Clinical Research Coordinator

4 days ago

Los Angeles, United States Ultimate Staffing Full time
In Office: 90036

Job Type: Full-time M-F 8-5

Pay: $30.00 - $40.00 per hour

Expected Hours: 40 hours per week.
Dress code: Business Professional

In Office or Remote: Onsite

Parking details: Provided
Start Date/ Interview Schedule: ASAP

Position Summary:
The Clinical Research Coordinator (CRC) is responsible for coordinating and administering clinical trials under the guidance of the Medical Director. This role involves developing, implementing, and managing research and administrative procedures to ensure the successful execution of clinical trials. The CRC must perform diverse administrative duties, requiring sound judgment, analytical skills, and in-depth knowledge of study-specific protocols.

Key Qualifications & Requirements:

  • Strong ability to read, analyze, and interpret professional journals, technical procedures, and governmental regulations.
  • Effective verbal and written communication skills; able to present information and respond to questions from physicians, staff, and patients.
  • Minimum of five (5) years of clinical research experience required.
Primary Duties and Responsibilities:
  • Coordinate and manage 5-10 clinical trials, adhering to Research Standard Operating Procedures (SOPs), Good Clinical Practices (GCP), and study protocols
Desired Skills and Experience

In Office: 90036
Job Type: Full-time M-F 8-5
Pay: $30.00 - $40.00 per hour

Expected Hours: 40 hours per week.
Dress code: Business Professional
In Office or Remote: Onsite

Parking details: Provided
Start Date/ Interview Schedule: ASAP
Position Summary:
The Clinical Research Coordinator (CRC) is responsible for coordinating and administering clinical trials under the guidance of the Medical Director. This role involves developing, implementing, and managing research and administrative procedures to ensure the successful execution of clinical trials. The CRC must perform diverse administrative duties, requiring sound judgment, analytical skills, and in-depth knowledge of study-specific protocols.
Key Qualifications & Requirements:
Strong ability to read, analyze, and interpret professional journals, technical procedures, and governmental regulations.
Effective verbal and written communication skills; able to present information and respond to questions from physicians, staff, and patients.
Minimum of five (5) years of clinical research experience required.
Primary Duties and Responsibilities:
Coordinate and manage 5-10 clinical trials, adhering to Research Standard Operating Procedures (SOPs), Good Clinical Practices (GCP), and study protocols

All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

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