Licensed Practical Nurse (Clinical Research)
at DelRicht Research
New Orleans, LA 70115, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 10 Nov, 2024 | USD 28 Hourly | 11 Aug, 2024 | 1 year(s) or above | Working Environment,Direct Patient Care,It,Data Collection,Clinical Trials,Clinical Research,Patient Care | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
WHY DELRICHT RESEARCH?
Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a position that has sustainable opportunity for professional growth? If the answer is yes, then DelRicht Research might be the right opportunity for you! We are a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new treatment options for our patients and, ultimately, our goal is to get new medications and medical devices FDA approved! We hold our team members to a high standard of excellence and are looking for energetic, positive, quick learners to be a part of our team.
WHO WE ARE
DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new treatment options for our patients and ultimately our goal is to get new medications and medical devices FDA approved! We hold our team members to a high standard of excellence and are looking for energetic, positive, quick learners to be a part of our team. Presently our network stretches across 33 sites throughout the United States in 18 states.
Please Note: This is an onsite M-F position based at our Uptown New Orleans clinic. No remote or hybrid seeking applicants please. Preference will be given to local candidates.
Clinical Research Coordinator’s Main Objective: Overall, our Clinical Research Coordinators are responsible for providing quality, excellent patient care and a great experience for our patients in our clinical research studies. Our coordinators maintain all activities related to the conduct of clinical trials at the site including but not limited to:
- Patients have a fun, positive and comfortable experience at our clinic
- Provide excellent care and a great experience for our patients in our clinical research studies
- Act as the unblinded resource in a double blind, double-placebo controlled study
- Be responsible for the constitution and administration of investigational products
- Accurately and efficiently conduct patient charting and review your own work for accuracy and quality
- General data collection for patient visits including patient questionnaires and entering data into multiple online systems
- Communicate effectively with the study team on charting and patient data
SKILLS NEEDED TO WIN:
- Required: LPN license
- Required: 1-2 years of professional experience in a Healthcare setting
- Required: Experience and comfort administering intramuscular (IM) injections
- Required: Experience with high touch documentation or independent patient charting
- Preferred: Comfortable working with minimal oversight
- Preferred: Experience with direct patient care
- Preferred: Pediatric healthcare experience
- Clinical research not required (but wonderful if you have it, of course!)
- A great, coachable attitude and a willingness to learn
- Enjoyment of a fast-paced working environment
- Coffee drinkers preferred. Tea drinkers accepted
Responsibilities:
- Patients have a fun, positive and comfortable experience at our clinic
- Provide excellent care and a great experience for our patients in our clinical research studies
- Act as the unblinded resource in a double blind, double-placebo controlled study
- Be responsible for the constitution and administration of investigational products
- Accurately and efficiently conduct patient charting and review your own work for accuracy and quality
- General data collection for patient visits including patient questionnaires and entering data into multiple online systems
- Communicate effectively with the study team on charting and patient dat
REQUIREMENT SUMMARY
Min:1.0Max:2.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Proficient
1
New Orleans, LA 70115, USA