Clinical Research Study Assistant I - Orthopedic Surgery
at Washington University in St Louis
Creve Coeur, MO 63141, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 01 Feb, 2025 | USD 25 Hourly | 01 Nov, 2024 | 1 year(s) or above | Interpersonal Communication,Customer Service,Information Organization | 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:
POSITION SUMMARY
Performs a variety of research, database and clerical duties of a routine and technical nature in support of clinical research to ensure adherence to protocols and quality of information received.
EDUCATION:
High school diploma or equivalent high school certification.
WORK EXPERIENCE:
Customer Service (1 Year)
SKILLS:
Not Applicable
EDUCATION:
No additional education beyond what is stated in the Required Qualifications section.
WORK EXPERIENCE:
Medical Customer Service (1 Year)
SKILLS:
Detail-Oriented, Information Organization, Interpersonal Communication
Responsibilities:
- Maintains and updates site demographics on computer database; logs forms received and files as appropriate; prepares reports from database to include weekly reports and other reports as requested.
- Receives and disseminates study-related regulatory documents and correspondence; assists in screening documents for completeness and compliance with protocol and appropriate regulations; assists in investigating incomplete, inaccurate or missing documents to ensure accuracy and completeness of data.
- Communicates and coordinates with other study personnel as required to include data entry and randomization of personnel, pharmacy, laboratories, study sponsors and others as needed for study implementation and routine problem resolution.
- Attends routine meetings and other meetings related to the clinical research; stays abreast of information and any changes to study protocol.
REQUIREMENT SUMMARY
Min:1.0Max:6.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Diploma
Proficient
1
Creve Coeur, MO 63141, USA