Site Management Associate I

PSI CRO AG; Çankaya; On-site; TRY 20,000 - 35,000; Full time

Job summary

A dynamic global company is seeking a candidate to support clinical research projects in Türkiye. The successful applicant will facilitate communication, handle documentation, and manage various project-related tasks, ensuring efficient operations. Proficiency in English and Turkish along with a life sciences degree is required. This hybrid role is based in Ankara, offering growth within a supportive environment focused on professional development.

Qualifications

• 1+ years of experience in Clinical Research / CRO environment.
• Full working proficiency in English and Turkish.
• Prior experience as a Site Coordinator is a plus.

Responsibilities

• Exchanges data and documents among project stakeholders.
• Maintains Trial Master File (TMF) and prepares study files.
• Ensures proper safety information flow with investigative sites.

Skills

Organizational skills

Problem-solving abilities

Customer service skills

Interpersonal skills

Detail-oriented

Multi-tasking abilities

Flexibility

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 Ankara

Job Description

Join our international team and be the key support to clinical research projects in Türkiye, 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 in Life Sciences
• 1+ years of experience in Clinical Research / CRO environment,preferably in an international setting
• Prior experience of work as a Site Coordinator is a plus
• Proficiency in standard MS Office applications
• Full working proficiency in English and Turkish
• 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.