Clinical Research Associate at ZimVie US Corp LLC Palm Beach Gardens, FL

ZimVie US Corp LLC

Palm Beach Gardens, FLFull-timePosted May 1, 2026

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Qualifications

  • •Expected Areas of Competence (i.e., knowledge, skills, and abilities)
  • •Ability to foster positive working relationships with a wide variety of internal and external personalities
  • •Demonstrates a drive for continuous learning and continuous improvement
  • •Balances an attention to detail with the overarching strategy
  • •Proficient in Microsoft Office Suite
  • •Knowledge of regulations governing clinical studies including GCP (Good Clinical Practices), PHRP (protecting human research participants), and HIPAA principles
  • •B.S. Degree in the health, life sciences, or engineering disciplines, or equivalent experience plus 3-5 years experience working in a clinical research environment, or an equivalent combination of education and experience
  • •4 more items(s)

Responsibilities

  • •Responsible for supporting study management and data reports for clinical trials being conducted by the Scientific Affairs team
  • •Clinical study responsibilities include tracking and communicating the ongoing operation performance of each active study and study site
  • •Additional areas of responsibility include supporting business needs in the areas of new product development teams, extended claims, and operation/execution of new clinical trials
  • •This role reports to the Scientific Affairs Manager and primary responsibilities include:
  • •Assists the trial manager in all aspects of trial development and initiation such as contract management, payment tracking, remote monitoring, study binder management and regular reporting to all active sites
  • •Case report form (CRF) development and revision as necessary
  • •Maintenance of the Sponsor’s Trial Master File
  • •Remote data quality monitoring and query resolution with Site(s)
  • •Enrollment, intervention, and follow-up tracking of all study patients
  • •Coordinates all regulatory activities for both active and future investigators under the direction of the Scientific Affairs Manager
  • •May perform onsite monitoring activities either independently or in conjunction with the trial manager or contract monitor
  • •Assists the trial manager with the review and compilation of data and prepared reports as needed for regulatory agencies, IRBs, investigative sites, or notified bodies
  • •May assist or independently perform literature reviews as needed for protocol development, complaint handling, new product development, or in support of regulatory submissions
  • •This is not an exhaustive list of duties or functions and may not necessarily comprise all of the "essential functions" for purposes of the ADA
  • •11 more items(s)
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