Sr. Clinical Research Specialist

Kelly Science, Engineering, Technology & Telecom

Irvine (CA)

Hybrid

USD 110,000 - 160,000

Full time

14 days+
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Job summary

Kelly FSP Group in Irvine, CA is seeking a Sr. Clinical Research Specialist (Sr. CRS) to oversee feasibility, site selection, setup, conduct and closure of clinical trials in a hybrid work model.

You will coordinate device accountability, support physicians and cross-functional teams, and help develop essential trial documents while ensuring regulatory and quality standards.

Qualifications

  • Oversee feasibility and site selection for clinical trials.
  • Assist in development of study documents (protocols, informed consent, CRFs).
  • Ensure registration on ClinicalTrials.gov and support publications as needed.

Responsibilities

  • Oversee feasibility, selection, setup, conduct and closure of clinical trials.
  • Manage device accountability, case support and daily interactions with physicians and cross-functional team members.

Job description

The Kelly FSP group is currently hiring for a Sr. Clinical Research Specialist (Sr. CRS) who will be hybrid out of an Irvine, CA based sponsor location.

The Sr. CRS is responsible for oversight/execution of feasibility, selection, set up, conduct and closure of clinical trials. These site facing roles will also focus on device accountability, case support and daily interactions with physicians as well as other cross functional team members.

Additional responsibilities may include:

  • May serve as the primary contact for clinical trial sites (e.g. site management)
  • Contribute towards development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports), ensure registration on www.clinicaltrials.gov from study initiation through posting of results and support publications as needed
  • Management/oversight of ordering, tracking, and accountability of investigational products and trial materials
  • Oversee the development and execution of Investigator agreements and trial payments
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