Recruiting Coordinator
SGS North America Inc.

Company Description

We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.

Job Description

This position is responsible for managing and developing study documents that are used on clinical trials. It is also responsible for creating, submitting, and closing out studies that are submitted to the IRB.

• Assists in the development of study documents and study preparation prior to the start of a study.
  
• Engages with CRCs (Clinical Research Coordinators) and study P.I.s during study preparation to ensure documents and procedures are documented in accordance with the protocol, GCP, and company SOPs.
  
• Manages the status and required items needed for studies involving the IRB, not limited to study submissions, deviation / SAE reporting, and study closeout.
  
• Engages with clients (when applicable) during study preparation phase to ensure all necessary documents (safety letter, informed consent, etc.) are finalized prior to IRB submission.
  
• Assists in the review and/or development of new protocols, assessments, procedures, and technologies.
  
• Assist with the development and updating of SOPs, WI, and training material related to study paperwork creation and IRB management.
  
• Ensure compliance with regulations.
  
• Provides excellent customer service to clients, and maintains positive interaction with peers and supervisors.
  
• Adheres to internal standards, policies, and procedures.
  
• Performs other duties as assigned.

• Bachelor's Degree, preferable in science or equivalent degree - Strongly Preferred
  
• Minimum 1 years of experience in clinical research or clinical recruiting - Required
  
• Research organization, and/or prior project management experience - Required
  
• Ability to coordinate multiple projects at once - Required
  
• Ability to work independently, use time wisely and multi-task - Required
  
• Previous IRB experience and / or clinical research regulatory experience - Preferred

• CCRC or CCRA Certification - Preferred

• Language Skills: English
• Mathematical Skills: Intermediate
• Reasoning Skills/Abilities: Intermediate
• Computer Skills: Proficiency with Microsoft Office applications, including Outlook, Word and Excel.
• Strong attention to detail and organizational and interpersonal skills