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This position was posted on April 14, 2026 and is likely no longer accepting applications. We've kept it here for historical reference. Check out the similar jobs below!
Job Overview
Location
Remote, Turkey
Job Type
Full-time
Category
HR & Recruiting
Date Posted
April 14, 2026
Full Job Description
đź“‹ Description
- • As a Principal Regulatory and Start Up Specialist at Precision Medicine Group, you will play a critical role in ensuring the timely and high-quality activation of clinical trial sites across assigned countries, directly contributing to the advancement of precision medicine in oncology and rare diseases.
- • Day to day, you will drive country-level submissions and site activation processes, prepare and manage Clinical Trial Application Forms and submission dossiers for Competent Authorities and Ethics Committees, maintain project plans and regulatory intelligence tools, coordinate with cross-functional teams including Clinical Operations and Project Management, and mentor junior staff on local regulations and internal procedures.
- • Precision Medicine Group is a Clinical Research Organization dedicated to advancing precision medicine through integrated clinical trial design, biomarker analytics, and deep expertise in rare diseases and oncology, with a mission to improve patient outcomes through science-driven innovation.
- • In this role, you will deepen your expertise in global regulatory affairs, lead site start-up initiatives, influence cross-functional collaboration, and contribute to process improvements that enhance efficiency and compliance across international clinical trials.
🎯 Requirements
- • Bachelor’s degree in life sciences or related field, or Registered Nurse (RN) with equivalent education and experience
- • 5+ years of experience as a Regulatory or Site Start-Up Specialist in a CRO, pharmaceutical, or biotech environment
- • Fluency in both English and Turkish
- • Excellent communication, organizational, and computer skills
- • Ability to prioritize workload, meet deadlines, and drive cross-functional coordination
- • Experience with milestone tracking tools and regulatory submission processes (CA/EC/IRB)
🏖️ Benefits
- • Opportunity to work remotely from Turkey with a global Clinical Research Organization
- • Impactful role in advancing cancer and rare disease therapies through precision medicine
- • Professional growth through mentoring junior staff and leading process improvement initiatives
- • Exposure to international regulatory frameworks and cross-functional project leadership
- • Support for continuous learning and development in a mission-driven, inclusive workplace
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About Precision Medicine Group
Precision Medicine Group (PMG) is a leading life sciences consulting firm dedicated to accelerating the development and commercialization of precision medicine. They offer a comprehensive suite of services, including strategy, market access, regulatory affairs, and commercialization support. PMG partners with pharmaceutical, biotechnology, and diagnostic companies to navigate the complex landscape of personalized healthcare. Their expertise spans various therapeutic areas and advanced molecular technologies. By leveraging deep scientific knowledge and market insights, PMG helps clients optimize their drug development pipelines, secure regulatory approvals, and successfully launch innovative therapies. They are committed to advancing patient care through the power of precision medicine, ensuring that the right treatments reach the right patients at the right time.
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