Allergan
Associate II, Clinical Pharmacology Scientific Support & Reporting (Hybrid, IL B
Allergan, Lincoln, Nebraska, United States, 68511
Company DescriptionAbbVie'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 Twitter , Facebook , Instagram , YouTube and LinkedIn .
Job DescriptionPurpose:To build all necessary data and information needed to prepare internal documents/scientific reports related to clinical trials and keep multiple reports moving forward simultaneously through multi-tasking.Responsibilities:Prepare scientific reports and presentations related to clinical trials using available software and templates.Responsible for writing basic protocols and clinical study report.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.Responsible for receiving and completing tasks and assignments from function or Therapeutic Area MD or Scientific Staff within timeline with minimal supervisionPerform literature and competitive intelligence searchesEnsure scientific integrity of all processes by applying current electronic document conventions and processes consistently and accurately.Integrate clinical trial data across studies, identify issues impacting projects and provide the relevant information to internal peers and therapeutic area management.Appropriate and effective use of resources to complete tasks and meet required timelines.Responsible for maximizing individual, function/therapeutic area and team productivity; and mentor function/therapeutic area personnel.
Qualifications*This position will be required to sit on-site 3 days / week*Bachelors/Master’s degree, in Science related to Field, with +5 years’ experience in pharmaceutical industryAssociates degree/RN with 9+ years of experience in pharmaceutical industry may be additionally consideredUnderstanding of basic clinical study principlesMust possess good oral and written communication skillsProficient in using computer to analyze clinical study data, generate reports and create presentationsExperience supporting clinical research, drug development and/or function/therapeutic area operations.Must have proven record of successful projects.Must be able to produce work of highest quality by paying attention to detailAbility to identify opportunities and participate in process improvement initiatives.
Additional InformationApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:The compensation range described below is the range of possible base pay compensation that the Company believes ingood faith it will pay for this role at the time of this posting based on the job grade for this position. Individualcompensation paid within this range will depend on many factors including geographic location, and we may ultimatelypay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/visioninsurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, and determinable.The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay be modified at the Company’s sole and absolute discretion, consistent with applicable law.AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.html
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Job DescriptionPurpose:To build all necessary data and information needed to prepare internal documents/scientific reports related to clinical trials and keep multiple reports moving forward simultaneously through multi-tasking.Responsibilities:Prepare scientific reports and presentations related to clinical trials using available software and templates.Responsible for writing basic protocols and clinical study report.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.Responsible for receiving and completing tasks and assignments from function or Therapeutic Area MD or Scientific Staff within timeline with minimal supervisionPerform literature and competitive intelligence searchesEnsure scientific integrity of all processes by applying current electronic document conventions and processes consistently and accurately.Integrate clinical trial data across studies, identify issues impacting projects and provide the relevant information to internal peers and therapeutic area management.Appropriate and effective use of resources to complete tasks and meet required timelines.Responsible for maximizing individual, function/therapeutic area and team productivity; and mentor function/therapeutic area personnel.
Qualifications*This position will be required to sit on-site 3 days / week*Bachelors/Master’s degree, in Science related to Field, with +5 years’ experience in pharmaceutical industryAssociates degree/RN with 9+ years of experience in pharmaceutical industry may be additionally consideredUnderstanding of basic clinical study principlesMust possess good oral and written communication skillsProficient in using computer to analyze clinical study data, generate reports and create presentationsExperience supporting clinical research, drug development and/or function/therapeutic area operations.Must have proven record of successful projects.Must be able to produce work of highest quality by paying attention to detailAbility to identify opportunities and participate in process improvement initiatives.
Additional InformationApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:The compensation range described below is the range of possible base pay compensation that the Company believes ingood faith it will pay for this role at the time of this posting based on the job grade for this position. Individualcompensation paid within this range will depend on many factors including geographic location, and we may ultimatelypay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/visioninsurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, and determinable.The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay be modified at the Company’s sole and absolute discretion, consistent with applicable law.AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.html
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