Clinical Contract Associate I at Abbott Laboratories Limited

Los Angeles, California, United States -

Full Time

Start Date

Immediate

Expiry Date

31 Jul, 26

Salary

116000.0

Posted On

02 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Contract negotiation, Budget management, Clinical study contracts, Legal terminology, Redlining, Analytical skills, GCP, ICH, GLP, Regulatory compliance, Communication, Microsoft Word, Microsoft Excel, Microsoft Access, Clinical research, Risk mitigation

Industry

Hospitals and Health Care

Description

About Abbott 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. For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring systems, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine ﬁngersticks. We currently have a US office based opening for a Clinical Contract Associate II position with Sylmar, CA or Maple Grove, MN as preferred location. Position Summary Working under the direction of manager or senior contract associate, provides technical assistance in developing, negotiating, reviewing, and processing clinical study and research contracts and budgets. Understands key business drivers and corporate clinical priorities; uses this understanding to accomplish own work. No supervisory responsibilities. Solves problems in straightforward situations; analyzes possible solutions using technical experience, judgment and precedents . Impacts quality of own work and the work of others on the team; works within guidelines and policies. Explains complex information to others in straightforward situations. Capable of routine negotiations with little supervision WHAT YOU’LL DO Under minimal guidance & supervision, develop & negotiate contracts, contract amendments and complex budgets with site partners within expected timelines/metrics Proactively collaborate with external/internal partners to address & resolve contract/budget issues to meet study milestones and deadlines Review informed consents to ensure alignment with contract/agreement and provide guidance to study teams Anticipate potential contract/budget compliance issues and timely risk mitigation EDUCATION AND EXPERIENCE Required Associates Degree (± 13 years) Minimum 1 year related experience Preferred Bachelor's Degree in Business Administration, a related field, or equivalent and/or Paralegal certificate. Negotiations/Skills in redlining documents and analytical experience or equivalent. Familiarity with grant and contract requirements, policies, and procedures including, but not limited to: Knowledge of contract law and legal terminology Understand fundamental legal principles & terminology Clinical and AdvaMed Code of Ethics on Interactions with Health Care Professionals. Knowledge and understanding of GCP, ICH, GLP and other federal, state, industry rules and regulations governing technical aspects of clinical grants and contracts Ensure all required data from studies and sites to comply with regulatory and government requirements (Sunshine Act, FWA, Human Subject Protection training, Clinical Insurance). A demonstrated knowledge of the practices/procedures of the function, company polices, and programs. Demonstrated written and verbal communication, interpersonal, presentation, technical, analytical, statistical, organizational, and follow-up skills, the ability to meet deadlines as well as the ability to converse effectively with all levels of employees. Consistently demonstrates the ability to understand and take effective approaches to varying levels of communication that would be most efficient and productive. Be able to demonstrate and use discretion in exercising work assignments and handle sensitive/confidential information in an effective manner. The demonstrated ability to understand and comply with applicable government regulations and Company operating procedures, processes, policies, and tasks. Demonstrated personal computer skills including a working familiarity with relevant word processing, database, and spreadsheet applications (i.e., Microsoft Word, Excel and Access). Some evaluation, originality, and/or ingenuity WHAT WE OFFER At Abbott, you can have a good job that can grow into a great career. We offer: Training and career development, with onboarding programs for new employees and tuition assistance Financial security through competitive compensation, incentives and retirement plans Health care and well-being programs including medical, dental, vision, wellness and occupational health programs Paid time off 401(k) retirement savings with a generous company match The stability of a company with a record of strong financial performance and history of being actively involved in local communities The base pay for this position is $73,900.00 – $116,000.00. In specific locations, the pay range may vary from the range posted.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

The associate will develop, negotiate, and manage clinical study contracts and complex budgets while collaborating with internal and external partners. They are responsible for ensuring compliance with regulatory requirements and providing guidance to study teams regarding informed consents.