Clinical Research Assistant I - Surgery
at Mount Sinai
New York, NY 10029, USA -
| Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
|---|---|---|---|---|---|---|---|
| Immediate | 23 Jan, 2025 | USD 25 Hourly | 24 Oct, 2024 | 1 year(s) or above | Research,Role Model,Medicine,Patient Care,Discrimination | 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:
Description
The Clinical Research Assistant I assists in the daily activities of clinical research studies, including collection and organization of study information. Assists in preparing grant applications and documents (e.g., Institutional Review Board, Grants and Contracts Office), and provides clerical support to Clinical Research Coordinators and others in assigned area.
Responsibilities
- Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
- Collects and records study data. Inputs all information into database.
- Assists in preparing grant applications, IRB/GCO for submission and filings.
- Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.
- Secures, delivers and ships clinical specimens as required by the protocol.
- Assists in the preparation for monitoring visits.
- Performs other related duties.
QUALIFICATIONS
- Associates Degree in Science or closely related field preferred or HS/GED plus two years of related experience
- 1 year in research environment preferred
Non-Bargaining Unit, 862 - Surgery - ISM, Icahn School of Medicine
Employer Description
Responsibilities:
- Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
- Collects and records study data. Inputs all information into database.
- Assists in preparing grant applications, IRB/GCO for submission and filings.
- Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.
- Secures, delivers and ships clinical specimens as required by the protocol.
- Assists in the preparation for monitoring visits.
- Performs other related duties
REQUIREMENT SUMMARY
Min:1.0Max:2.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Proficient
1
New York, NY 10029, USA
