
Clinical Research Coordinator Joulé
- $26–$30 Per Hour
| Location | Plano, Texas |
| Industry | Healthcare Services |
| Salary | $61,300–$122,700 Per Year |
| Company Size | 10,000 employees or more |
| Year Founded | 1910 |
| Website | http://www.abbott.com/ |
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,nutritionalsand branded generic medicines.
For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whetherit’sglucose 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 than10,000 peoplehave healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than500,000 peoplewith diabetes from routinengersticks.
We currently have a USoffice basedopening for aSr.Clinical Contract Associatepositionwith Sylmar, CA, Santa Clara, CA, Plano, TXor Maple Grove, MN as preferred location.This is an in-office position
Position Summary
Working under the direction of manager, provides technicalassistancein developing, negotiating, reviewing, and processing clinical study and research contracts and budgets. Understands key business drivers and corporate clinical priorities; uses this understanding toaccomplishownwork. No supervisory responsibilities.Solvesproblems in straightforward situations;analyzespossible solutionsusing technical experience,judgmentandprecedents.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, contractamendmentsand complex budgets with site partners within expected timelines/metrics
Servesas a Business Unit champion/core team member/single point of contact for all study contract & budget related activities throughout the studylife 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 andtimelyrisk mitigation
EDUCATION AND EXPERIENCE
BachelorsDegree (± 16 years) In Engineering, Biological Sciences, Nursing, or a related field strongly preferred OR an equivalent combination of education and work experience
MastersDegree (± 18 years) In a relevant discipline/concentration.
Minimum 5yearsIna clinical research environment or other equivalent experience preferred. Knowledge of regulations and standards (Good Clinical Practices) for conducting clinical research.
Ability to travel domesticallyas 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 toleverageand/or engage othersto accomplishprojects.
Strong verbal and written communications withabilityto effectively communicate at multiple levels in the organization.
Multitasks,prioritizesand meets deadlines intimelymanner.
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,fluoroscopyand MRI Experience with GCP, ISO standards, and clinical trial guidelines
Preferred
Bachelor's Degree in Business Administration,a relatedfield, or equivalent.
Sponsor Pharma or Biotech experience preferred. Direct knowledge of Sponsor Clinical
Contracting preferredwith direct experience innegotiating contract language & complex budgets
BudgetDevelopmentexperience
Advanced Excel experience
Experience withPower BIwould be preferred
WHAT WE OFFER
At Abbott, you can havea good jobthat can grow intoa great career. We offer:
Training and career development, with onboarding programs for new employees and tuitionassistance
Financial securitythrough competitive compensation,incentivesand retirement plans
Health care and well-being programsincluding medical, dental, vision,wellnessand occupational health programs
Paid time off
401(k)retirement savings with a generous company match
The stability of a companywith a record of strong financial performance and history of being actively involved in local communities
The base pay for this position is
$61,300.00 – $122,700.00In specific locations, the pay range may vary from the range posted.
At Abbott, we are enthusiastic, energetic and committed to doing great work every day. Our employees are passionate about helping to translate science into lasting contributions to health care and the health of people worldwide. At the heart of our organization is our "Promise for Life"—a statement that embodies our company's commitment to employees, shareholders, local communities and the people who depend on our company and products to live healthier lives.
Vital to our promise is the speed in which we act, respond and deliver. As Abbott employees, we are ready to meet change and challenges head-on. As a result, we are a company that adapts quickly, and through our passion for innovation we are able to continually create a pipeline of products that help improve the length and quality of life around the world.
We are proud of our rich, more than 120-year history. We continue to be driven to advance leading-edge science and technologies, support diversity, focus on exceptional performance and earn the trust of those we serve.

