Sr. Clinical Project Manager (Real Life Sciences)

Clinical Research Universe Featured Jobs

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
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T: +1 619 881 0004
E: r.brown@realstaffing.com

Associate Director/Director (Aerotek)

Clinical Research Universe Featured Jobs

Posted: October 3, 2016

Job ID: 165

Job Summary

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

Job Description

Title: Associate Director/Director (depending on experience)
Company: Small Biotech
Location: San Diego, CA (must work in the office)
Target Salary: TBD
Travel: Very limited
Requirements: 8+ years of experience in clinical research. Will look at candidates at the Sr. Project/Trial Management level who are ready to take the next step. Must have experience working on EU trials. Ideally candidates will have experience at both a CRO and a small sponsor company. Must have experience with Phases I-IV and have the ability to lead a team.

Please contact:
Morgan McCormick
SR. ACCOUNT RECRUITING MANAGER
RECRUITER LEAD
CLINICAL DIVISION
(858) 609-2019 Phone

ACRP Training: Project Management for Clinical Research Professionals

ACRP is offering a course in project management for clinical research professionals. This is a 2-day course specifically designed for clinical research project management and will help you gain a broader perspective of the clinical trial lifecycle.

It is $645 for ACRP Members with Early-Bird Pricing.

Research Triangle Park, NC (July 14-15)
Seattle, WA (September 8-9)
Arlington, VA (November 3-4)

ACRP Training and Development: Project Management for Clinical Research Professionals

This 2-day live course provides detailed, practical guidance on the project management skills used by effective study sponsors and contract research organizations and how to apply them in your trials.

Specifically designed for clinical research project management, this course will help you gain a broader perspective of the clinical trial lifecycle – and increase productivity and revenue – through examples and exercises developed from real-world pharmaceutical research scenarios.

If interested, please click here: