Job Details

Stryker

http://www.stryker.com

Senior Clinical Research Associate (Remote)

Occupation: Science and Research

Specialty: Clinical Research

Visa sponsorship provided: No

Location: Virtual, Louisiana, United States

Why join Stryker?

We are proud to be named one of the World’s Best Workplaces and a Best Workplace for Diversity by Fortune Magazine! Learn more about our award-winning organization by visiting stryker.com

Our benefits include bonuses; commissions; healthcare; insurance benefits; retirement programs; stock based plans; paid time off plans; family and parenting leaves; tuition reimbursement; wellness programs; onsite fitness centers and cafeterias; discount purchase programs; and service and performance awards – not to mention various social and recreational activities.

Stryker Neurovascular is seeking to hire a Senior Clinical Research Associate to be based in Fremont, CA or remotely anywhere in the United States. As a Senior CRA you will work on Medical Device Clinical trials, traveling 30-40% within the US.

Stryker’s Neurovascular division is focused on advancing the practice of less invasive stroke therapies. Watch this video to see how Stryker is making a difference: https://www.youtube.com/watch?v=JANFZrpt1Hg.

Why come to Stryker? Dozens of Reasons To Love Stryker

Stryker will offer you a competitive total rewards package, including competitive base salary, performance bonus, and benefits. We also offer other non-financial rewards, and engaging work environment and meaningful career advancement opportunity. Stryker Benefits

WHO WE WANT:

Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.
Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.

WHAT YOU WILL DO:

As the Senior Clinical Research Associate, you work with program management, delivering site monitoring and management for the study operations team.

Communicate with investigators, colleagues, and vendors ensuring clinical quality and compliance.
Provides sponsor oversight of sites and mentorship to junior team members.
Supports various phases of clinical studies (i.e., study planning, site qualification and investigator selection, monitoring, closeout, etc.).
Oversees contract research organization personnel site activities and vendor performance.
Supports the development of clinical study plans, presentations, study documents, contracts, development, and design of case report forms.
Leads review of clinical data listings for accuracy and escalates issues to the clinical project manager.
Develops and implements enrollment and recruitment strategies.
Reviews monitoring visit reports and tracks resolution of action items.
Identifies noncompliance and implements preventative and corrective actions.

WHAT YOU NEED:

Bachelor’s Degree - required
4+ years relevant work experience in a clinical study operations role - required
3+ years Clinical Research Associate (CRA) site management and clinical research monitoring experience - required
Working knowledge of GCP/ICH guidelines, federal and local regulations - required.

This job may be performed remotely from anywhere in the United States, except that this job may not be filled or performed in Colorado.

Know someone at Stryker?

Be sure to have them submit you as a referral prior to applying for this position. Learn more about our employee referral program at https://careers.stryker.com/referrals/

About Stryker

Stryker is one of the world’s leading medical technology companies and, together with our customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes.