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Hybrid Prescreen Coordinator I bei None

None · San Diego, Vereinigte Staaten Von Amerika · Hybrid

39.520,00 $  -  45.760,00 $

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SUMMARY: The Pre-Screening Coordinator is responsible for coordinating and overseeing site screening schedules, managing pre-screening operations and overseeing patient eligibility assessments. If you are a motivated professional with a passion for clinical research and patient engagement, we invite you to apply!  

 

ESSENTIAL DUTIES AND RESPONSIBILITIES: 

  • Review and breakdown protocols and informed consents for patient eligibility and recruitment. 
  • Conduct prescreen visits and assessments. 
  • Must have excellent organizational, attention to detail, interpersonal skills, and possess a high level of multi-tasking capacities.
  • Maintain a thorough understanding of various research study guidelines that include both inclusion and exclusion criteria. 
  • Explain the study procedures and answer questions to ensure that potential participants understand the study requirements and process.
  • Explain the study’s purpose, procedures, risks, benefits, compensation and follow up care to potential participants prior to entry into the study.
  • Perform screening exams on participants to determine their health status prior to participating in studies involving new medications or procedures. 
  • Create and maintain detailed records of all call logs and study candidates including their names, addresses, phone numbers, birth dates and other identifying information. 
  • Collect and analyze test results from candidates to determine if they have any physical impairments that could interfere with their participation in the study.
  • Oversee site screening schedules, ensuring all activities adhere to compliance requirements. 
  • Coordinate performance and time efficiency in the prescreen visit flow. 
  • Comply with all company policies, procedures, and conduct.
  • Strictly adhere to confidentiality and compliance standards.

 

QUALIFICATION REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. 

EDUCATION AND EXPREIENCE:  

  • Associate’s degree in healthcare or related field, preferred.
  • Certified Phlebotomy Technician (CPT) license required. 
  • Certified Medical Assistant or related field, preferred.
  • 2 years’ experience in running research protocols, preferred. 
  • 2 years’ experience in FDA regulations and GCP, preferred. 
  • Proven track record of analytic reasoning skills and problem solving.
  • Exceptional attention to details and organization.
  • Must possess excellent verbal and written communication skills.
  • A proven ability to multi-task in a rapidly changing environment.


Jetzt bewerben

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