Asuntos Regulatorios / CRA Position Available In Broward, Florida
Tallo's Job Summary: We are looking for a Regulatory Affairs / CRA to join a premier client in Sunrise, FL with a pay rate of $25 - $30/hr. Responsibilities include optimizing patient enrollment in clinical trials, managing trial materials, and ensuring timely data entry. Ideal candidates have a Bachelor's degree, experience in clinical research or regulatory affairs, organizational skills, and familiarity with GCP and ERP systems. Apply now for professional growth opportunities within a leading organization.
Job Description
Para aquellos que quieren seguir creciendo, aprendiendo y evolucionando. Nosotros en Kelly® ¡Te escucho, y estamos aquí para ti! We’re seeking a Regulatory Affairs / CRA to work at a premier client in Sunrise, FL. ¿Suena bien? Eche un vistazo más de cerca a continuación. You owe it to yourself to consider this great new opportunity.
Pay Rate :
$ 25 – $30 /hr Why you should apply to be a Regulatory Affairs /
CRA:
– Join a dynamic team committed to optimizing patient enrollment in clinical trials. – Work in a supportive environment that prioritizes adherence to industry standards and regulatory compliance. – Gain exposure to cutting-edge clinical practices and technologies. – Enjoy opportunities for professional growth and development within a leading organization. What’s a typical day as a Regulatory Affairs / CRA? You’ll be: – Ensuring procedures are in place for the appropriate optimization of patients into clinical trials, while monitoring the assigned trials according to company SOPs and GCP guidelines. – Planning and managing requirements for clinical trial materials, including ordering, monitoring expiration, and requesting extensions as necessary. – Tracking completed CRFs and establishing efficient systems for rapid data entry into databases, ensuring timely responses to queries generated during data cleaning. This job might be an outstanding fit if you: – Hold a Bachelor’s degree in a relevant field and have experience in clinical research or regulatory affairs, with a strong understanding of GCP and regulatory requirements. – Possess excellent organizational skills and the ability to manage multiple tasks, including inventory management and document archiving. – Are capable of conducting internal and external audits and have experience with ERP systems, specifically Exact ERP. What happens next Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. Pero no se preocupe, incluso si esta posición no funciona, todavía está en nuestra red. Eso significa que todos nuestros reclutadores tendrán acceso a su perfil, ampliando sus oportunidades aún más. Ayudarlo a descubrir lo que sigue en su carrera es nuestro objetivo, así que #x2019, manos a la obra.
