Job Description
Hybrid (3x per week onsite) in Irvine, CA strongly preferred.
Responsibilities
- Prepares scientific reports and presentations using available software and templates.
- Reviews and contributes to clinical protocols.
- Utilizes expertise to assist in interpretation of data.
- Brings together all necessary data and information to prepare internal documents or scientific reports; keep multiple reports moving forward simultaneously (multi-tasking).
- Coordinates advisory meetings and consulting agreements.
- Complies with procedures set forth in relevant IQS documents, study protocols, other directives issued by the management regarding clinical / pre-clinical studies.
- Ensures scientific integrity of all processes.
- Leads the development of and applies the most current electronic document conventions and processes consistently and accurately.
- Provides / presents key clinical study information to therapeutic area and management.
- Committed to producing work of the highest quality.
Pays close attention to detail.
Qualifications
- Bachelor's / Master's degree in Science related to field with 11+ years of experience in the pharmaceutical industry or PharmD / PhD with 1+ years.
- Experience in eye care space strongly preferred.
- Understanding of complex clinical study principles.
- Possesses good oral and written communication skills.
- Advanced understanding of appropriate technology necessary to analyze clinical study data, generate reports and create presentations, posters and manuscripts.
- Team, drug development, and scientific project leadership or related experience.
- Experience supporting clinical research, drug development and / or therapeutic area operations. Proven record of successful projects brought to completion.
- Requires multi-faceted, broad-based experience in multiple therapeutic areas or clinical functions. Must have in-depth knowledge of clinical study issues.
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.
This job is eligible to participate in our long-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.
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US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more :
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