Clinical Project Manager
Location: North Chicago Illinois
Description: Collabera is currently seeking to employ Clinical Project Manager right now, this job will be placed in Illinois. More details about this job opportunity please read the description below. Required Skills
:
Bachelors Degree in Science, Business Administration or equivalent . 0 - 3+ years total experience in the Pharmaceutical Industry. Must have experience as one of the following:
- Scientist / Senior Scientist
- Staff / Clinical Research Pharmacist,
- Clinical Project Manager or Clinical Research Manager Associate
- Clinical Supply Project Manager, Consultant, Coordinator or Associate.
- Analyst/formulator/process development specialist
- Active pharmaceutical ingredient project manager
- Manufac! turing operations project/program manager
- Quality Ass! urance role
- 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 creating appropriate protocol specific manufacturing and packaging work orders in concert with Third Party and IVRS vendors, QA, clinical team partners etc to ensure timely availability of clinical supplies.
- Responsible for protocol specific clinical su! pplies scenario analysis, risk management and contingency planning. Forecasts protocol specific bulk drug product requirements, including comparator agents, ancillary supplies and commodities, including overages.
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Pharmaceutical
Location
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North Chicago, Illinois, US
Posting Start Date
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Posting End Date
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Pay rate
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DOE
Duration
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1 Year
DESCRIPTION
Manage Phases I â€" IV domestic and international clinical research studies. Responsibilities include protocol design and development, case report form development, contract negotiation, site recruitment, support program management for project reviews, budget and timeline development, establish relationships with outside vendors, medical consultants and partners, provide IND and NDA summary reports, interface with interdisciplinary teams, monitor project timelines, develop ! project management tools, and provide project presentations. 0-3 Years ! Experience Level.
REQUIREMENTS
Education
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Experience
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1 - > 25 years
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If you were eligible to this job, please email us your resume, with salary requirements and a resume to Collabera.
If you interested on this job just click on the Apply button, you will be redirected to the official website
This job starts available on: Sat, 14 Dec 2013 00:33:56 GMT