Site Management Associate I

PSI CRO AG; Pretoria; On-site; ZAR 30 000 - 60 000; Full time

Job summary

Join a dynamic global company dedicated to improving lives through medical science. As a key support member for clinical research projects, you will streamline communication, maintain essential systems, and manage critical documents. This role offers a unique opportunity to work in a hybrid environment, balancing remote and on-site responsibilities. The company values its employees, providing ample opportunities for professional development and growth. If you are detail-oriented, organized, and possess strong interpersonal skills, this position is perfect for you. Embrace the chance to make a significant impact in the field of clinical research.

Qualifications

• Degree in Life Sciences required; Nurse or Pharmacist experience preferred.
• Prior administrative experience in Clinical Research is a plus.

Responsibilities

• Support clinical research projects by managing documents and communication.
• Maintain Trial Master File and assist with audits and inspections.

Skills

Organizational Skills

Problem-Solving Abilities

Interpersonal Skills

Detail-Oriented

Flexibility

Education

College/University Degree in Life Sciences

Tools

MS Office

Job description

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

This role is hybrid - Based in Pretoria

Job Description

Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.

Site Management

• Exchanges data, documents and other project relevant information between investigative sites, site vendors and the project team
• Ensures order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies
• Assists with handling administrative financial tasks
• Coordinates preparation for and follow-up on site, TMF and systems´ audits and inspections
  
  
  

Other Communication

• Exchanges data, documents, and other information with the project team and other departments
• Provides assistance with organization of internal team meetings
• Prepares draft minutes of internal team meetings
• Assists with preparation, attendance and follow-up of Investigator’s Meetings, as applicable
• Under supervision, maintains study-specific and corporate tracking systems
  
  
  

Document Management

• Maintains Trial Master File (TMF)
• Perform TMF review and oversight at country and site level
• Prepares, distributes, and updates Onsite Study Files (OSF) and OSF checklists
• Provides assistance with translations
  
  
  

Safety Management

• Ensures proper safety information flow with investigative sites
  
  
  

Other Assistance

• Provides miscellaneous administrative project support (if applicable)
  
  
  

Qualifications

• College/University Degree (Life Sciences)
• Prior experience of work as Nurse or Pharmacist
• Prior administrative experience in Clinical Research / CRO environment, preferably in an international setting, is a plus
• Proficiency in standard MS Office applications
• Good organizational and planning skills, problem-solving abilities, flexibility
• Detail-oriented, able to multi-task and work effectively in a fast-paced environment
• Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects
  
  
  

Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.