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Clinical Trial Associate

JobsInMass.com

Morocco, Indiana, United States • Vollzeit

Bewerben Sie sich als Erste/r!

Erfahrung
Beliebig
Gehalt
Stellenangebote
1
Veröffentlicht
vor 3 Stunden
Arbeitsmodus
Im Büro
Ausbildung
BS or MS in science, engineering, or technical discipline
Wieder aufnehmen
Bewerbung erforderlich

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Stellenbeschreibung

About BioSensics

BioSensics is a leading biomedical engineering company focused on developing wearable medical sensors and telehealth devices. Our products aid physiological monitoring, telehealth services, and biofeedback in sectors such as elderly care, physical therapy, rehabilitation, orthopedics, and neurology.

Position Overview

We seek a motivated, detail-focused, and proactive Clinical Trial Associate to join our expanding team. This role involves independently overseeing all operational elements of clinical trial projects. Serving as the primary liaison to the study sponsor, you will ensure that project deadlines and BioSensics deliverables are consistently achieved for assigned clinical studies.

Key Responsibilities

  • Provide administrative assistance to the Clinical Operations Department.
  • Assist the Clinical Operations team in actively managing clinical studies.
  • Organize and track study equipment and materials efficiently.
  • Review and monitor study data to oversee device performance in the field.
  • Deliver customer and technical support to clinical sites and participants.
  • Attend both internal and external meetings and prepare detailed minutes.
  • Support maintenance, quality control, and archiving of clinical documentation.
  • Manage and coordinate both internal and grant-funded clinical study operations.
  • Develop a comprehensive understanding of BioSensics products.
  • Adhere strictly to established procedures and contribute suggestions to enhance operational effectiveness and accuracy.

Desired Skills and Qualifications

  • Exceptional organizational skills and attention to detail.
  • Experience handling Protected Health Information (PHI) with knowledge of HIPAA compliance.
  • Ability to juggle multiple priorities and tasks effectively.
  • Previous experience engaging with clinical study participants is advantageous.
  • Capable of working both independently and collaboratively within a team.
  • Strong verbal and written communication capabilities.
  • Bachelor’s or Master’s degree in science, engineering, or a related technical field.

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