Research Assistant
at Columbia University
New York, New York, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 28 Aug, 2024 | USD 58102 Annual | 29 May, 2024 | 5 year(s) or above | Training,Spanish | 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:
- Job Type: Support Staff - Union
- Bargaining Unit: SSA
- Regular/Temporary: Regular
- End Date if Temporary:
- Hours Per Week: 35
- Standard Work Schedule:
- Building:
- Salary Range: $58,102.42 - $58,102.42 annually
The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training. The above hiring range represents the University’s good faith and reasonable estimate of the range of possible compensation at the time of posting.
Position Summary
The Research Assistant will assist in the data collection for observational Lewy body disorders (Parkinson’s disease dementia, Parkinson’s disease) and Huntington’s disease studies and investigator-initiated trials, with particular focus on Parkinson’s disease and Deep Brain Stimulation (DBS).
Responsibilities
Responsibilities involving recruitment, questionnaires, neuropsychological testing, data entry and biofluid handling. The Research Assistant will work under the supervision of the Senior Research Managers and the study Principal Investigators.
The position involves roles and responsibilities that include, but are not limited to:
- Screen charts, recruit, schedule, and consent subjects for studies.
- Prepare for upcoming study visits.
- Conduct clinical interviews with study participants and use study-specific assessments, physical examination assessments, review of medical history, cognitive and neuropsychological testing, and other questionnaires.
- Process blood and other biological samples such as cerebrospinal fluid (CSF) and urine as per study procedures.
- Accurately collect and enter data into databases and electronic case report forms.
- Adherence to federal and institutional regulations and GCP guidelines.
- Assist with other administrative and research activities as required.
- Assist in the maintenance, programming, and management equipment used to collect data such as laptops, tablets, and devices distributed to participants for passive monitoring of movements and activities such as smartphones and smartwatches provided by the study.
- Perform other related duties and responsibilities as assigned/requested.
Responsibilities:
- Screen charts, recruit, schedule, and consent subjects for studies.
- Prepare for upcoming study visits.
- Conduct clinical interviews with study participants and use study-specific assessments, physical examination assessments, review of medical history, cognitive and neuropsychological testing, and other questionnaires.
- Process blood and other biological samples such as cerebrospinal fluid (CSF) and urine as per study procedures.
- Accurately collect and enter data into databases and electronic case report forms.
- Adherence to federal and institutional regulations and GCP guidelines.
- Assist with other administrative and research activities as required.
- Assist in the maintenance, programming, and management equipment used to collect data such as laptops, tablets, and devices distributed to participants for passive monitoring of movements and activities such as smartphones and smartwatches provided by the study.
- Perform other related duties and responsibilities as assigned/requested
REQUIREMENT SUMMARY
Min:5.0Max:10.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Education training and experience
Proficient
1
New York, NY, USA