Clinical Trial Coordinator (Remote)
at Cognizant
Michigan, Michigan, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 17 Sep, 2024 | USD 24 Hourly | 18 Jun, 2024 | N/A | G Suite,Salesforce,Soft Skills,Communication Skills,Time Management,English,Regulatory Requirements | 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:
Cognizant (NASDAQ: CTSH) is a leading provider IT and BPO services, providing critical initiatives to a variety of global clients. Clinical Trial Coordinator provides rigorous clinical study support to client’s study participants. The primary role of the Clinical Trial Coordinator is to support study participants in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs).
MINIMUM QUALIFICATIONS
- Education: Healthcare BS/BA degree or equivalent experience
- Fluent in English with excellent written and verbal communication skills
- Experience supporting clinical study operations and interacting with study participants
- Empathetic and tech savvy, with strong attention to detail
- Confident presenter with solid soft skills on the phone
PREFERRED QUALIFICATIONS
- Knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP)
- Proficiency with G Suite and Salesforce
- Effective time management and organizational skills
- Attention to detail and accuracy in work
ABOUT US:
Cognizant (Nasdaq-100: CTSH) is one of the world’s leading professional services companies, helping organizations modernize technology, reimagine processes and transform experiences so they stay ahead in a fast-changing world.
Responsibilities:
- Study participant support over phone and email through inbound and outbound activity (calls and emails)
- Participant enrollment and consent verification, as needed
- Technical troubleshooting for devices, application, and other study tools/resources
- Gather feedback from participants
- Other duties, as assigned
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Proficient
1
Michigan, USA