Senior Associate, Clinical Pharmacology Scientific Support  Reporting Writing

📋 Description

• To build all necessary data/information needed in preparing internal documents/scientific reports
• Prepare scientific reports and presentations related to clinical trials using available software
• Assists in constructing phase 1 clinical study planning documents, and writes Phase 1 protocols.
• Review clinical protocols and key decisions impacting project timelines with management.
• Comply with procedures set forth in relevant IQS documents and Study protocols and other directives
• Apply experience to analyze clinical study data, including statistical data using available

🎯 Requirements

• Bachelors/Master’s degree, in Science related to Field with +7 years’ experience in pharmaceutical
• Understanding of clinical study principles
• Must possess good oral and written communication skills
• Must be proficient in using computer to analyze clinical study data, generate reports and create
• Must have knowledge of complex scientific analyses, business-related procedures, and project
• Experience supporting clinical research, drug development and/or therapeutic area operations.

🎁 Benefits

• AbbVie is an equal opportunity employer and is committed to operating with integrity, driving
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