Site Management Associate I

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

Job summary

Join a forward-thinking company dedicated to improving lives through medical science. This hybrid role in Pretoria offers an exciting opportunity to support clinical research projects, ensuring effective communication and document management. With a focus on professional development, you will thrive in a dynamic environment that values teamwork and innovation. If you are detail-oriented and possess strong organizational skills, this is the perfect chance to advance your career while making a meaningful impact in the healthcare sector.

Qualifications

• Degree in Life Sciences required, with experience as Nurse or Pharmacist preferred.
• Prior administrative experience in Clinical Research or CRO environment is a plus.

Responsibilities

• Support clinical research projects by managing documents and maintaining systems.
• Coordinate communication between investigative sites and project teams.

Skills

Organizational Skills

Problem-Solving Abilities

Customer Service Skills

Interpersonal Skills

Detail-Oriented

Education

College/University Degree in Life Sciences

Tools

MS Office

Job 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

• Exchangesdata, documents and other project relevant information between investigative sites, site vendors and the project team
• Ensuresorder, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies
• Assistswith handling administrative financial tasks
• Coordinatespreparation for and follow-up on site, TMF and systems´ audits and inspections

Other Communication

• Exchangesdata, 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 administrativeexperience 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.