Clinical Research Associate II

JOB DESCRIPTION:

Clinical Research Associate II

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. Youll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify forfree medical coverage in ourHealth Investment Plan (HIP) PPOmedical 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 bachelors 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

The CRA II will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality standards.

This position will be based in our Alameda CA office.

What Youll Work On

• Conduct single or multi-center medical device clinical studies.
• Perform study site visits (SQV SIV IMV COV) generate monitoring trip reports and track resolution of action items.
• Participate in study start up activities.
• Responsible for shipping study devices and supplies to clinical sites and performing study device accountability.
• Manage clinical monitoring activities and overall site management ensuring compliance to the Study Protocol Good Clinical Practices (GCPs) ICH guidelines Federal Regulations department procedures and applicable regulatory requirements.
• Responsible for assisting senior staff in planning study conduct designing case report forms (CRFs) conducting User Acceptance Testing (UAT) Contract Research Organization (CRO) selection and management selection and training of investigator sites planning and running study meetings evaluation selection and training of new study investigators and writing and assembling submissions.
• Maintain and audit Trial Master File to ensure inspection readiness.
• Perform review of clinical data listings for completeness and accuracy and escalate issues to the Clinical Operations Manager as needed.
• Participate in cross-functional clinical team(s) in the planning and execution of clinical trials.
• Proactively and effectively communicate the status of clinical studies to management.
• Ensures quality delivery of study deliverables within agreed budgets and timelines.
• Participatein the interim and final reviews of study data in preparation of regulatory submissions.
• Involvedin the preparation of all applicable documents required for the conduct of the study (such as Trial Master File (TMF) Clinical Protocols and Reports).
• May interact with RA/QA in responding to audits and FDA inquiries.

Required Qualifications

• B.S. degree in life sciences or equivalent with minimum 5 years of clinical research experience.
• Must have 2 years of relevant experience in site monitoring.
• Experience in conducting medical device and/or in-vitro diagnostics studies preferred. Pharmaceutical background may also be considered.
• Must be able to travel 30-50%.

Preferred Qualifications

• Demonstrated excellence in teamwork shared mindset for success stellar interpersonal and communication skills including building rapport with team members peers and management.
• Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation.
• Must have a demonstrated ability to solve problems with innovative solutions along with strong project management and organizational skills to deliver projects on time and on budget.
• Able to manage numerous projects/conflicting priorities and to be flexible when priorities change.
• Working knowledge of GCP Clinical and Regulatory Affairs.
• Proficient with Microsoft Suite.

Learn more about our health and wellness benefits which provide the security to help you and your family live full lives:

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer committed to employee diversity.

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Divisional Information

Medical Devices

General Medical Devices:

Our medical devices help more than 10000 people have healthier hearts improve quality of life for thousands of people living with chronic pain and movement disorders and liberate more than 500000 people with diabetes from routine fingersticks.

CRM

As a global leader in Cardiac Rhythm Technologies we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias or irregular heartbeats.

Diabetes

Were focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. Were revolutionizing the way people monitor their glucose levels with our new sensing technology.

Vascular

Abbott Vascular provides innovative minimally invasive and cost-effective products for the treatment of vascular disease.

Neuromodulation

Our Neuromodulation business includes implantable devices compatible with mobile technology to help people who suffer from chronic pain and movement disorders. These non-opioid therapies allow us to provide interventional pain therapy to patients throughout the pain continuum.

Structural Heart

Structural Heart Business Mission: Why We Exist

Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease.

EP

In Abbotts Electrophysiology (EP) business were advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation allowing people to restore their health and get on with their lives.

HF

In Abbotts Heart Failure (HF) business were developing solutions to diagnose monitor and manage heart failure allowing people to restore their health and get on with their lives.

Diagnostics

Were empowering smarter medical and economic decision-making to help transform the way people manage their health at all stages of life. Every day more than 10 million tests are run on Abbotts diagnostics instruments providing lab results for millions of people.

Our Point of Care diagnostic portfolio spans key health and therapeutic areas including infectious disease cardiometabolic informatics and toxicology.

Our diagnostic solutions are used in hospitals laboratories and clinics around the globe. The crucial information derived from our tests instruments and informatics systems is often the first step in patient care decision-making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers.

Our rapid diagnostics solutions are helping address some of the worlds greatest healthcare challenges.

Our molecular division delivers best-in-class innovative testing solutions for people around the world to provide answers to lifes critical health decisions. We help people live full and healthy lives through our accessible molecular-based solutions.

Nutrition

Our nutrition business develops science-based nutrition products for people of all ages from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands including Similac PediaSure Pedialyte Ensure and Glucerna to help them get the nutrients they need to live their healthiest lives.

The base pay for this position is

In specific locations the pay range may vary from the range posted.

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