Clinical Trial Manager

New

Skills

Clinical Research Regulatory Compliance

Job Overview

Lead planning, conduct, and oversight of operational clinical studies per protocol. Develop study documents, training materials, and trackers. Manage site feasibility, recruitment strategies, and enrollment plans. Monitor metrics and CAPA.

Responsibilities

Lead planning and conduct of clinical studies
Ensure compliance with ICH-GCP, SOPs, and regulatory requirements
Develop study documents and training materials
Drive site feasibility and recruitment strategies
Manage IP handling, drug accountability, and QA coordination

Requirements & Qualifications

Bachelor’s degree in science/health; advanced degree preferred
7+ years of clinical research experience with monitoring
Excellent communication, interpersonal, and organizational skills
MS Office proficiency (Outlook, Word, Excel, PowerPoint)
Deep knowledge of ICH-GCP and regulatory guidelines

Job Type: Remote

Salary: Not Disclosed

Experience: Entry

Duration: 12 Months

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