Clinical Research Associate I (SC4) job Oro Valley Arizona
Clinical Research Associate I (SC4) job Oro Valley Arizona
My Spider Scam Awareness Contacting Us F. A. Q.
 
Job Seekers
Search Jobs
Browse Jobs
Post a Resume
Job Alerts
 
Employers
Search Resumes
Browse Resumes
Post a Job

Clinical Research Associate I (SC4) Job



Employer Name: SpiderID: 8408667
Location: Oro Valley, Arizona Date Posted: 2/12/2019
Wage: Up to $0.00 per year Category: Science/Research
Job Code: 51263

Job Description:


Clinical Research Associate I. We have a contract need in Tucson, AZ for a local Clinical Research Associate I who will be involved in all aspects of developing, implementing and closing Design Control Studies including verification and validation studies, and Clinical Studies conducted by Clinical Affairs involving instruments, software and reagents used in tissue-on-slide based in-vitro diagnostic tests.

Position Accountabilities:



  • Assist withpre-study coordination and determination of readiness including record keeping for the following activities:

    • Study site management

    • Initiate Interactions with investigators and their staff on behalf of the client.

    • Protocol and Case Report Form Development.

    • Study supplies management.

    • Training investigators and their study team.



  • In-house or on-site monitoring of studies including record keeping; May be required to travel intermittently up to 30%.

  • Database development and management including record keeping for the following activities:

    • Validation

    • Data entry

    • Data verification

    • Clarifications

    • Corrections

    • Preparation for analysis



  • Study report reviews, writing, and compilation including record keeping.

  • Participate on cross functional study teams.

  • Monitor work to ensure quality, and continuously promote Quality First Time.




Position Requirements:



  • Bachelor of Science OR equivalent combination of education and experience.

  • 2+ years of previous pharmaceutical or medical device clinical study coordination or clinical study management experience required.

  • Computer literate (Word, Excel, Access, PowerPoint).

  • Excellent writing skills.

  • Excellent phone skills.

  • Well organized and detail oriented.

  • Impeccable record keeping and filing skills.

  • Excellent time management skills.

  • Ability to make presentations well, and teach.

  • Excellent communicator.

  • Previous experience with FDA/ICH/GCP

  • Self motivating and a team player.

  • Proficient at managing multiple priorities and tasks.




Preferred Qualifications:



  • Knowledge of current Good Clinical Practices (cGCP) and Code of Federal Regulations (CFR) preferred.

  • A background in molecular biology/biochemistry with laboratory experience preferred.

  • Would prefer at least 1-2 years prior research experience, in drug or device research.




To view all our open positions, please go to: http://www.jobs.net/jobs/fastswitch/en-us/all-jobs/



Job Criteria:
Start Date: 03/04/2019
Position Type: Contractor
Years of Experience Required:
Education Required:
Overnight Travel:
Vacation Time:


Contact Information:
Contact Name: Fast Switch LTD Company Type:
Company: Fast Switch LTD
City:
State:
Zip:

Send ad to a friend
Report a Problem


    





© 2019 Job Spider
Privacy Policy | CC Marketing Sites | Site Map | Links