Abbott Clinical Trial Associate Job | Apply Now
A rare chance has emerged at Abbott for individuals looking to advance their careers in clinical research. The Abbott Clinical Trial Associate position, located in Madison, United States, offers an opportunity to assist in the execution of clinical trials while providing essential project management support. Interested candidates are encouraged to apply promptly.
- Position: Clinical Trial Associate
- Location: Madison, United States
- Category: Regulatory Affairs
About Abbott
Abbott is a global healthcare leader that helps people live more fully at all stages of life. The organization’s portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Abbott’s 122,000 colleagues serve people in more than 160 countries.
Abbott Clinical Trial Associate Job Description
This Abbott Clinical Trial Associate position is responsible for assisting in the execution of clinical trials by providing quality administrative and project management support. The Clinical Trial Associate I will coordinate with all members of the Clinical Affairs team and internal and external stakeholders to successfully execute the clinical study plans of the company.
Eligibility Criteria
- Bachelor’s degree in the life sciences or related field; or Associate’s degree in the life sciences or related field and 2 years of relevant experience in lieu of Bachelor’s degree.
- General knowledge of applicable clinical research principles and requirements, including GCP and ICH guidelines.
- Proficient in using basic software applications including Microsoft Office and various search engines for conducting Internet searches.
- Authorization to work in the United States without sponsorship.
Required Skills
- Demonstrated ability to perform the essential duties of the position with or without accommodation.
- Strong verbal and written communication skills.
- Ability to manage multiple deadlines.
- Excellent attention to detail and organizational skills.
- Ability to work both independently and collaboratively as part of the clinical study team to meet study objectives and timelines.
- Analytical, problem-solving and decision-making skills.
- Ability to exercise judgment and determine appropriate action to a variety of problems of varying complexity.
- Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
Abbott Clinical Trial Associate Job – Key Responsibilities
- Collect essential documents and review for completeness and compliance with Standard Operating Procedures, the protocols, and appropriate regulations; review Trial Master File (TMF) inventory for missing and expiring documents.
- Interact with clinical study sites to support study start-up, execution, and close-out activities.
- Create and maintain study-related trackers, including but not limited to, enrollment, study supplies, receipt of samples, and site information.
- Coordinate the ordering, tracking, and accountability of clinical supplies, including investigational product materials, equipment, and special-order items as requested.
- Review for completeness and route legal documents for execution. File all versions in document management database.
- Draft study documents (study trackers, templates, presentations, etc.) as requested.
- Support case report form (CRF) development, participate in user acceptance testing (UAT) for electronic data systems and review related data management documents, as applicable.
- Represent Abbott as a customer advocate/liaison both internally and externally.
Salary: The base pay for this position is $50,700.00 – $101,300.00. In specific locations, the pay range may vary from the range posted.
This Abbott Clinical Trial Associate opportunity offers a significant step for those interested in clinical research and project management. Qualified candidates are encouraged to apply at the earliest to take advantage of this promising role.
