Clinical Research Associate

4 weeks ago

Dallas, United States Astrix Full time

Exciting 2 year CRA development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world – with complementary businesses in Surgical and Vision Care.


Clilnical Research Associate

  • Monitor and manage clinical trials, at the sites under your responsibility, related to eye diseases, ophthalmic treatments, and ophthalmic devices.
  • Ensure that these trials are conducted in compliance with international guidelines, local regulations, industry standards, and study protocols.
  • Regionally based and involves working with multiple clinical trial sites across multiple protocols. Must be in NC, FL, SC, GA or TX Remote


Site Selection and Initiation, Monitoring and Site Management, Regulatory Compliance, Investigational Product (IP) and Clinical Supplies Oversight, Data Management, Safety Reporting, Close-Out Visits, Documentation and Reporting


Qualifications:

• Bachelor's degree in a related field (life sciences, nursing, etc.).

• Previous experience as a Clinical Research Associate, in ophthalmology

• Knowledge of ophthalmic diseases, treatments, and related medical terminology, including ophthalmic devices.

• Strong understanding of clinical research regulations and Good Clinical Practice (GCP) guidelines.

• Excellent communication and interpersonal skills.

• Attention to detail and the ability to work independently and as part of a team.

• Willingness to travel as needed for on-site monitoring visits.

• Certification as a Certified Clinical Research Associate / Professional (CCRA / CCRP) or similar credential is a plus.


This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you

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