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Bring your best skills forward to excel in the role:

- 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

Key Responsibilities:

- Requirements gathering and defining acceptance criteria, to align with the organization's specific needs and business processes.

- Ensuring data integrity and efficient workflows.

- Ability to provide insightful, deal-relevant points of view and recommendations based on robust analysis.

- System documentation as per GxP-compliant SDLC process

- Deliver end-user support, training, and change management to ensure successful technology adoption.

- Monitor platform updates and manage system upgrades or enhancements as needed.

- Ensure alignment with industry best practices and regulatory expectations for technology enablement in R&D.;

Read more about us:

- Recent Blogs

Job Location: Mexico City or Monterrey

Qualifications:

- Bachelor's degree mandatory. Desirable MBA or equivalent Masters degree in science, or a postgraduate degree with rich and relevant industry experience.

- 4+ years of progressive experience in the Life Sciences industry or consulting, ideally in roles involving business strategy systems implementation or technology transformation.





- Proven experience leading initiatives around Clinical trial systems, Regulatory submission tech, Patient safety reporting platform, and any modern tech solutions to accelerate Drug development space.

- 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).

- Extensive knowledge and experience in agile methodology-based technology transformation projects.

- 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.

- Advanced English is mandatory.

- Availability to travel may be required.

Good to have:

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

Additional Information:

Relocation Options: Candidates based in cities other than Mexico City or Monterrey can be considered, but Accenture regrets it does not cover relocation expenses for this position.

International Considerations: Foreign candidates can be considered but Accenture regrets that it is unable to sponsor employment Visas for this position.

#LI-LATAM

📌 Life Sciences R&D Consultant/Manager (México)
🏢 Accenture
📍 México