Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
DL
Diagnostic Laboratory Services, Inc.
Clinical Research Associate - Clinical Research Admin (Temporary Full Time, 40, Day)
Career Insights for Clinical Research Associate
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Hawaii data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Clinical Research Associate is responsible for running clinical trials, usually for an organization undertaking pharmacological drug testing. Will ensure that trials adhere to good clinical practice guidelines for monitoring clinical trials.
$106,078 / year median in Hawaii
-3% projected decline
Job Description
Responsibilities Review Date:
04/25Effective Date:
07/21 I.JOB SUMMARY/RESPONSIBILITIES
- Conducts clinical research studies under the immediate direction of assigned Principal Investigator.
- Assists researchers, clinical and administrative personnel in performing a variety of duties on a research project.
II. TYPICAL PHYSICAL DEMANDS
Essential:
standing, sitting, walking, seeing, hearing, speaking static gripping of an object for prolonged periods, frequent gripping of an object.Frequent:
lifting and carrying usual weight of 2 pounds up to 10 pounds, repetitive arm/hand motions.Occasional:
walking on uneven ground, finger dexterity, reaching above, at and below shoulder level.- Operates computer, printer, copier, telephone, calculator, facsimile.
III. TYPICAL WORKING CONDITIONS
- Not substantially subjected to adverse environmental conditions.
- Must be flexible to accommodate the nature of research (early morning sample collection/preparation).
- May need to work some nights and weekends.
IV. MINIMUM QUALIFICATIONS
A.EDUCATION/CERTIFICATION AND LICENSURE
- Bachelor's degree in science or related field.
- Current certification in
BLS/HCP. B. EXPERIENCE
- Minimum two (2) years experience working in a research setting.
- Experience to demonstrate knowledge of research regulatory processes (human subject protection, biological safety, conflict of interest, research misconduct), guidelines, rules and regulations and policies and procedures.
- Advanced skills in the use of relational databases (e.