Manager, Clinical Affairs and Regulatory Submissions |
| Summary:
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Supports the Director of Clinical Affairs and the company in the design, initiation, ... |
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CLINICAL RESEARCH SPECIALIST/ CLINICAL RESEARCH ASSOCIATE |
| A World Leader in Medical Technology is seeking a Clinical Research Associate to work an in-house ... |
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Sr. Project Manager |
| Our client is an innovative, research-based global pharmaceutical company whose research and ... |
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Clinical Project Assistant |
| Contract Clinical Project assistant in Irvine, CA.
Provide Administrative assistance in ... |
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Senior Software Engineer |
| Job Description: PRIMARY FUNCTION: Designs, develops and tests Windows Desktop Applications with a ... |
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Clinical Study Coordinator |
| The Clinical Study Coordinator will be the main point of contact for the clinic, sponsor and C... |
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Quality Control Technician |
| Levlad is a manufacturing company in servicing the beauty industry. We produce, package and ... |
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Medical Science Liaison - Western US |
| SOS provides various medical affairs functions to the pharmaceutical industry. SOS deploys M... |
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Quality Control Supervisor |
| Levlad is a manufacturing company in servicing the beauty Industry. Levlad produces, packages ... |
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Director, Clinical Development |
| Director, Clinical Development
Company:
Allergan
Location:
Irvine,?CA?92612
Status:
Full T... |
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Project Manager - Tustin, CA
| Details |
Country: USA
Location: CA Tustin
Total applied: 9
Job Type: Employee
Job Status: Full Time
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Project Manager - Tustin, CA
Project Manager
Tustin, CA
Direct-Hire
Our client, a premier Contract Research Organization (CRO) for clinical trials in the cardiovascular and metabolic disease areas, is seeking a Project Manager for a direct-hire position in Tustin, CA.
Responsibilities
The successful candidate will be responsible for facilitation, collaboration and management of one or more cross-functional project teams, in accordance with study expectations within the designated work scope, both internally and externally. Strong leadership skills, demonstrated project management abilities, and a service-oriented attitude interacting with all team members, both internally and externally required. The PM manages the overall operation of the clinical study, including: project planning, resource management, critical thinking and analysis of study metrics, study variance tracking; and problem-solving proactively in order to achieve work scope objectives and timelines within a project.
Qualifications
A Bachelor?s Degree, preferably in life sciences is required, along with 5+ years experience in the pharmaceutical industry.A minimum of 3 years experience as a CRA preferred (i.e., site monitor). Lead CRA activities within a study project preferred.
Metropolitan Research Associates is a full service CRO and clinical research staffing firm that offers expertise in all areas of clinical development for the pharmaceutical, biotech, and medical device industries.
We offer a very competitive salary and benefit packages. For more information about our job opportunities and MRA or to submit your resume, visit us at www.metropolitanresearch.com or fax to 919-510-7914.
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