CLINICAL CORRELATION COORDINATOR I
3 weeks ago
Shift Day Employee type Regular Full-Time Work mode On-site
Clinical Correlation Coordinator I - San Juan Capistrano, CA - Monday to Friday 8:00AM-5:00PM
Responsible for performing daily phlebotomy activities, clinical specimen identification, and clinical specimen processing following established standard operating procedures in support of ongoing operational testing as well as new assay development. Activities may be focused individual projects or assignments as a member of a project team.
Pay Range: $21.38 - $32.08 / hour
Salary offers are based on a wide range of factors including relevant skills, training, experience, education, and where applicable, certifications obtained. Market and organizational factors are also considered. Successful candidates may be eligible to receive annual performance bonus compensation.
Benefits Information:
We are proud to offer best-in-class benefits and programs to support employees and their families in living healthy, happy lives. Our pay and benefit plans have been designed to promote employee health in all respects - physical, financial, and developmental. Depending on whether it is a part-time or full-time position, some of the benefits offered may include:
* Day 1 Medical/Dental/Vision for FT employees who work 30+ hours
* 15 PTO days first year
* Paid Holidays
* Annual Bonus Opportunity
* 401(k) with matching contributions
* Variable compensation plan (AIP) bonus
* Employee Stock Purchase Plan (ESPP)
* Employee Assistance Program (EAP)
* Blueprint for Wellness
* Tuition Reimbursement for undergraduate and graduate programs for FT employees who work 30+ hours
* Opportunities for career advancement
* Training provided
* Coordinate the acquisition, receipt, inventory, identification, distribution, retention, and destruction of clinical specimen used in assay development.
* Coordinate the acquisition, receipt, and distribution of research results for statistical analysis as needed.
* Understands specimen collection protocols (i.e. blood cultures, chain-of-custody, mid-stream urine collection).
* Demonstrates appropriate phlebotomy skill for level of experience (i.e. 95% success rate on first venipuncture per patient).
* Participate in the planning and implementation of internal/external blood draw events.
* Administer National Quality Assurance blind studies to monitor assay performance.
* Support Quality Assurance Internal Proficiency Testing programs.
* Administer phlebotomy training in collaboration with CLS Training Programs Manager
* Maintain the proper characterization, documentation, and storage of specimen using the Clinical Studies Integrated Systems biobank management application.
* Supports compliance for HIPAA regulations and company policies. Ensures compliance with all regulatory agency requirements through documentation audits or corrective actions.
* Understands and abides by Universal Precautions procedures.
* Ability to communicate in a professional manner with donors and outside vendors.
* Maintains good public relation skills.
* Perform other duties as assigned.
QUALIFICATIONS
Required Work Experience:
* Minimum of 2 years of phlebotomy experience
* Minimum of 2 years of general laboratory experience
Preferred Work Experience:
N/A
Physical and Mental Requirements:
Must be flexible and available based on staffing requirements (weekends, holidays, on call, and/or overtime)
Knowledge:
N/A
Skills:
* Demonstrated proficiency in computer skills such as word processing, statistical analysis, and laboratory information systems.
* Strong interpersonal skills and communication skills.
EDUCATION
High School Diploma or Equivalent(Required)
LICENSECERTIFICATIONS
Phlebotomy Technician Certification (CPT)(Required)
Quest Diagnostics honors our service members and encourages veterans to apply.
While we appreciate and value our staffing partners, we do not accept unsolicited resumes from agencies. Quest will not be responsible for paying agency fees for any individual as to whom an agency has sent an unsolicited resume.
2024-60550
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