-
ID
#31404884 -
Job type
Contract -
Salary
BASED ON EXPERIENCE -
Source
Alpha Consulting Corp. -
Date
2022-01-12 -
Deadline
2022-03-13
Clinical Project Manager
California, Irvine, 92602 Irvine USAContract
Vacancy expired!
CLINICAL PROJECT MANAGER IRVINE, CARemoteProject 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.
- 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).
Vacancy expired!
Report job