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Analyst - Clinical Trial Coordinator

2+ years
Not Disclosed
10 Feb. 6, 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

Analyst - Clinical Trial Coordinator

📍 Location: [Location not specified]
🗓️ Posted: [Date not specified]

About the Position:

As an Analyst - Clinical Trial Coordinator, you will be a key contributor to the execution and management of clinical trials. This role involves supporting various administrative and operational aspects of clinical trials, including coordination of timelines, resources, and communication between cross-functional teams to ensure the timely and efficient conduct of clinical trials in compliance with applicable regulatory requirements.

Key Responsibilities:

  • Assist with the preparation, coordination, and management of clinical trial documentation.
  • Support the execution of clinical trial protocols and ensure adherence to regulatory standards.
  • Maintain communication with internal teams and external partners (e.g., clinical research sites, vendors).
  • Coordinate and track the progress of clinical trials, ensuring that all deliverables are met on time and within budget.
  • Support the collection and organization of clinical trial data and documentation.
  • Assist in monitoring clinical trial performance and identifying areas for improvement.
  • Collaborate with cross-functional teams, including project management, clinical operations, and regulatory affairs.

Qualifications:

  • Education: Bachelor’s degree in life sciences, clinical research, or a related field (or equivalent experience).
  • Experience: Previous experience in clinical trials, preferably in a coordinating or supporting role.
  • Skills:
    • Strong organizational and communication skills.
    • Ability to manage multiple tasks and prioritize effectively.
    • Familiarity with clinical trial protocols and regulations.
    • Proficiency in Microsoft Office and other relevant software/tools.

Why Join:

As an Analyst - Clinical Trial Coordinator, you will be part of a dynamic team that plays a critical role in the advancement of clinical research and the development of new treatments. You will have the opportunity to work in a collaborative environment, learning from experienced professionals, and contributing to the success of clinical trials that could ultimately make a significant impact on patient care.

How to Apply:

Please submit your application as instructed in the job posting (CV, cover letter, etc.).