Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing

Company Description About AbbVie 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. For more information about AbbVie, please visit us at Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube. Job Description 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 and presentations related to clinical trials using available software and templates. 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/ 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. Qualifications Bachelors/Master’s degree, in Science related to Field with +7 years’ experience in pharmaceutical industry 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 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. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law: The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographiclocation,andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees. This job is eligible toparticipatein our short-term incentiveprograms. Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: #J-18808-Ljbffr Allergan