Site Identification Specialist (Feasibility)

PSI CRO AG; Çankaya; On-site; TRY 1,220,000 - 1,831,000; Full time

Job summary

PSI CRO AG is seeking a Site Identification Specialist to develop strategic relationships with clinical research sites and enhance clinical trial progress. The role involves project management, site coordination, and maintaining compliance with local regulations. Candidates should hold a relevant degree and possess experience in on-site monitoring with proficiency in Turkish and English.

Benefits

Flexible working conditions

Extensive training and a supportive team

Competitive salary and benefits

Qualifications

• At least 3 years of proven experience in on-site monitoring activities.
• Proficiency in Turkish and English.
• Understanding of Good Clinical Practice and local laws in Turkey.

Responsibilities

• Maintain and refine internal site databases with various teams.
• Define study objectives and create a potential site list.
• Evaluate status and progress of site identification.

Skills

Communication

Collaboration

Compliance with regulations

Education

University/College degree in Life Sciences, Pharmacy, Healthcare

Job description

Site Identification Specialist (Feasibility)

• Full-time

We are the company that cares – for our staff, clients, partners, and the quality of our work. Founded in 1995, we are a dynamic, global company with 3,000 dedicated individuals working at the forefront of medical science to bring new medicines to those in need.

We are seeking an experienced professional to develop strategic relationships with clinical research sites, aiming to optimize and advance clinical trial progress.

General Responsibilities:

• Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations, and Process Improvement teams.
• Participate in developing improvement strategies for site identification, implement them, and conduct related training activities.

Project Responsibilities:

• Define main study objectives and the optimal site profile.
• Create an initial list of potential sites.
• Coordinate with project teams at the project/regional level to refine strategies and methodologies for initial and follow-up site contacts, considering indication, regional specifics, and technologies.
• Maintain a study site identification tracker for evaluation and selection activities.
• Evaluate the status and progress of site identification, and identify potential risks or issues affecting timelines or objectives.
• Perform due diligence checks on regulatory and legal limitations with Legal, for investigators or sites.
• Support the project team throughout study startup and additional site identification rounds, providing necessary information about sites/investigators.

Minimum Qualifications:

• University/college degree in Life Sciences, Pharmacy, Healthcare, or equivalent experience.
• At least 3 years of proven experience in on-site monitoring activities.
• Proficiency in Turkish and English.
• Understanding of Good Clinical Practice, local laws, and regulations in Turkey.
• Strong communication and collaboration skills.
• Ability to work in a dynamic environment under tight deadlines across multiple projects.

We Offer:

• Flexible working conditions.
• Extensive training and a supportive team.
• Competitive salary and benefits.

Take your career to the next level. Join a company committed to employee well-being and professional growth.