Clinical Project Manager

Clinical Project Manager

07 Jan 2024
California, Irvine, 92602 Irvine USA

Clinical Project Manager

Vacancy expired!

CLINICAL PROJECT MANAGER
IRVINE, CARemote
Project Description:

  • Responsible for the project management of key Clinical Supply Chain activities at the protocol level for pre-clinical and Phase I - II clinical trials
  • Includes forecasting, planning, scheduling, coordination, and execution, ensuring timely availability of investigational drug supplies and related services to clinical sites and depots.
  • Provides input to Clinical Study Teams to influence clinical protocol design to ensure most efficient utilization of supply chain resources.
  • Translates clinical study design into packaging design. Authors the study medication and labeling section of the clinical protocol.
  • Develops protocol specific labeling compliant with applicable global regulations.
  • Identifies, develops, communicates, and tracks project timelines, activities, logistics, and milestones.
  • Responsible for protocol specific clinical supplies scenario analysis, risk management and contingency planning.
  • Forecasts protocol specific bulk drug product requirements, including comparator agents, ancillary supplies, and commodities, including overages.

Required Skills:
  • Education Requirement: Bachelor's Degree required preferably in physical science, math, engineering, or pharmacy.
  • Experience: 2+ years total experience in the Pharmaceutical Industry. Preferably experience in one of the following areas:
  • Drug discovery (eg, Process Chemistry, Analytical Chemistry)
  • Drug development (eg, Formulation)
  • Clinical operations (eg, Clinical Project Management)
  • Supply chain (eg, Clinical Supplies Project Management)
  • Quality Assurance
  • Understanding of clinical development and global supply chain requirements.
  • Competent in the application of standard business requirements (for example SOPs, Global Regulations).
  • Understanding the importance of compliance in a regulated environment and be capable of applying this knowledge to daily work.
  • Ability to work collaboratively within the dept as well as cross-functionally including interacting in a tactful, professional, and effective manner.
  • Ability to work effectively and professionally with those in the dept as well as Clinical, QA, Analytical and any area interface.
  • Ability to manage and prioritize multiple tasks.
  • Project Management skills.
  • Good communication skills (both written and oral).

This 6+ month position starts ASAP.

Please E-MAIL your resume (attachment to email) with rate and availability to Bridget:

ALPHA'S REQUIREMENT #21-04415
MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE
#LI-BB1

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Job Details

  • ID
    JC30264629
  • State
  • City
  • Job type
    Contract
  • Salary
    BASED ON EXPERIENCE
  • Hiring Company
    Alpha Consulting Corp.
  • Date
    2022-01-06
  • Deadline
    2022-03-07
  • Category

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