Responsibilities:
- Coordinate and oversee clinical research studies from start to finish
- Ensure compliance with regulatory requirements, including HIPAA,IRB and 1572 submissions.
- Review and maintain documentation for each study participant
- Knowledge of good clinical practice (GCP) guidelines and regulations governing clinical research.
- Collect and document data accurately and in compliance with protocols
- Assist in the preparation of reports and presentations for clinical trials
-Go over study protocol, requirements, staff training, site qualification, etc
Requirements:
- Previous experience in clinical research coordination preferred at least 2 years minimun
- Strong knowledge of clinical research processes and protocols
- Strong communication and interpersonal skills in english and spanish
- Familiarity with statistical software and systems used in clinical trials
- Excellent organizational skills and attention to detail
- Ability to work independently and as part of a team
-May communicate with study participants to answer questions and provide updates, as well as with other stakeholders such as study sponsors, principal investigators, and regulatory agencies.
Note: This job description is intended to provide a general overview of the position. Other duties may be assigned as necessary to support the goals of the organization.
Job Types: Full-time, Part-time
Pay: $25.00 - $35.00 per hour
Expected hours: 40 per week
Schedule:
Application Question(s):
- business development, Billing, budget and contracts
Education:
- High school or equivalent (Preferred)
Experience:
- business development, Billing, budget and contracts: 4 years (Preferred)
- Business development, budget and contracts: 4 years (Required)
Language:
- english and spanish (Required)
Work Location: In person
