Job Description
Our Client, a Healthcare company, is looking for a Clinical Research Coordinator - Hybrid job for their Orange, CA location.
Responsibilities:
Requirements:
Why Should You Apply?Excellent growth and advancement opportunities
#mcb
Responsibilities:
- Reads and understands all correspondence relating to each study assigned. Responsible for all written and verbal communication and the documentation thereof. This will include but not be limited to communications with study sponsors, monitors, study subjects/patients, physicians and laboratories or other study-specified service providers.
- Responsible for all IP accountability specific to each subject and total protocol inventory. Role includes proper documentation of IP assignment, temperature and expiration date monitoring, return of used IP, and destruction or return to sponsor.
- Works with subjects/patients to ensure study compliance and understanding of participation requirements (i.e., timeliness of visits, return of study-related materials and at-home documentation.
- Complete, accurate and timely entry (within 7 days of visit) of visit data into study electronic data capture sites when applicable.
- Recruits and retains study Participants.
- Processes, packages, and ships biological samples as required by study or centralized laboratories.
- Organizes and maintains study binders for each participant in a study. Ensures that filing is complete, accurate and consistent among study participants.
- Attends investigators’ meetings as required.
- Works with patients to ensure that study requirements are met including appointments, labs, etc.
- Networks and researches potential new studies.
- Performs regulatory functions for existing studies.
- Maintains control over study medications/supplies.
Requirements:
- Prefer to have a minimum of two years of experience in a Clinical Research setting where coordinator managed patients.
- Cardiology/Stroke specialty a plus.
- Device trial experience will not be accepted. Solely data trials experience also not accepted.
- Minimum 2 years experience in a clinical research setting where candidate managed patients (consent them, perform vitals/EKG, process labs, dispense medication, complete documentation, enter data)
- Must Have Epic Experience
- Must also have strong computer skills - Outlook, MS Teams, Word, Excel
Why Should You Apply?Excellent growth and advancement opportunities
#mcb
Numbers & Facts
| Location | Orange, CA |
| Industry | Management Consulting Services |
| Salary | $40–$42 Per Hour |
| Company Size | 2,000 to 2,499 employees |
| Year Founded | 2000 |
| Website | https://www.iconma.com/ |
Benefits
401K, Employee Referral Program, Life Insurance
About Company
ICONMA is a global information consulting management firm providing Professional Staffing Services and Project-Based Solutions for organizations in a broad range of industries.
- Corporate Headquarters in Troy, Michigan; 20+ locations worldwide.
- Certified Woman-Owned Business Enterprise (WBE); certified by Women’s Business Enterprise National Council, National Women Business Owners Corporation (NWBOC); and California Public Utilities Commission (CPUC).
- Founded in 2000
- 2000+ Employees
The company was founded on the principle that success is derived from delivering high quality service and resources in the most responsive, flexible, and innovative way. ICONMA invests in people and resources with a single goal: To provide our customers with the highest quality service in the most responsive manner. Through its network of offices, ICONMA provides the resources to help clients maintain their competitive advantage.
Skills
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