• Employment type: Direct Hire (Permanent)
  

• Location: Inglewood CA (On-site)
  

• Salary Range: $70 to $75 w-2 hourly (145k – 156k salary range)

Kelly® Science & Clinical is hiring a Clinical Research Sub-Investigator for a direct-hire opportunity with one of our growing clinical research clients. If you’re passionate about advancing scientific discovery and ready to elevate your career, trust The Experts at Hiring Experts.

SUMMARY: The Sub-Investigator is a member of the clinical research trial team who supports the Principal Investigator in identifying eligible research patients, performing medical assessments and the medical decisions needed for their treatment. The Sub-Investigator is under the guidance and direct supervision of the site Principal Investigator MD.

ESSENTIAL DUTIES AND RESPONSIBILITIES: include the following. Other duties may be assigned.

• Comply with all company policies, procedures, and conduct.
  

• Strictly adhere to confidentiality and compliance standards.
  

• Review medical histories and concomitant medications of study subjects.
  

• Confirm inclusion and exclusion study criteria.
  

• Field subject questions related to the investigational product, study procedures and health.
  

• Provide medical oversight required for medically attended events such as vaccinations and infusions.
  

• Maintain GCP and study specific training requirements.
  

• Oversee aspects of clinical trials as directed by the site Investigator MD.
  

• Perform clinical study-related procedures.
  

• Make medical judgements and other decisions on behalf of the Investigator MD.
  

• Meet all study protocol requirements and deadlines.
  

• Perform accurate and timely documentation in eSource.
  

• Assist in answering queries and documentation in eSource.
  

• Work closely with CRO/CRA/IRB. 
  

• Other tasks as assigned.

QUALIFICATIONS:

• Advanced degree as an MD, PA-C or Nurse Practitioner, required.
  

• Active and unrestricted license in the state of practice, required.
  

• Prior experience in pharmaceutical research, clinical trials or academia is highly desirable.
  

• Proficiency in research methodologies, data analysis software and statistical tools.
  

• Strong analytical and critical thinking skills for research design and data interpretation.
  

• Excellent written and verbal communication skills.
  

• Experience preparing research reports and presentation of findings.
  

• Thorough understanding of research regulations, guidelines, and standards (i.e., FDA, ICH, GCP).
  

• Flexibility to adapt to evolving research priorities and changing project requirements.
  

• A proven ability to multi-task in a rapidly changing environment.

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