Laboratory Specialist Position Available In Pinellas, Florida

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Company:
Clinical Research Of West Florida
Salary:
$50000
JobFull-timeOnsite

Job Description

Laboratory Specialist Clinical Research of West Florida, Inc – 1.0 Clearwater, FL Job Details Full-time From $50,000 a year 1 day ago Benefits Health insurance 401(k) Paid time off Parental leave Professional development assistance Referral program Qualifications CPR Certification Microsoft Excel Microsoft Outlook Clinical research Phlebotomy BC/BE Laboratory experience Organizational skills Clinical trials Medical License Good Clinical Practice 1 year Entry level Full Job Description Interested in this job? Please submit your resume to Site Director (Clearwater Site). Please do not call the office regarding this job or for a status update. All qualified candidates will be contacted via phone call and email. Laboratory Specialist Clinical Research of West Florida, Inc. – Clearwater, FL Immediate full-time Laboratory Specialist position available for an individual who is detail-oriented, energetic, hardworking, efficient and willing to grow with the company. The Laboratory Specialist will be responsible for the collection, processing, and shipping of various biological samples as well as completing appropriate paperwork and documentation. Phlebotomy experience is required .

Responsibilities and skills needed:
  • Ability to handle blood, urine, stool, and various types of biological samples
  • Collect, process, and ship samples for clinical trial subject visits
  • Maintain daily temperature logs . Maintain protocol specific processing logs
  • Assist coordinators with subject visits and assessments (i.e., vitals, ECGs)
  • Prepare lab kits
  • Inventory of trial lab kits and breakdown of expired kits
  • Complete all study required trainings prior to working on clinical trial
  • Assist lab director with lab supply inventory
  • Attend SIVs and meet with monitors as required
  • Assist with other administrative tasks related to clinical trial conduct
  • A positive attitude and willingness to assist Study Coordinators with patient visits
  • Must be self-motivated and have a desire to learn
  • Meticulous attention to detail when filling out laboratory documents and logs
  • Great organizational skills and legible handwriting
  • Able to multi-task and follow detailed instructions
  • Maintain security and confidentiality of patient/sponsor information
Professional Requirements:
  • Maintain current medical licensure (if applicable)
  • Meet CEU requirements to keep licensure up to date
  • Maintain CPR certification
  • Maintain IATA/Biohazard Certification
Maintain GCP Certification Qualifications:

Must be able to comprehend complex protocols, work independently, manage multiple ongoing issues, and work in a dynamic/collaborative environment. Ability to communicate effectively with study participants, sponsors, and staff.

Phlebotomy:

1 year (Required)

Preferred Experience:

Clinical research related experience, GCP training, Office Word/Excel/Outlook, With multiple offices located in Clearwater and Tampa, CRWF is an industry leader in the field of clinical research. The company has facilitated more than 1000 Phase I-IV research studies in various therapeutic areas. CRWF is dedicated to providing excellent patient care and board certified/eligible physicians along with an experienced, highly trained clinical staff conduct our studies. EOE. Competitive Salary Package.

Job Type:
Full-time Pay:

From $50,000.00 per year

Benefits:

401(k) Health insurance Paid time off Parental leave Professional development assistance Referral program

Schedule:

Monday to

Friday Work Location:

In person

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