*K Sample Management CoordinatorAt — Altasciences

Ensure the confidentiality of clinical trial participants and
sponsors is respected.
\uf0b7 Maintain and advocate a high level of customer service
and quality within the department.
\uf0b7 Report procedural deviations to appropriate supervisory
team members.
\uf0b7 Understand protocol driven timed study events and
acceptable windows (protocol and/or SOP driven) for the
timed events.
\uf0b7 Perform clinical trial activities which may include but not
limited to, tube/aliquot preparation, sample
handling/processing, sample inventory, and shipping.
\uf0b7 Ensure study specific sample management procedures are
executed when handling biological samples.
\uf0b7 Maintain equipment used in sample management (i.e.
freezers, refrigerators, centrifuges) and document
accordingly.
\uf0b7 Coordinate with external vendors (i.e. shipment couriers,
central lab).
\uf0b7 Maintain a continuous line of communication with
clinical/study operations teams on sample management
statuses.
\uf0b7 Act as a liaison to the clinical/study operations teams.
\uf0b7 Assist in the resolution of data queries.
\uf0b7 Generate and distribute sample management reports.
\uf0b7 Proactively communicate issues and/or problem
resolutions to departmental supervisors and managers.
\uf0b7 Complete and/or maintain training as required per jobs
needs.
\uf0b7 Perform general administrative tasks when required.

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Performance of clinical sample processing, relate topics learned to study drug effects, feel confident with public speaking skills.

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training:

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General employer orientation, as needed training for clinical sample processing, weekly one-on-one meetings with mentor to cover upcoming tasks, public speaking hours, and testing.

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Learning outcomes:

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Prioritize tasks in a fast paced and high workload environment.

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Communicate clearly and efficiently of completed or priority tasks.

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Work well in a team environment and also in an independent environment.