Affaires réglementaires / ARC Position Available In Broward, Florida

Tallo's Job Summary: Join a dynamic team in Sunrise, FL as a Regulatory Affairs / CRA, with a pay rate of $25 - $30/hr. Responsibilities include optimizing patient enrollment in clinical trials, managing trial materials, and ensuring efficient data entry. Ideal candidates have a Bachelor's degree, experience in clinical research or regulatory affairs, and strong organizational skills. Apply now for professional growth and development opportunities within a leading organization.

Company:
Kelly Services
Salary:
$62400
JobFull-timeOnsite

Job Description

Pour ceux qui veulent continuer à grandir, apprendre et évoluer. Chez Kelly® écoutez-vous, et nous sommes là pour vous ! We’re seeking a Regulatory Affairs / CRA to work at a premier client in Sunrise, FL. Bon son? Regardez de plus près ci-dessous. 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. Mais ne vous inquiétez pas, même si ce poste ne fonctionne pas, vous êtes toujours dans notre réseau. Cela signifie que tous nos recruteurs auront accès à votre profil, ce qui élargira encore plus vos opportunités. Vous aider à découvrir la suite de votre carrière est notre raison d’être, alors laissez-nous& #x2019;s se mettent au travail.

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