Senior Clinical Contracts Associate

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.

JOB DESCRIPTION:

Senior Clinical Contracts Associate Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree. A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity This position works out of our Sylmar, CA, Santa Clara, CA, Plano, TX or Maple Grove, MN as preferred locations, supporting our medical devices clinical team. This is an in-office position 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 finger-sticks. What You'll Work On Working under the direction of a manager, 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. Under minimal guidance & supervision, develop & negotiate contracts, contract amendments and complex budgets with site partners within expected timelines/metrics Serve as a Business Unit champion/core team member/single point of contact for all study contract & budget-related activities throughout the study life cycle 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. Required Qualifications Bachelor's Degree (± 16 years) In Engineering, Biological Sciences, Nursing, or a related field strongly preferred OR an equivalent combination of education and work experience Minimum 5 years In a clinical research environment or other equivalent experience preferred. Knowledge of regulations and standards (Good Clinical Practices) for conducting clinical research. Ability to travel domestically as needed Polished communicator: written documentation and oral presentations/discussions/meetings Ability to work in a highly matrixed and geographically diverse business environment. Ability to work within a team and as an individual contributor in a fast-paced, changing environment. Ability to leverage and/or engage others to accomplish projects. Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. Multitasks, prioritizes and meets deadlines in timely manner. Strong organizational and follow-up skills, as well as attention to detail Experience and training on GCP Preferred: Working knowledge of imaging modalities, including x-ray, fluoroscopy and MRI Experience with GCP, ISO standards, and clinical trial guidelines Preferred Qualifications Masters Degree (± 18 years) In a relevant discipline/concentration. Sponsor Pharma or Biotech experience preferred. Direct knowledge of Sponsor Clinical Contracting preferred with direct exper #J-18808-Ljbffr Abbott