Thursday, 3 May 2012

SAP Jobs Need Project Manager with Research & Development, Rockville, MD

Hi,

We have an urgent requirement for Project Manager with Research & Development, Rockville, MD


Job Title

Project Manager with Research and Development

Experience Level

5 to 7 years

Location

Rockville, MD

Start Date

ASAP

Duration

6 – 8 months

Pay Rate

DOE

Job Description

 

Candidates need to be experinced in areas of Research and Development in aiding with Business Application Services.

 

ROLES & RESPONSIBILITIES:

·         Directly manages all aspects of the project life cycle and works with matrix IT partners to oversee all system development life cycle (SDLC) phases of a project.

·         Rigorously manages priorities and scope to ensure commitments are achieved within agreed upon time, cost, and quality parameters.

·         Develops communication plans and interfaces to execute on responsibilities.

·         Ensures that the project is executed and managed according to Client's Standard Operating Procedures, Working Practices, processes and tools.

·         Escalate unresolved issues to the project Lead, and Steering Committee leadership.

·         Identify, track, and resolve project issues in a timely fashion.

·         Develops the project charter, integrated project plan, resource plan, risk plan, and related project management artifacts.

·         Publishes periodic project status reports.

·         Manages the project change control process.

 

MUST HAVE SKILLS:

·         Demonstrated 5 - 7 years of Project Management experience in Life Sciences managing cross functional and/or global projects from beginning to end.

·         Knowledge of the Life Sciences industry in the context of applying information technology and services.

·         Knowledge of system development lifecycles (SDLC) with general understanding in the areas of application development, database, and system design.

·         Strong Vendor Management and Business Liaison skills

·         Knowledge of regulated environments, FDA regulations, including 21 CFR Part 11, quality standards, validation lifecycles, ICH guidelines, including GCP, GLP and GAMP.

·         Experience with the Pharmaceutical industry computerized system solutions in general (Clinical Trial Management, Regulatory Submissions, Data Management, and Clinical Safety preferred.

 



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Regards

Alex Hunt
Talent Acquisition

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