Senior Start-Up & Regulatory Specialist (Remote Turkey)

Precision Medicine Group; Çankaya; Remote; TRY 900,000 - 1,400,000; Full time

Job summary

Precision Medicine Group is seeking a (Senior) Start Up & Regulatory Specialist to drive site activation readiness in Turkey and coordinate country-level submissions. The role ensures timely approvals, manages essential documents, and collaborates with cross-functional teams to navigate regulatory requirements in oncology and rare diseases.

Ideal candidates have 5+ years in regulatory/start-up roles within CRO or pharma, with fluency in English and Turkish, and the ability to work remotely in

Qualifications

• Bachelor's degree in life sciences or nursing required.
• Experience in regulatory/start-up roles in CRO/pharma preferred.
• Fluency in English and Turkish; strong communication skills.

Responsibilities

• Lead country/site activation readiness and mitigate risks.
• Coordinate country-level regulatory submissions and start-up activities.
• Prepare and submit Clinical Trial Applications and dossiers to authorities.
• Maintain project plans, trackers, and regulatory intelligence tools.
• Collaborate with site CRAs and internal teams to ensure activation timelines.

Skills

Excellent communication

Organizational skills

Fluency in English

Fluency in Turkish

Cross-functional leadership

Prioritize workload

Education

Bachelor's degree in life sciences

Registered Nurse (RN)

Advanced degree in life sciences

Job description

Precision Medicine Group is seeking a (Senior) Start Up & Regulatory Specialist to drive site activation readiness in Turkey and coordinate country-level submissions. The role ensures timely approvals, manages essential documents, and collaborates with cross-functional teams to navigate regulatory requirements in oncology and rare diseases.

Ideal candidates have 5+ years in regulatory/start-up roles within CRO or pharma, with fluency in English and Turkish, and the ability to work remotely in