Global Site Budget & Contracts Manager (Remote)

Precision Medicine Group

Województwo mazowieckie

Remote

PLN 373,000 - 527,000

Full time

5 days ago
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Job summary

Precision Medicine Group is seeking a Site Contracts and Budget Manager to join our European team. This role is fully remote from Poland, Slovakia, Serbia, Romania, or Hungary.

You will develop global clinical trial budget templates, translate protocols into costed plans, and lead negotiations for site contracts and related agreements. Qualified candidates have 5+ years in clinical research, with hands-on experience creating site budgets for multi-country trials and familiarity with CTA budgets

Qualifications

  • Graduate, postgraduate, or 4-year college degree.
  • Experience in a CRO, pharmaceutical, biotechnology, or healthcare environment.
  • At least 5 years of relevant clinical research experience, including hands-on experience developing investigator/site budget templates.
  • Demonstrated experience developing global/multi-country budget templates for sponsor- or CRO-managed studies.

Responsibilities

  • Develop global/site budget templates from protocols and study docs.
  • Translate protocol requirements into detailed, scalable budgets with milestones.
  • Identify site-level costs including start-up, pharmacy, lab, imaging, archiving, overhead.
  • Review and negotiate site contracts, confidentiality agreements, and related documents.
  • Ensure budgets comply with CTA exhibits, payment terms, and study timelines.

Skills

Budget development
Contract review
Negotiation
Cross-functional teamwork
CTA knowledge

Education

Bachelor's degree

Tools

MS Office

Job description

Precision Medicine Group is seeking a Site Contracts and Budget Manager to join our European team. This role is fully remote from Poland, Slovakia, Serbia, Romania, or Hungary.

You will develop global clinical trial budget templates, translate protocols into costed plans, and lead negotiations for site contracts and related agreements. Qualified candidates have 5+ years in clinical research, with hands-on experience creating site budgets for multi-country trials and familiarity with CTA budgets

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