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Clinical Research Coordinator 2

2+ years
$40 - $45/hour
10 March 4, 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

Clinical Research Coordinator 2

Location: Palo Alto, CA
Employment Type: On-site, Contract
Salary: $40/hr - $45/hr
Posted: 4 days ago

Job Overview:

Join a top-tier research team conducting clinical trials to develop groundbreaking therapies for allergic disorders. This role involves working with a diverse patient population to improve treatments and uncover lasting cures.

Key Responsibilities:

  • Develop and implement strategies to attract and retain participants for long-term clinical trials.
  • Oversee data collection, organization, reporting, and monitoring to ensure accuracy and compliance.
  • Manage study schedules, set targets, track progress, and ensure accountability.
  • Extract, analyze, and interpret research data to support study objectives.
  • Lead team meetings, document key decisions, and drive action plans.
  • Collaborate with principal investigators, study sponsors, and regulatory bodies to resolve queries and report adverse events.
  • Identify and implement best practices to enhance research efficiency and workflow.
  • Develop and manage study budgets, distinguishing standard care from research procedures.
  • Track patient progress and study milestones while invoicing sponsors per contract terms.
  • Ensure compliance with Institutional Review Board (IRB) and regulatory requirements, including timely renewals.

Key Qualifications:

  • Education: Bachelor's degree required.
  • Experience: Minimum 2 years of experience in clinical research.
  • Skills:
    • Strong data management, analytical, and organizational skills.
    • Ability to lead meetings, document key decisions, and drive action plans.
    • Excellent communication and problem-solving abilities.
    • Experience working with IRB protocols and regulatory submissions.

Why Join?

  • Work with a leading research team on impactful clinical trials.
  • Competitive salary and comprehensive benefits (Medical Insurance, 401K).
  • Opportunity for career growth in a prestigious research environment.