Phlebotomist - Part time (M-F, (5 days per week, approximately 4 hrs/day (20hrs/week)

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<strong>Position : Phlebotomist - Part time (M-F, 4 hours per day, but flexible)<br><br></strong><strong>Location : San Jose, CA<br><br></strong><strong>Duration : 12 Months<br><br></strong><strong>Total Hours/week : 40.00<br><br></strong><strong>1st Shift<br><br></strong><strong>Client: Medical Device Company<br><br></strong><strong>Job Category: Medical / Clinical Affairs<br><br></strong><strong>Level of Experience: Entry Level<br><br></strong><strong>Employment Type: Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT)<br><br></strong><strong>Job Description<br><br></strong><ul><li>A copy of the license must be attached to the resume. License must be valid!</li><li>Phlebotomist (5 days per week, approximately 4 hrs/day (20hrs/week), with availability for periodic full 1 week (25-30hrs) coverage</li><li>Under supervision of a Licensed Phlebotomist or Licensed Medical Doctor and according to internal standard operating procedures, the associate will obtain specimens by venipuncture for the Associate Sample Collection Program (ASCP), perform documentation of daily draws utilizing required databases, contact internal donors, clarify internal collection requests, maintain inventory of phlebotomy supplies and a clean and orderly work environment.<br><br></li></ul><strong>Qualifications<br><br></strong><ul><li>Valid phlebotomy license, CPT-1 or CPT-2</li><li>1 year lab experience/blood draw preferred</li><li>Bachelor’s degree in a scientific discipline a plus</li><li>Proof of Hepatitis B vaccination or titer</li><li>Current certificate in adult basic life support (CPR)</li><li>Valid Driver’s License and reliable transportation</li><li>Experience and understanding of ethical and scientific quality standards for the design, conduct, recording and reporting of clinical research involving the participation of human subjects; including, but not limited to compliance with Good Documentation Practices (GDP), and Good Clinical Research Practice (GCP) to provide assurance that rights, safety, and well-being of research subjects are protected and respected</li><li>Must be able to work on site in client San Jose campus beginning at 8:00am</li><li>Interpersonal skills necessary to communicate effectively</li><li>Strong time management and multi-tasking skills, attention to detail</li><li>Ability to learn and utilize required databases and various software packages</li><li>Must effectively read, write, and verbally communicate in English</li><li>Ability to demonstrate strong teamwork, communication skills</li><li>Must have a drug test and background cleared before the worker begins the assignment .</li></ul>

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