Remote Senior Start-Up & Regulatory Lead

Precision for Medicine

Çankaya

Remote

TRY 450,000 - 700,000

Full time

48 hours ago
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Job summary

Precision Medicine Group is seeking a Senior Start Up & Regulatory Specialist to drive country level submissions and site activation in Turkey. You will coordinate regulatory activities, prepare submissions, and ensure timely authorizations for clinical trials.

Ideal candidates have 5+ years in regulatory/start-up roles within CRO or pharma, with fluency in English and Turkish and strong organizational skills. Remote work options in Turkey are available.

Qualifications

  • Requires a life sciences degree or nursing qualification with regulatory/start-up experience.
  • Minimum 5 years as Regulatory or Start-Up specialist in CRO/pharma settings.
  • Strong knowledge of regulatory submission processes and ICH-GCP principles.

Responsibilities

  • Lead country/site activation readiness and mitigate risks.
  • Coordinate activities for country-level regulatory submissions and site activations.
  • Prepare and submit Clinical Trial Applications and dossiers to authorities.
  • Maintain regulatory trackers and provide updates to leadership.

Skills

Fluent English
Fluent Turkish
Communication
Organizational skills

Education

Bachelors in Life Sciences
RN License

Tools

MS Office
Milestone tracking tools

Job description

Precision Medicine Group is seeking a Senior Start Up & Regulatory Specialist to drive country level submissions and site activation in Turkey. You will coordinate regulatory activities, prepare submissions, and ensure timely authorizations for clinical trials.

Ideal candidates have 5+ years in regulatory/start-up roles within CRO or pharma, with fluency in English and Turkish and strong organizational skills. Remote work options in Turkey are available.

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