Principal Associate, Clinical Pharmacology Scientific Support & Reporting Writing

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

Purpose

To build all necessary data/information needed in preparing internal documents/scientific reports related to clinical trials and; to keep multiple reports moving forward simultaneously through multi-tasking.

Responsibilities

• Prepare scientific reports/presentations related to clinical trials using available software and templates and; review/contribute to clinical protocols, by utilizing expertise, to assist in interpretation of data.
• 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 issued by the management regarding clinical studies.
• Apply experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded/un-blinded PK, safety and efficacy reviews and ensure the scientific integrity of all processes.
• Responsible for receiving and completing tasks and assignments from function, Therapeutic Area MD or Scientific Staff within timeline with minimal supervision and; maximizing individual, function/therapeutic area and team productivity.
• Lead the study development by applying most current electronic document conventions/processes most consistently/accurately to ensure scientific integrity of all processes.
• Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management.
• Perform literature/competitive intelligence searches to recognize/resolve scientific and technical problems by applying the