PART TIME Clinical Research Coordinator I
$52,243–$52,243 year
On-siteNewport News, Virginia, United States
Job Summary
Conduct high quality clinical research following ethical and regulatory standards by reviewing study protocols, assessing subject eligibility, and enrolling patients with informed consent. Organize sites for equipment and supplies, order and dispense medications, and process lab specimens including blood and urine. Collect and maintain study data, prepare case report forms and adverse event reports, and monitor compliance with federal regulations and sponsor audits. Schedule subject appointments, track enrollment status, and collaborate with investigators to prepare study reports. Maintain contact with sponsors to coordinate site visits and answer data-related questions.
Required Qualifications
- Bachelor's degree from a four-year college or university
- One to two years related experience and/or training
- Equivalent combination of education and experience
- Legible handwriting
- Current driver's license
- Reliable vehicle
- Ability to stand and walk for long periods of time
- Ability to sit for extended periods of time
- Ability to climb or balance for limited periods of time
- Ability to occasionally reach, bend, stoop and lift up to 50 lbs
- Ability to grasp and hold up to 25 lbs
- Ability to hear normal voice level communications in person or through the telephone
- Ability to speak clearly and understandably
- Ability to taste and smell
- Ability to look at a computer screen for many hours of the day
- Ability to work scheduled hours as defined in the job offer and to use time effectively
- Ability to determine appropriate course of action in more complex situations
- Ability to present information to top management, public groups, and/or boards of directors effectively
- Ability to define problems, collect data, establish facts, and draw valid conclusions
- Ability to manage multiple and simultaneous responsibilities
- Ability to read and understand oral and written instructions and follow written protocols
- Ability to manage data, prepare spread sheets, and apply mathematical concepts such as probability, statistical inference, and basic concepts of algebra and geometry to practical situations
- Knowledge of appropriate medical terminology
- Knowledge of appropriate email etiquette and effective communication
- Knowledge of clinical study affairs and issues
- Ability to work well independently and with a team
- Ability to refocus attention easily after multiple interruptions
- Ability to remain organized despite multiple paper charts being utilized at the same time
- Willing to perform work related tasks off-site when necessary
- Willing and eager to learn new things
- Monday through Thursday schedule
- Either 7:00 AM–1:00 PM or 8:00 AM–2:00 PM schedule
Desired Qualifications
- Patient care experience
- Phlebotomy experience
- GCP certification
- IATA certification
- Certification by the Association of Clinical Research Professionals (ACRP) or similar organization
- Ability to learn new tasks and apply skills and knowledge to various work activities
- Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical study affairs and issues
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