Clinical Research Associate II

Job ID
48240
Department
Pharmaceutical Sciences
Category
Clinical Trials
Job Location
US-TN-Memphis

Overview

As a Clinical Research Associate II in the pharmacokinetic (PK) study lab, you are responsible for communicating with collaborating sites to manage shipment of supplies, collection of samples, and obtaining all necessary clinical information. Acting as a study coordinator, you ensure the mandatory PK studies in the brain tumor program are both implemented and performed correctly. The studies are not only growing in complexity, but also they are growing by adding new participating sites. Primary responsibilities include:

  • Communicating with study team members about scheduling PK study appointments in the clinic
  • Accessioning samples from the clinical lab
  • Gathering necessary information about samples and entering data into relevant databases
  • Providing data reports to CRO, study sponsors and/or principle investigators
  • Develop and monitor PK data collection forms and related documents

Take the first step to join our team by applying now!

Responsibilities

As a Clinical Research Associate II, your role will also entail:

  • Operates under general supervision.
  • Performs activities consistent with those of a Study Coordinator role such as maintenance of protocol portfolio(s), informed consent(s), and preparation/submission of complex study documents.
  • Performs data abstraction, collection, and entry to support clinical research.
  • Prepares submission for all reportable events.
  • Develops, maintains, and/or monitors case report forms.
  • Ensures compliance with prescribed interventions and evaluations of the assigned protocol(s).
  • Provides data to the collaborating research organization or study sponsor.
  • Prepares complex data reports.
  • Serves as a mentor and preceptor to staff.

Minimum Education

  • Bachelor's degree in a related biomedical/bio-behavioral field required
  • Master's degree preferred

Minimum Experience

  • Two (2) years of direct experience in clinical biomedical and/or behavioral research required

Other Credentials

  • (LC: SOCRA or ACRP) Certification in clinical research from the Society of Clinical Research Associates (SoCRA) or the Association of Clinical Research Professionals (ACRP) must be obtained within three (3) years of assuming the position

What We Offer

WHATWE_Benefits          WHATWE_Glassdoor          WHATWE_UnexpectedPerks

 

 

WHATWE_Memphis

Other Information

St. Jude is an Equal Opportunity Employer

No Search Firms:

St. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.

COVID-19 vaccine:

St. Jude Children’s Research Hospital has mandated the COVID-19 vaccine for all employees, excluding those with an approved medical or religious accommodation, as a condition of employment.

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