AbbVie
Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing (
AbbVie, North Chicago, Illinois, us, 60086
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 / information needed in preparing internal documents/scientific reports related to clinical trials and to keep multiple reports moving forward simultaneously through multi-tasking.
Description:
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.
Qualifications
*This position is required to sit on-site 3 days/week*
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 or local law:
The compensation range described below is the range of possible base pay compensation that the Company 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 we may ultimately pay 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/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages 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 benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may 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.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
#J-18808-Ljbffr
Job DescriptionPurpose:
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.
Description:
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.
Qualifications
*This position is required to sit on-site 3 days/week*
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 or local law:
The compensation range described below is the range of possible base pay compensation that the Company 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 we may ultimately pay 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/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages 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 benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may 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.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
#J-18808-Ljbffr