Clinical Research Associate (CRA)

A Clinical Research Associate (CRA) job is available in Lake Worth, FL courtesy of Adecco Medical & Science.

CRA job’s primary responsible for supporting study management and data reports for clinical trials being conducted by the team. In addition, responsibilities include tracking and communicating the ongoing operation performance of each active study and study site.

Responsibilities:

Assists the clinical research team in all aspects of trial development and management.
Demonstrates ability to effectively communicate ideas and persuade others to accomplish goals and objectives.
Sets priorities consistent with company goals and focuses on high priority opportunities.
Takes steps to understand external customer and/or internal client needs and translate this knowledge into effective decisions.
Demonstrates principled leadership and sound business ethics; shows consistency among principles, values and behaviors
Encourages and supports information sharing and collaboration across departments.
Takes actions that are best for the company versus his or her individual unit.

Education/Experience Requirements:

Bachelor’s degree in the health, life sciences, or engineering.
Certification as a Certified Clinical Research Professional (CCRP) is preferred.
2-3 years minimum experience monitoring outcomes and randomized studies and, IDE study management/monitoring experience including facilitating approval review with Institutional Review Boards.
Travel up to 35% (Domestically)


If you are interested in this Clinical Research Associate job, please APPLY NOW.

Equal Opportunity Employer Minorities/Women/Veterans/Disabled

  • Apply with Adecco

Reference number US_EN_2_106405_332610