Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing

About the Company

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.

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 the 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 and provide this information to internal peers and therapeutic area management.
• Perform literature/competitive intelligence searches to recognize/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

• Bachelors/Masters degree in a Science related field with +7 years experience in the pharmaceutical industry.
• Understanding of clinical study principles.
• Must possess good oral and written communication skills.
• Must be proficient in using computers to analyze clinical study data, generate reports, and create presentations, posters, and manuscripts.
• Must have knowledge of complex scientific analyses, business-related procedures, and project leadership.
• Experience supporting clinical research, drug development, and/or therapeutic area operations.
• Must have a 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/experience to analyze clinical study/statistical data by using available software.

Pay

The compensation range described is the range of possible base pay compensation that AbbVie believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and the company may ultimately pay more or less than the posted range. This range may be modified in the future.

Benefits

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