Clinical Data Coordinator

Collabera; Los Angeles (CA); On-site; USD 27,552 - 34,440; Part time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) retirement plan

Life insurance

Short-term disability insurance

Paid vacation time

Paid parental leave

Paid holidays

Job summary

A leading staffing firm in Los Angeles is seeking a Clinical Data Coordinator to ensure the accuracy and integrity of clinical trial data. The ideal candidate will have a bachelor's degree in life sciences, strong organizational skills, and proficiency in MS Office. This role offers competitive pay and an excellent benefits package including medical, dental, and vision insurance.

Qualifications

• Bachelor's degree in life sciences or related field required.
• Strong data management, organizational, and communication skills needed.
• Excellent attention to detail and proficiency with MS Office applications.

Responsibilities

• Enter, review, and update clinical data per approved guidelines.
• Manage Data Clarification Forms (DCFs) and maintain organized study files.
• Support data validation, query resolution, and database lock activities.
• Ensure all processes comply with SOPs and regulatory standards.

Skills

Data management

Organizational skills

Communication skills

Attention to detail

Proficient with MS Office

Education

Bachelor’s degree in life sciences or related field

Tools

EDC systems

Job description

Join to apply for the Clinical Data Coordinator role at Collabera

This range is provided by Collabera. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$20.00/hr - $25.00/hr

Direct message the job poster from Collabera

Clinical Data Coordinator (CDC) role based in Sylmar, CA (Onsite)

Description:

• The Clinical Data Coordinator ensures the accuracy and integrity of clinical trial data across electronic and paper-based studies. Working under general supervision, the CDC supports multiple studies and collaborates with clinical teams to maintain compliance with Good Clinical Data Management Practices (GCDMP).

Responsibilities:

• Enter, review, and update clinical data per approved guidelines.
• Manage Data Clarification Forms (DCFs) and maintain organized study files.
• Support data validation, query resolution, and database lock activities.
• Ensure all processes comply with SOPs and regulatory standards.

Required Skills:

• Bachelor’s degree in life sciences or related field.
• Strong data management, organizational, and communication skills.
• Excellent attention to detail.
• Proficient with MS Office applications.

Preferred Skills:

• Experience with EDC systems and clinical data processes.
• Familiarity with GCDMP and clinical research documentation practices.

Pay range:

$20/hr. - $25/hr.

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable)

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Engineering and Information Technology