Technician, ACPRU Clinical Research I

About AbbVie
AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its 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 Details: Reviews protocols and provides input on study-specific activities that impact technical areas of
responsibility and ACPRU workflow in relation to other studies planned to occur concurrently.
Maintains professional communications and interactions with ACPRU personnel, study subjects,
and other internal/external departments and keeps Management abreast of issues as appropriate.
Maintains accurate and complete source data in PIMS and/or other source documents and assists
in the resolution of source discrepancies or issues, as appropriate.
Performs study-related protocol activities, i.e. ECGs, blood draws, meals, etc. as assigned.
Maintains safety and confidentiality of study subjects, accurately communicates confidential safety
related information, and ensures that staff can recognize safety related events as appropriate, and
ensures information is passed along to the next work shift.
Mentors Clinical Research Technicians, identifies training needs and conducts training as
appropriate. Participates in quality and compliance improvement projects and provides feedback as
subject matter expert.
Understands and complies with SOPs, FDA regulations, GCP requirements, identifies potential risk
of compliance deficiencies, and provides feedback as appropriate.
Performs pre-study setup i.e. activity schedule, document preparation, laboratory set-up, label
preparation, lab ordering, performance of QC checks.
Leads Clinical Research Technicians on daily activities to ensure study related protocol events are
completed and work closely with management for adjustments to staff schedules if necessary, and
performs other duties as assigned.
Works under minimal direction of supervisor.

Shift : Tue-Thu 1^st or 2^nd shift , Friday and Saturday  3rd shift. 

Qualifications

Associate Degree or equivalent relevant experience.
2-6 years of medical/lab technology experience and/or
2-6 years of clinical or research experience.
Communication Skills – Ability to concisely communicate key issues to stakeholders
Analytical Skills – Ability to assess issues that arise, seek multiple perspectives, gather more
information as needed, and identify key issues that need to be addressed

Significant Work Activities
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel
No
Job Type
Experienced
Schedule
Full-time
Job Level Code
IC
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis 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, protected veteran status, or any other legally protected characteristic.