Associate Clinical Data Manager at Katalyst Healthcares Life Sciences
Irvine, California, USA -
Full Time


Start Date

Immediate

Expiry Date

08 Oct, 25

Salary

0.0

Posted On

09 Jul, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Excel, Life Science, Software, Public Health, Powerpoint, Management Skills, Technical Systems, Communication Skills

Industry

Pharmaceuticals

Description

COMPANY DESCRIPTION

  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
    Job Description

JOB DESCRIPTION:

We are seeking a motivated and detail-oriented Associate Clinical Data Manager to join our Clinical Data Management (CDM) team. This is an entry-level position ideal for candidates looking to start a long-term career in clinical research and data management. In this role, you will assist with the oversight and coordination of data collection, cleaning, and quality review activities for clinical trials.

REQUIREMENTS:

  • Bachelor’s degree in life science, health science, pharmacy, public health, or related field.
  • Strong attention to detail, organizational, and time management skills.
  • Proficiency with Microsoft Office Suite (Excel, Word, PowerPoint).
  • Effective written and verbal communication skills.
  • Ability to learn and apply technical systems and software (EDC, CTMS, etc.).
    Additional Information
    All your information will be kept confidential according to EEO guidelines
Responsibilities
  • Assist in the development, testing, and validation of Electronic Data Capture (EDC) systems and Case Report Forms (CRFs)
  • Support database setup activities including edit check specifications and user acceptance testing (UAT).
  • Review incoming clinical data for completeness, consistency, and accuracy.
  • Generate, track, and resolve data queries in collaboration with clinical sites.
  • Maintain study documentation and data management files.
  • Participate in cross-functional study team meetings and data review discussions.
  • Support Serious Adverse Event (SAE) reconciliation and external data reconciliation (e.g., labs, central imaging).
  • Ensure data management activities follow SOPs, study protocols, and regulatory standards (e.g., ICH-GCP, CDISC).
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