Sr. Clinical Project Manager (Real Life Sciences)

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Posted: October 3, 2016

Job ID: 166

Job Summary

Term: Full-Time
Job Roles: Trial/Study Management, Project Management
Required Experience: 4+ years

Job Description

Below are the relevant details of the position for you to review, please pass along an updated resume and time your available to go over details to see if it's going to be a good fit with your background.
Responsible and accountable for several clinical trials.
Facilitate investigational site budget negotiations.
Manages each project within agreed upon timelines.
Provides regular updates to the staff, Sponsor, vendors and contract staff concerning status and progress of the trial.
Facilitate protocol and related document development.
Responsible for writing/approving clinical project deliverables such as scope definition documents, CRFs, source documents, monitoring tools, monitoring plans, close-out plans.
Responsible for ensuring the trial is “audit ready” at all times (project team training records, current regulatory documents, appropriate IRB approvals, monitoring tools required for the trial). Ensures that any audit observations are addressed appropriately and in a timely manner.
Coordination/execution of all operational aspects of clinical studies (including identification and management of vendors, availability of clinical supplies at the sites, review and approval of request for investigational test articles).
Assist with training and supervising junior level CRAs.
Best Regards,

Rebecca Brown

Real Life Sciences
Desk Hub, 2159 India Street, Suite 200, San Diego, CA, 92101, United States
T: +1 619 881 0004