• Full Time
  • Mentor, OH
  • Applications have closed

Website Avery Dennison

Clinical Research Associate

  • 7070 Spinach Dr, Mentor, OH 44060, USA
  • Full-time

Company Description

Avery Dennison Corporation (NYSE: AVY) is a global materials science and manufacturing company specializing in the design and manufacture of a wide variety of labeling and functional materials. The company’s products, which are used in nearly every major industry, include pressure-sensitive materials for labels and graphic applications; tapes and other bonding solutions for industrial, medical and retail applications; tags, labels and embellishments for apparel; and radio-frequency identification (RFID) solutions serving retail apparel and other markets. Headquartered in Glendale, California, the company employs approximately 30,000 employees in more than 50 countries. Reported sales in 2018 were $7.2 billion. Learn more at www.averydennison.com.

Job Description

Avery Dennison is currently seeking a Clinical Research Associate to contribute to new product research and development teams of our Vancive Medical Technology business with responsibility for clinical and pre-clinical research studies throughout the entire design cycle from early concept/research through to formal validation and claims substantiation. You will join a growing team that is part of the high-value segment focus within Avery Dennison.

Primary Responsibilities and Essential Job Functions:

  • Work to understand customer and user requirements from a clinical perspective. Identify relevant design characteristics and critical performance requirements, then formulate practical research study protocols for efficiently testing product designs against them.
  • Organize and carry out research studies on schedule per project deadline. Duties include authoring protocols, recruiting subjects, coordinating testing schedules, tracking and reporting on progress of study metrics, gathering and analyzing data, and reporting results.
  • Conduct human-subjects research in compliance with relevant guidelines and regulations for Good Clinical Practice (GCP)
  • Apply standard statistical techniques for protocol design and data analysis.
  • Conduct systematic scientific literature reviews. Assimilate data to draw conclusions, and document the results.
  • Communicate research results in a variety of formats including technical reports, customer presentations, conference abstracts, white papers, marketing materials, and the like.
  • Foster relationships with external partners such as contract research organizations, clinicians, academic research labs, and the like.
  • Support new product development within assigned projects in collaborative relationship with all cross functional teams (R&D, Marketing, Regulatory Affairs etc).
  • Understand and follow cGMP, ISO 13485, ISO 11607, and FDA 21 CFR Part 820 regulations.
  • Perform other duties as assigned.

Qualifications

Required:

  • Bachelor’s degree in a biomedical, health science, or related discipline.
  • Excellent organizational skills
  • Excellent interpersonal skills
  • Excellent writing and communication skills
  • Biomedical research experience or medical/clinical experience

Preferred:

  • Master’s degree in a biomedical science or health science
  • License such as RN, LPN, MD.
  • Clinical research certification from SoCRA, ACRP, or the like

Avery Dennison is an Equal Opportunity Employer.

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Additional Information

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, protected veteran status or other protected status. EEOE/M/F/Vet/Disabled. All your information will be kept confidential according to EEO guidelines