Company Description

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 – 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 X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

PRIMARY FUNCTION/OBJECTIVE
To manage medical research operations and executions including NIS, collaborative research, IIS and PAA in accordance with relevant SOPs and regulatory requirement.

CORE JOB RESPONSIBILITIES

Conduct and manage medical research executions and represent the study operations on multi-functional stakeholders/platforms internally and externallyExecute and oversee medical study operations with stakeholders’ partnership, to ensure all NIS, IIS, PAA, and evidence generation related activities are performed according to corporate, ethical and legal requirementsConduct quality and compliance monitoring in medical research operations, and coordinate with project stakeholders from study start-up to close-out; and ensure execution quality in accordant with SOPsMonitor study data integrity and ensure the successful execution that meets company expectations, with study operation deliverables timely reported per organization requirementsContribute to research core document and agreement management to ensure documentation and communication fulfill GCP, legal and regulatory requirementsContribute to oversee and review study related documents from vendorsSupport in vendor contracting process and managementSupport in study budget planning process for long range planning (LRP), medical planning, medical finance tracking and management and data generation/clinical trials planningSupport in evidence generation related review in terms of publication review & approvalComplies with company training assignments as required
Qualifications

PREFERRED QUALIFICATIONS

Bachelor’s degrees in Pharmacy, Nursing, or relevant scientific discipline. Master’s degree in a scientific discipline will be preferredSignificant clinical research experience for global studies (+ 3 years), and experiences in late phase studies will be preferred, particularly the experiences in Immunology, Oncology, and Neuroscience therapeutic areasExcellent knowledge of clinical research practices, local regulations, and ICH guidelines, with solid experiences in the ethics committee and clinical study contracting processesDemonstrate superior leadership skills to drive project deliverables with good interpersonal and effective communication skills to engage with cross functional stakeholdersCompetent in skills of Project Management, particularly in regard to management of schedule, budget, communication, and qualityFamiliar with managing clinical study vendors and financial activitiesFluent English with excellent verbal and written communication skills
Additional Information

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