Ref #: 29168

Employment type: Permanent - Full-Time

Location: United States - remote

Posted: 16-May-2021

Description

DOCS is searching for patient portal experts to global trials.


In this role you will support the creation,
management and retirement of study specific, site facing portals used to support engagement and
communications with Clinical Study site personnel. You will work with study team members to implement the study team’s engagement strategy, managing email communications, news posts, enrollment dashboards, visit guides and calculators, surveys and forms.
You are responsible for portal user management and the point of contact for vendor management.

Qualifications:

Experience with clinical trial coordination or clinical trial monitoring.
Experience working on a study with an Investigator Portal.
Experience working in highly diverse teams within clinical research; cross-functional, global, multi- regional.
Basic project management skills.
Experience with overseeing technical and system administration for portal or community
platform.
Bachelor’s degree or equivalent, in Health or Science discipline with experience in clinical
research.

DOCS is the FSP division of ICON Clinical Research. We provide global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry.


DOCS is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.

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