Clinical Research Associate - 30265BR - EN in Remote, OR at Stryker Corporation

Date Posted: 6/1/2018

Job Snapshot

Job Description

Who we want

Collaborators. Collaborates and builds relationships with internal and external stakeholders
Achievers. Thrives on accomplishing tasks and constantly driven to do more
Communicators. Articulates well and expresses ideas effectively
Teammates. Partners who listen to ideas, share thoughts and work together to move the business forward
Professionals. Committed to quality and integrity

What you will do

We are looking for a solutions focused team player who is prepared to take on a challenging role in the conduct and management of clinical research. As a Clinical Research Associate (CRA), you will interact directly with institutions and investigators, and will drive research initiatives and ensure alignment with strategic goals. You will be responsible for tasks that require a high degree of attention to detail and accuracy. You will be working with an international team of colleagues and investigators who are driven to deliver high quality results that make an impact on the quality of healthcare around the world.
  • Work in a virtual team environment, requiring that you be highly engaged, communicate effectively and maintain accurate and timely tracking and documentation
  • Take lead roles in the development and execution of studies designed to support clinical evidence of device safety and performance
  • Demonstrate excellent organizational, decision-making, and time management skills in a fast-paced environment
  • Build and maintain excellent working relationships with KOLs and colleagues
  • Coordinate and execute research projects, including clinical study plan and protocol development, contracting, auditing and monitoring, and close-out activities
  • Ensure operational aspects of the studies are being conducted in accordance with all relevant ethical and government standards, GCPs, and Stryker Standard Operating Procedures.
  • Maintain a high level of professional expertise through familiarity with scientific literature, product portfolio, and the competitive and healthcare environments.

Job Requirements

What you need
  • Bachelor’s Degree in Health Sciences or other related technical discipline
  • 2+ years’ experience in a clinical study administration role or other related professional role
  • Fundamental knowledge and good understanding of GCPs, clinical study development process, and logistics; Certificate Degree in Clinical Research or CCRA (Certified Clinical Research Associate) credentials preferred




Qualifications
  • Bachelor’s Degree in Health Sciences or other related technical discipline
  • 2+ years’ experience in a clinical study administration role or other related professional role
  • Fundamental knowledge and good understanding of GCPs, clinical study development process, and logistics
  • Excellent communication skills (both written and oral) and the ability to build effective relationships
  • Excellent organizational and planning skills
  • Consistent attention to detail and follow through on commitments
  • Excellent interpersonal, judgment, and time management skills
  • Demonstrated ability to multi-task and think on your feet
  • Demonstrated IT and administrative skills
  • Virtual team-based work experience is essential
  • Proficient knowledge of orthopedic procedures and terminology
  • Prior experience executing medical device research studies
  • Prior experience working in a regulated environment
  • Ability to travel up to 40%
  • CRA certification (ICR/ACRP/SOCRA) or eligible to take certification exam is desirable
  • Proficient in the use of MS Office programs: Project, Excel, Word, PowerPoint

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