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Clinical Trial Associate

1-3 years
Not Disclosed
10 May 19, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Trial Associate
Location: Redwood City, CA (Hybrid – 3 days/week onsite)
Employment Type: Full-time
Compensation: $60,000 – $85,000 per year


Job Summary:

A fast-growing life sciences company is seeking a motivated and detail-oriented Clinical Trial Associate to support its clinical trial operations. The role involves assisting with site management, trial start-up, monitoring, and closeout activities, while ensuring compliance with regulatory guidelines (ICH GCP, CFR) and internal SOPs.


Key Responsibilities:

  • Provide administrative and operational support for clinical trials in line with SOPs, timelines, budgets, and regulatory requirements.

  • Manage and track clinical trial supplies including preparation, shipping, and inventory control.

  • Assist in preparing materials for investigator meetings, internal team meetings, and study manuals.

  • Maintain study-specific trackers and documents such as site enrollment, regulatory submissions, activation statuses, and sample logistics.

  • Coordinate meetings, including scheduling and preparing meeting minutes.

  • Support the creation and upkeep of trial-specific tools and documentation.

  • Perform additional duties as required to ensure project success and team efficiency.


Qualifications:

  • Bachelor’s degree in a scientific or healthcare-related field preferred.

  • 1–3 years of relevant clinical trial experience, preferably in the pharmaceutical, biotech, or CRO environment.

  • Familiarity with ICH GCP and clinical research regulations preferred.

  • Understanding of clinical trial and drug development processes.

  • Exceptional attention to detail and follow-through.

  • Proficient in Microsoft Office (Outlook, Word, PowerPoint, Excel).

  • Strong organizational and time management skills; able to prioritize in a fast-paced environment.

  • Excellent communication skills, both written and verbal.