Regulatory Associate in King of Prussia, PA |
| Smith Hanley is in search of 2 Regulatory Associates in King of Prussia, PA Regulatory A... |
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Sales Specialist |
| SALES SPECIALIST
Join a fast growing water treatment company in the Phila area who has an opening ... |
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HPLC Specialist - Technical Support |
| System One is presently seeking candidates for a HPLC Specialist - Technical Support opportunity ... |
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Channel Implementation Lead |
| At GlaxoSmithKline, our goal is simple: to improve the quality of human life by enabling people to ... |
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Production Worker |
| Peopleshare is seeking for Candidates to work for a great company in Exton to monitor a label ... |
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Director of Clinical Operations |
| Full Time, Temporary/Contract/Project, Employee Job Category: Biotech/R&D/S... |
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Product Specialist/Health & Wellness Industry |
| Title: Product Specialist
Location: Philadelphia Area
Job Description:
Our client, the nation's ... |
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Clinical Affairs Group Manager |
| Position provides coordination, execution, and completion of high quality, Class III medical device ... |
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Regulatroy Affairs Group Manager |
| The Group Manager, Regulatory Affairs, is responsible for writing, submitting and gaining approval ... |
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Project Manager (Phase I experience) |
| Premier Research is a leading solutions-driven CRO leveraging our commitment to therapeutic focus ... |
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Study Coordinator/Clinical Research Associate
| Details |
Country: USA
Location: Pennsylvania-Philadelphia Jenkintown, PA 19046
Total applied: 27 Job Category:Biotech/R&D/Science
Relevant Work Experience:2+ to 5 Years
Location:Jenkintown, PA 19046
Status:Full Time, Employee
Occupations:Clinical Research;Pharmaceutical Research
Career Level:Experienced (Non-Manager)
Relevant Work Experience:2+ to 5 Years
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Study Coordinator/Clinical Research Associate
Clinical Research;Pharmaceutical Research Relevant Work Experience: 2+ to 5 Years Career Level: Experienced (Non-Manager) Job Description Immediate full-time opening for a dynamic, flexible individual to serve as a Clinical Research Associate/Study Coordinator in Jenkintown, PA diagnostic imaging center. We conduct Phase I - IV clinical research trials. Must be independent, motivated and computer savvy, with clinical trial experience in study management, regulatory submission and patient monitoring via CRFs. Responsibilities: - Coordinating protocols for sponsor initiated pharmaceutical studies under the supervision of the site director and the principal investigator. - Creates accurate patient charts, records, source documents and CRF pages. - Perform testing procedures per protocol including ECGs, drawing labs - Attends investigator meetings. Also attending site initiation visits and monitoring visits. - Conducts clinical research according to GCPs, FDA regulations and imaging center's SOPs Required: - Experience with sponsor initiated clinical trials - Detail oriented with strong organizational skills - Experience with subject recruitment - Perform MA (medical assistant) duties including: vital signs; draw blood, EKGs etc - Knowledge and understanding of GCP, HIPPA and FDA Regulations. - Excellent interpersonal, oral and written communication skills. - Experience in electronic data transfer, query resolution and SAE reporting. Contact InformationName:
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