Chargement en cours

Consultant Cybersécurité - IAM

CHÂTILLON
il y a 1 jour

Industry knowledge of Clinical Trial processes, specifically as they relate to data collection, standards, management, and preparation for statistical analysis

Strong understanding of those associated specifications, and ability to translate them into clinical systems solutions

Ability to work with technical R&D staff and translate new software features into real world examples

Knowledge of computer usage in a web-based environment

Ability to absorb and apply new information quickly

Ability to think logically to solve complex problems

Solid analytical and technical skills with regard to software applications

Strong collaboration and team-building skills

Excellent verbal and written communication skills

Strong organizational and time management skills

Self-motivated, able to assume responsibility and work autonomously in a professional manner

Experience of working to Standard Operating Procedures

Adaptable to changing business needs and/or product landscapes

Willing to travel to office locations and customer engagements

Strong understanding of Clinical Study Setup activities within the Rave database.

Experience or basic knowledge of eCOA, Patient Cloud, and other Medidata-related products.

Fundamental understanding of Clinical Data Management (CDM) processes and workflows.

Qualifications

Minimum 4-year university/college degree or equivalent (analytic discipline a plus)

Experience working with clinical trials, or equivalent combination of education and experience required.

Strong understanding of Clinical Study Setup activities within the Rave database.

Experience or basic knowledge of eCOA, Patient Cloud, and other Medidata-related products.

Fundamental understanding of Clinical Data Management (CDM) processes and workflows.

Experience supporting project teams and meeting project timelines

Prior data management or clinical trial software consulting experience preferred.

Basic knowledge of clinical research concepts, study lifecycle, and regulatory expectations.

Ability to work in a client-facing role, including effective communication and requirement gathering.

Good problem-solving skills with the ability to analyze issues and provide timely resolutions.

Capability to collaborate with cross-functional teams such as CDM, clinical operations, developers, and QA.

Detail-oriented approach to ensure high-quality study build and timely delivery.

Ability to manage multiple tasks, prioritize effectively, and adhere to timelines.

Willingness to learn and adapt to evolving tools, processes, and client needs.

What’s in it for you?

Work in a culture of collaboration and innovation .

Get an understanding of the software architecture and interfaces of relevant in-house and

external software components.

Work together with the Product Owner to satisfy the stakeholders in the best way respecting their requirements and scope.

Ensure knowledge sharing within the development team and encourage introduction of new technologies.

Proactively optimize development processes and suggest new ideas.

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Entreprise
Metaline
Plateforme de publication
WHATJOBS
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