Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing

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 including immunology, oncology and neuroscience—and products and services in our Allergan Aesthetics portfolio.

About the role

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

Responsibilities

• Prepare scientific reports and presentations related to clinical trials using available software and templates.
• Assist in constructing Phase 1 clinical study planning documents, and write 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 management regarding clinical/preclinical studies.
• Apply experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded efficacy and safety reviews and ensure the scientific integrity of all processes.
• Responsible for receiving and completing tasks and assignments from Therapeutic Area MD or Scientific Staff within timeline with minimal supervision.
• Ensure scientific integrity of all processes by applying current electronic document conventions and processes consistently and accurately.
• Integrate clinical trial data across studies and identify issues impacting projects, providing this information to internal peers and therapeutic area management.
• Perform literature and competitive intelligence searches to recognize and resolve scientific and technical problems by applying the most current electronic document conventions and processes consistently and accurately.
• Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management.
• Responsible for maximizing individual, therapeutic area, and team productivity; and mentor therapeutic area personnel.

Requirements

• Bachelor’s or Master’s degree in a science-related field with +7 years’ experience in the pharmaceutical industry.
• Understanding of clinical study principles.
• Good oral and written communication skills.
• Proficient in using computers to analyze clinical study data, generate reports, and create presentations, posters, and manuscripts.
• Knowledge of complex scientific analyses, business-related procedures, and project leadership.
• Experience supporting clinical research, drug development, and/or therapeutic area operations.
• Proven record of successful projects.
• Ability to produce work of the highest quality by paying attention to detail.
• Ability to appropriately and effectively use resources to complete tasks and meet required timelines.
• Independent expertise and experience to analyze clinical study and statistical data using available software.

Benefits

• Comprehensive package of benefits including paid time off (vacation, holidays, sick).
• Medical, dental, and vision insurance.
• 401(k) retirement plan.
• Eligibility to participate in short-term incentive programs.