Research Associate Certified Phlebotomy Technician (evening shift)

Parexel

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profile Job Location:

Glendale, WI - USA

profile Hourly Salary: $ 20 - 26
Posted on: 18 hours ago
Vacancies: 1 Vacancy

Job Summary

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.

Job Title: Research Associate - Certified Phlebotomy Technician License Required

Shift: evening

Work Location: onsite in Glendale CA

Parexel Early Phase Clinical Unitsupports the development of innovative new medicines which are vital for public health improving outcomes and saving lives. The early phase and first in human trials are the first step in testing these novel treatments in humans.

At Parexel Glendale CA unit our highly trained and skilled Research Associates are crucial to ensuring the successful completion of Phase I trials. This is a great role for anyone that aspires to be an enrollment specialist clinical research coordinator or eventually manager. Parexel provides a great system of support to help you grow and advance your career internally.

Parexel comes along with anextensive induction program and ongoing training while following your individual career path.

What youll do after training is completed(including but not limited):

  • You will understand study protocols and be able to complete required medical procedures.

  • Recruit study participants by calling the database attending company sponsored community events posting flyers in schools senior centers supermarkets and other establishments.

  • Enter study participants in the study participant tracking system and study logs maintain appointment calendars and operate company information systems and computer programs.

  • Conduct screening visits and study protocol specific study participant visits assist staff physicians in assessment of concomitant medications adverse events lab results and other test results.

  • Prepare/monitor study supplies and stock levels in clinic/hospital.

  • Label inventory and send plasma samples.

  • Problem solves study participant issues as they arise.

  • Ensure basic study participant safety is provided.

  • Assist with Monitor visits (i.e. room set up etc.).

  • Identify issues that need Sponsor approval and bring these to the attention of the CRC.

  • Maintain and update knowledge of Clinical Operating Guidelines and their proper application.

  • Assume appropriate role with study participants and caregivers.

  • Assure quality and accuracy of source and CRF documentation.

  • Comply with Quality Management (QM) department guidelines and perform corrections for QM CRC and Monitor/Sponsor Representative in a timely manner.

Your Profile:

  • Active CPT License in the state of CA is required

  • Customer service experience in a fast-paced environment

  • Experience working in a medical or clinical setting is highly preferred

  • Comfortable standing and walking for a prolonged period of time

  • B.S. in related life science field OR HS diploma/GED with relevant experience

Hours/Shift - all shifts are onsite (no remote work)

  • Required Training: three weeks working 40 hours a week Mon - Fri 8:00am to 4:30pm then will move to PM shift training

  • Post training: Schedule will be shift start from 3pm for 8-hour shifts (3 weekend shifts in a 6-week period)

Base Pay Range: $20.00 to $26.00 per hour (this role is eligible for shift differentials)

Actual salaries may vary within the range based on several factors including but not limited to education training experience professional achievement and location.

In addition to base salary some roles may be eligible for participation in Parexels annual performance-based bonus plan annual salary review and additional total rewards incentives.

Our talent acquisition team will provide additional details on our bonus plan or incentive programs for those eligible roles. For all eligible employees we offer market leading benefit programs including paid time off 401k match life insurance health insurance and other benefit offerings in accordance with the terms of applicable plans.

EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status which in the US includes race color religion sex sexual orientation gender identity national origin disability or protected veteran status.


Required Experience:

IC

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...
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Key Skills

  • Laboratory Experience
  • Public Relations
  • Clinical Laboratory Experience
  • Classroom Experience
  • Ellucian
  • Physical Examinations
  • Phlebotomy
  • Bus Driving
  • Medical Terminology
  • CPT Coding
  • Patient Service Experience
  • Venipuncture Experience

About Company

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Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our the ... View more

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