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DM Clinical Research

Pharmacist

Jersey City, NJ · On-site

$123K - $147K/yr

Pharmacist DM Clinical Research is looking for a Pharmacist to fill our Unblinded Clinical Research Coordinator role and join our team. This individual will be responsible for dispensing ...

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    Site System Associate II

    DM Clinical Research

    Houston, TX • On-site

    Full-time

    This job post has expired today. Applications are no longer accepted.

    Job description

    Site System Associate II
    The purpose of this position is to provide technical expertise and organize the support of the Site Systems such as eSource, eConsent, eRegulatory, Looker, etc..to all DM Clinical Research Sites. The incumbent will serve as the first point of contact for matters related to site systems. The incumbent will have to work closely with all branches of Central Services as well as other functional teams across DM Clinical Research. The incumbent may be involved in identifying and researching new tools/systems that may be useful for DM Clinical Research. The incumbent may also provide support during deployment based on Site System Manager guidance.
    DUTIES amp; RESPONSIBILITIES
    • Perform the development of each study into the electronic source, setting up new users and giving them access to the system based on set internal policies.
    • Perform finance configuration-related tasks based on departmental needs.
    • Act as the primary point of contact for any site system-related queries and questions
    • Contribute to the configuration, migration, User Acceptance Testing (UAT), validation, implementation, and maintenance of the eSource, eConsent, eRegulatory, Payment system, transportation system, looker, and any systems that come under Site Systems.
    • Collaborate with Clinical Operations Leadership on Super-User strategy to broaden end-user support and training.
    • Responsible for any special projects and tasks assigned by the manager or senior leadership.
    • Provide relevant audit support during inspections.
    • Identify opportunities for continuous process improvement; recommend solutions and implement them as needed
    • Any other matters as assigned by management

    KNOWLEDGE amp; EXPERIENCE
    Education:
    • BA/BS degree required
    Experience:
    • 6 month working experience required in site system OR candidate must have 2 year of Clinical Research work experience
    Credentials:
    • N/A
    Knowledge and Skills:
    • Knowledge of any following vendor system: eSource Design, transportation portal, eConsent portal
    • Ability to manage User management of vendor system on own
    • Ability to multitask, communicate with internal stakeholders and gather system requirements
    • Knowledge of general system workflows, GCP guidelines, ALCOA-C related to electronic systems in clinical research.

    Apply