Site Management Associate I

PSI CRO; Çankaya; Hybrid; TRY 25,000 - 45,000; Full time

Job summary

A leading company in clinical research is seeking support staff for projects based in Ankara. Ideal candidates will have a degree in Life Sciences and experience in a CRO environment. The role involves managing documentation, coordinating team meetings, and ensuring compliance with safety information flows.

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

• Manage communication and documentation for clinical research projects.
• Ensure inventory management of clinical supplies.
• Maintain Trial Master File and assist with audits.

Skills

Organizational skills

Problem-solving abilities

Flexibility

Interpersonal skills

Detail-oriented

Customer service

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 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.