Clinical Research Coordinator
- Compensation
- $30–$33 / hr
- Location
- Northridge, California, United States
- Work setup
- Not specified
- Seniority
- Not specified
- Employment
- Not specified
- Experience
- 3+ years
- Category
- Healthcare
- Posted
Skills
Must have
- PHYSICAL REQUIREMENTS AND/OR ENVIRONMENTAL FACTORS:
- A. Work is normally performed in a typical interior/office work environment.
- B. Travel required.
- C. Exposure to human bodily fluids.
- D. Laboratory processing procedures.
- E. Subject/Patient care.
- F. Daily computer use.
- G. Occasional night and weekend work schedules.
- H. The ability to properly lift thirty-five pounds and occasionally more than thirty-five pounds.
- I. The ability to drive, and daily availability of an automobile.
- MINIMUM REQUIREMENTS:
- Education: Bachelor's degree preferred; however, is not required.
- Experience: Preferably a minimum of 2 years’ experience as a CRC, plus 1-3+ years' minimum experience
- within the field of clinical research or biological research.
- Knowledge and Skills:
- A. Exceptional knowledge of clinical research methods.
- B. Strong management and leadership skills.
- C. Demonstrated ability to collaborate and align with operations.
- D. Excellent oral and written communication skills.
- E. Excellent computer skills to include Office365 products.
- F. Experience in writing and reviewing Standard Operating Procedures.
- G. Strong problem solving, risk assessment and impact analysis abilities.
- H. Demonstrated experience in process improvement.
- I. Strong negotiation and conflict management skills.
- able to multi-task and prioritize competing demands.
- K. Ability to think independently and influence when appropriate
Full description
About Us:
Flourish Research is where clinical trials thrive. Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
About the Job:
We are actively hiring a Clinical Research Coordinator to support our Northridge, California site.
Shift: Monday-Friday day shift (40 hours per week)
Location: Onsite, Northridge, CA
FLSA Classification: Non-Exempt
Compensation: $30 to $33 per hour (depending on experience)
ESSENTIAL JOB FUNCTIONS:
A. Read, understand, and can accomplish protocol specified patient visits and procedures.
B. Clearly and concisely document patient assessments, observations, test results and other study related
information per federal regulations, protocol requirements and GCPs.
C. Obtain patient informed consent according to federal regulations, GCPs and IRB requirements.
D. Is creative and diligent in recruiting qualified study subjects into assigned protocols to fulfill enrollment
obligations within the sponsor’s timeline while following regulations and rules governing medical
ethics, IRB, GCP and ICH guidelines.
E. Complete all required training in a timely manner.
F. Schedule and conduct patient visits according to protocol requirements and timelines.
G. Maintain accurate and complete written source documentation of patient visits and protocol related