Site Identification Specialist (Feasibility)

PSI CRO; Çankaya; On-site; TRY 60,000 - 80,000; Full time

Job summary

A leading global company in medical science is seeking an experienced professional to develop strategic relationships with clinical research sites. The role involves optimizing clinical trials, managing site databases, and evaluating project progress, requiring a degree in Life Sciences and full proficiency in Turkish and English.

Benefits

Excellent and flexible working conditions

Extensive training and supportive team

Competitive salary and benefits package

Qualifications

• Minimum of 3 years proven experience in on-site monitoring activities.
• Full professional proficiency in Turkish and English.
• Understanding of Good Clinical Practice and local regulations.

Responsibilities

• Maintain internal site databases with various teams.
• Communicate strategy and methodology with project teams.
• Work with Legal for due diligence checks.

Skills

Communication

Collaboration

Flexibility

Education

University/college degree in Life Sciences, Pharmacy, Healthcare or equivalent

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 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.

Job Description

We are seeking an experienced professional dedicated to developing strategic relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials.

General Responsibilities:

• Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations, and Process Improvement teams.
• Participate in the development of improvement strategies for the site identification process, 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.
• Communicate with project teams at the project/regional level to fine-tune strategy and methodology for initial and follow-up site contacts, considering indication, regional specifics, and technologies in use.
• Maintain a study site identification tracker in collaboration with the project team for further site evaluation and selection.
• Liaise with project teams to evaluate the status and progress of site identification, and identify potential risks or issues affecting timelines or objectives.
• Work with Legal to perform due diligence checks on regulatory and legal limitations applicable to investigators or clinical sites.
• Support the project team throughout study startup and subsequent phases, especially when additional site identification rounds or information are needed.

Qualifications:

• University/college degree in Life Sciences, Pharmacy, Healthcare, or an equivalent combination of education, training, and experience.
• Minimum of 3 years proven experience in on-site monitoring activities.
• Full professional proficiency in Turkish and English.
• Understanding of Good Clinical Practice, local laws, and applicable regulations in Turkey.
• Strong communication and collaboration skills.
• Ability to work in a dynamic environment under tight deadlines across multiple projects with unique requirements.

Additional Information

• Excellent, flexible working conditions.
• Extensive training and a supportive team.
• Competitive salary and benefits package.

Take your career to a new level. Join a company committed to prioritizing its employees and investing in their ongoing professional growth and success.