Johnson & Johnson Karrieren

In-House Clinical Research Associate

Ettlingen, Deutschland
Clinical Research non-MD


Requisition ID: 1805691004W

Johnson & Johnson Surgical Vision is committed to improving and restoring sight for patients worldwide. Since debuting the world’s first disposable soft contact lens in 1987, it has been helping patients see better through their world-leading ACUVUE® Brand Contact Lenses. In 2017, J&J expanded into cataract surgery, laser refractive surgery (LASIK) and consumer eye health and now serves more than 60 million patients a day across 103 countries with its eye health portfolio. Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion

In-House Clinical Research Associate 
Location: Ettlingen
Full time employment contract for 12 months

The Clinical Research Associate provides administrative and organizational support for assigned clinical trials and sites. They are responsible for effectively managing multiple clinical study activities to assure accurate and timely initiation, enrollment, conduct and completion for assigned clinical trials.

Core Job Responsibilities

· Serving as internal support for all members of the assigned team

· Supporting investigative sites toward completion and appropriate submission of all required clinical trial documents prior to site initiation

· Supporting establishment and maintenance of the electronic Trial Master Files (eTMF) for assigned clinical trials

· Coordinating Institutional Review Board/ Ethics Committee (IRB/EC) approvals

· Supporting overall progress of clinical trials by regularly attending clinical trial team meetings, reviewing team communications and sharing pertinent information with assigned investigative sites, as requested 

· Assist the study team with study startup procedures, including preparing site binders.

· Assisting assigned clinical trial teams to ensure that each clinical trial maintains audit/inspection readiness at each site and internally throughout the duration of assigned clinical trials.

· Ensuring all equipment/supplies provided to investigative sites is appropriately tracked and reported 

  • BA/BS or equivalent years of experience required
  • 0-2 years of clinical research experience
  • Fluent in German and English 
  • Knowledge of ophthalmology highly desirable, but not required.
  • Ability to problem-solve.
  • Good communication via written, verbal and listening skills.
  • Ability to successfully manage multiple competing priorities and adapt quickly to changing priorities.
  • Proficiency with MS Word, Excel and PowerPoint

Primärer Standort
Deutschland-Baden Württemberg-Ettlingen-
AMO Germany GmbH (7137)
Clinical Research non-MD
Requisition ID