Clinical Research Associate - San Diego, United States - Systems Ally

Systems Ally
Systems Ally
Verified Company
San Diego, United States

5 hours ago

Mark Lane

Posted by:

Mark Lane

beBee recruiter
Description

Comment:


Education:


  • Bachelors Degree or Higher

Top 3 skills you're looking for on resume:

  • on-site and remote monitoring experience 2-5 years.
- experience with study start up, monitoring, and close out activities
- ability to work independently, get training done and able to hit the ground quickly.

  • Monitor and maintain necessary supplies, with approval by senior department staff.
  • Support and/or lead clinical research study start up activities (includes creation of study binders, study logs, work instructions, case report form, and other study related materials)
  • Ability to train site personnel on study activities including investigational product usage, maintenance and accountability, sample collection, testing and shipping, data entry and query resolution.
  • Study monitoring (includes assessing the familiarity of the site personnel with the protocol, procedures, and investigational product, assessing protocol compliance and investigational product accountability as applicable, source document verification, identifying protocol deviations, writing queries, writing monitoring reports, notes to file, and other documentation as necessary)

RESPONSIBILITIES:


  • Monitor and maintain necessary supplies, with approval by senior department staff.
  • Support and/or lead clinical research study start up activities (includes creation of study binders, study logs, work instructions, case report form, and other study related materials)
  • Ability to train site personnel on study activities including investigational product usage, maintenance and accountability, sample collection, testing and shipping, data entry and query resolution
  • Study monitoring (includes assessing the familiarity of the site personnel with the protocol, procedures and investigational product, assessing protocol compliance and investigational product accountability as applicable, source document verification, identifying protocol deviations, writing queries, writing monitoring reports, notes to file, and other documentation as necessary)
  • Independent site management skills to assist with study problem identification and solving, and ensure timely study progression
  • Understanding of clinical research activities including tasks associated with study start up, interim monitoring, close out, data collection and central files
  • Team player able to deliver on project timelines.
  • Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices; build productive internal/external working relationships
  • Other duties as assigned, according to the changing needs of the business.

Job Type:
Contract


Pay:
$ $35.00 per hour


Benefits:


  • 401(k)
  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance

Experience level:

  • 3 years
  • 4 years

Schedule:

  • 8 hour shift
  • Day shift
  • Monday to Friday

Education:


  • Bachelor's (preferred)

Experience:


  • Clinical research associate: 4 years (preferred)
- on-site and remote monitoring: 4 years (preferred)
- study start up, monitoring, and close out activities: 4 years (preferred)
- pharma or medical device industry: 3 years (preferred)


Ability to Commute:

  • San Diego, CA required)

Work Location:
In person
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