Associate System Set-Up Analyst

2 weeks ago


Bengaluru, Karnataka, India Parexel Full time

When our values align, there's no limit to what we can achieve.

The Associate System Set-up Analyst (aSSA) ensures the technology set-up at a clinical trial's outset supports the profitability of the trial, ensures quality delivery, and maximizes the efficiency of operational resources assigned to the trial. For assigned trials, the aSSA has responsibility for the configuration of system set-up. The Associate System Set-up Analyst may be responsible for the validation documents of vendor system configuration.

Key Accountabilities:

Project Delivery

Set-up trial technologies. Ensure the quality, timeline and budget related to the trial technology meets the project requirements. Create documentation to validate vendor system configuration. Stay current on the latest Parexel technology offerings, integration issues, and relevant clinical trial process developments in the industry.

General Administration

Maintain a positive, results oriented work environment, modeling teamwork, and communicating with team members in an open, balanced, and objective manner. Maintain a working knowledge of applicable ICH Guidelines and Good Clinical Practices. Complete routine administrative tasks in a timely manner (e.g., timesheets, training) and in compliance with relevant guidelines.

Skills:

Ability to resolve issues independently with good judgement to escalate appropriately. Experience in clinical trial systems (e.g., CTMS, EDC, RTSM) with detailed understanding of requirements gathering, documentation, configuration, and integrations. Ability to learn new systems and integration requirements. Strong interpersonal, verbal, and written communication skills. Knowledgeable in ICH and GCP regulations in relevant geographies

Knowledge and Experience:

Fluent in written and oral English and local language. Knowledge in clinical research industry, including detailed understanding of clinical technology, design, and system requirements. Work experience in a CRO/Pharma setting (operational or technical). eCOA, ePRO experience is a plus.

Education:

Educated to degree level in life sciences and/or computer sciences or other equivalent experience.

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