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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 We've kept it here for historical reference.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!

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Principal Regulatory and Start Up Specialist

Job Overview

Location

Remote, Turkey

Job Type

Full-time

Category

HR & Recruiting

Date Posted

April 14, 2026

Full Job Description

đź“‹ Description

  • • The Principal Regulatory and Start Up Specialist plays a critical role in ensuring timely and compliant site activation for clinical trials, directly supporting Precision for Medicine’s mission to advance precision medicine in rare diseases, oncology, and other therapeutic areas by managing regulatory submissions and site readiness across assigned countries.
  • • Day to day responsibilities include preparing and submitting Clinical Trial Application Forms and dossiers to Competent Authorities and Ethics Committees, coordinating country-level submissions, maintaining project trackers and regulatory intelligence tools, customizing informed consent documents, managing essential document collection for site activation, liaising with site CRAs, and providing regular updates to regulatory leads and project teams.
  • • The role operates within Precision for Medicine, a Clinical Research Organization specializing in integrated precision medicine solutions, combining innovative trial design, biomarker analytics, medical expertise, and a deep commitment to rare disease and oncology research, with a growing global team focused on quality and compliance.
  • • The specialist will deepen expertise in international and local clinical trial regulations (ICH-GCP), lead mentoring of junior staff, drive process improvements, gain experience in cross-functional coordination across Clinical Operations, Project Management, and Site Contracts, and develop leadership capabilities by potentially acting as Start Up Lead on smaller or regional studies.

🎯 Requirements

  • • Bachelor’s degree in life sciences or related field, or Registered Nurse (RN) or equivalent combination of education, training, and experience
  • • 5+ years of experience as a Regulatory or Start Up Specialist in a CRO, pharmaceutical, or biotech environment
  • • Fluency in both English and Turkish

🏖️ Benefits

  • • Opportunity to mentor junior staff and share expertise in local country regulations and internal procedures
  • • Involvement in departmental process improvement initiatives, including ownership, rollout, and periodic reviews
  • • Potential to act as Start Up Lead on smaller or regional studies, driving site activation timelines under global leadership direction

Skills & Technologies

GCP
Senior
Remote
Degree Required

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About PFM Asset Management

PFM Asset Management is a distinguished investment management firm specializing in providing tailored investment solutions for institutional clients. With a strong focus on fiduciary responsibility and long-term value creation, PFM offers a comprehensive range of services including fixed income, equity, and alternative investment strategies. Their approach is grounded in rigorous research, disciplined risk management, and a deep understanding of client objectives. PFM is committed to transparency and client service, striving to be a trusted partner in helping institutions achieve their financial goals. They serve a diverse clientele, including public funds, corporate pensions, endowments, and foundations, adapting their strategies to meet unique needs.

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