Site Management Associate I
Company: PSI CRO
Role summary
Site Management Associate I is a role at PSI CRO in Ankara, Ankara, Turkey (hybrid). Posted 2026-08-20. Experience level: 0-2. No degree required.
- Job title
- Site Management Associate I
- Company
- PSI CRO
- Location
- Ankara, Ankara, Turkey
- Work arrangement
- hybrid
- Category
- Healthcare Support
- Experience level
- 0-2
- Degree required
- No
- Date posted
- 2026-08-20
If you’re looking to jumpstart a career in clinical research, this is a fantastic entry-level opportunity that doesn't require a college degree. You’ll be gaining hands-on experience in a supportive, professional environment where you can build a stable foundation and grow your skillset within the global healthcare industry.
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, providing non-monitoring site management and administrative support, maintaining trial records and facilitating communication between investigative sites, vendors and project teams.
Site Management
Exchanges data, documents and other project-relevant information between investigative sites, site vendors and the project team
Serves as the main site contact for administrative and non-protocol related matters
Prepares regulatory and ethics committee submission/notification documents
Coordinates site payments and trial supplies
Supports site-specific query resolution and tracks EDC completion
Coordinates preparation for and follow-up on site audits and inspections
Other Communication
Exchanges information and documents with the project team and other departments
Organizes and participates in internal project team meetings
Assists with the organization of Investigator Meetings
Coordinates trial-related training for investigator sites
Document Management
Maintains Trial Master File (TMF) records and performs regular TMF checks
Prepares, distributes and updates Investigator Site Files (ISF) and ISF checklists
Coordinates translation of trial records
Provides support during TMF and systems audits
Vendor & Trial Management
Communicates with trial vendors and tracks vendor-related supplies
Tracks site issues and action items in CTMS
Ensures proper safety information flow with investigative sites
Other Assistance
Provides miscellaneous administrative project support, as applicable
Qualifications
College or university degree; relevant education, training and experience may also be considered
Experience in Clinical Research / CRO environment, preferably in an international setting, is a plus
Prior experience as a Site Coordinator is a plus
Proficiency in standard MS Office applications
Full working proficiency in English and Turkish
Good organizational, planning and problem-solving skills
Detail-oriented, flexible and able to work effectively in a fast-paced environment
Team-oriented with strong communication and interpersonal skills+
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.