Implementation Consultant

Implementation Consultant

Role Description & Responsibilities

• 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.
• Prior services delivery experience required
• 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.