Requirements

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In-depth understanding of Life Sciences R&D functions including Clinical Operations, Regulatory Affairs, Quality Assurance, Safety, and related compliance requirements (GxP, 21 CFR Part 11).

Demonstrated ability to manage multiple concurrent projects, prioritize tasks, and deliver outcomes in a fast-paced environment with multiple stakeholders.

Proven ability to effectively plan, manage, and coordinate multiple projects in a dynamic environment with numerous and complex stakeholder groups.

Excellent documentation skills and exposure to work within GxP-validated systems.

Experience in at least 4-5 of the following areas:

Clinical Trial Management Systems (CTMS)
Regulatory Information Management (RIM)
Electronic Trial Master File (eTMF) or Clinical Document Management
Clinical Data Management / EDC
Biostatistics or Clinical Data AnalyticsLaboratory Information Management Systems (LIMS)
Quality Management Systems (QMS)
Pharmacovigilance or Safety Systems

Accenture is a leading global professional services company that helps the world’s leading businesses, governments and other organizations build their digital core, optimize their operations, accelerate revenue growth and enhance citizen services—creating tangible value at speed and scale. We are a talent- and innovation-led company with approximately 791,000 people serving clients in more than 120 countries. Technology is at the core of change today, and we are one of the world’s leaders in helping drive that change, with strong ecosystem relationships. We combine our strength in technology and leadership in cloud, data and AI with unmatched industry experience, functional expertise and global delivery capability. Our broad range of services, solutions and assets across Strategy & Consulting, Technology, Operations, Industry X and Song, together with our culture of shared success and commitment to creating 360° value, enable us to help our clients reinvent and build trusted, lasting relationships. We measure our success by the 360° value we create for our clients, each other, our shareholders, partners and communities.

Visit us at www.accenture.com

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