Clinical Trial Associate I

Abbott; Madison (WI); On-site; USD 51,000 - 101,000; Full time

Job summary

Abbott in Madison, Wisconsin is seeking a Clinical Trial Assistant to support the execution of clinical studies with quality administrative and project management tasks.

You will coordinate with the Clinical Affairs team and internal/external stakeholders to successfully execute study plans, maintain trackers, and support site start-up, execution, and close-out activities.

Qualifications

• Degree in life sciences or related field and relevant experience.
• GCP and ICH guidelines knowledge required.
• Proficient with MS Office and internet research.
• Ability to perform duties with or without accommodation.

Responsibilities

• Assist in execution of clinical trials with admin and project support.
• Coordinate with Clinical Affairs team and stakeholders for study plans.
• Create and maintain study trackers and site information.
• Coordinate supply orders, including investigational products and equipment.
• Review documents for completeness and route for execution.
• Draft study documents and support CRF development and UAT.

Skills

GCP knowledge

ICH guidelines

MS Office proficiency

Strong communication

Education

Bachelor’s degree in life sciences

Associate degree +2 years experience

Tools

Clinical Trial Management System

TMF documentation tools

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

The Opportunity

This position is responsible for assisting in the execution of clinical trials by providing quality administrative and project management support. This position 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.

What You’ll Work On

• 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.
• Coordinate study start-up, execution, and close-out activities, or Investigator Meetings, as requested.
• Responsible for completing assigned tasks to support study timelines and metrics with minimal ongoing direction.
• Identify and report problems, investigate alternatives, and make recommendations for resolution and process improvements.
• Responsible for organizing cross-functional project meetings. Distribute agendas, take and distribute meeting minutes.
• Provide follow-up support and data collection for Research and Development teams to advance project objectives.
• Initiate purchase requests liaise with Accounts Payable and vendors as needed.
• Provide support to Clinical Trial Manager for clinical study budget review, tracking, and maintenance.
• Must be able to work both independently and collaboratively as part of the clinical study team to meet study objectives and timelines.
• Author and provide input to Clinical Affairs business processes.
• Maintain a working understanding of current SOPs, work instructions, applicable regulations, and guidance documents, such as FDA Code of Federal Regulations (CFR) and International Council on Harmonisation (ICH), Guideline for Good Clinical Practices (GCP).
• Maintain applicable clinical study data in Clinical Trial Management System.
• Ability to organize, present, and convey problems or issues.
• Strong verbal and written communication skills.
• Effective presentation skills.
• Ability to interface and work effectively within team and department with changing priorities.
• Ability to frequently and accurately communicate with co-workers, customers, and vendors, via the telephone or by email.
• Ability to exercise judgment and determine appropriate action to a variety of problems of varying complexity.
• Ability to manage multiple deadlines.
• Analytical, problem solving and decision-making skills.
• Excellent attention to detail and organizational skills.
• Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
• Support and comply with the company’s Quality Management System policies and procedures.
• Maintain regular and reliable attendance.
• Ability to act with an inclusion mindset and model these behaviors for the organization.
• Ability to work designated schedule.
• Ability to work nights and/or weekends.
• Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.
• Ability to travel 5% of working time away from work location, may include overnight/weekend travel.

Required Qualifications

• Bachelor’s degree in the life sciences or related field; or Associates 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 (Word - generate documents and tables, Excel - create and modify spreadsheets, create complex formulas, etc., Email – preferably Outlook) and various search engines for conducting Internet searches.
• Demonstrated ability to perform the essential duties of the position with or without accommodation.
• Authorization to work in the United States without sponsorship.

Preferred Qualifications

• 1+ year of experience in a clinical research setting (Clinical Trial Assistant, Study Coordinator, or similar).
• Experience in a healthcare, clinical, or science related field.

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.