Selected: đ Compliance.
Selected: đ”đ± Poland â Remote.
Selected: đ Date Added.
đ„ 1 hour ago
Senior Regulatory Affairs Manager overseeing regulatory strategy and delivery at ICON, a global healthcare intelligence and clinical research organization. Coaching teams and advising clients across drug development.
đ„ 4 hours ago
Regulatory and Start Up Specialist supporting clinical-trial submissions and site activation. Precision for Medicineâs CRO operations advance precision-medicine research.
đ Poland, Hungary â Remote
đ° $75M Private Equity Round on 2015-12
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 10%
đŁïžđđș Hungarian Required
đ„ 4 hours ago
Regulatory specialist supporting Hungarian clinical-trial submissions and site activation. Coordinating authorities, essential documents, translations, and cross-functional start-up activities for a precision-medicine CRO.
đ Poland, Hungary â Remote
đ° $35.2M Venture Round on 2021-03
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 23%
đŁïžđđș Hungarian Required
đ 2 days ago
Advanced Regulatory Affairs Associate supporting 3Mâs safety, environmental, and regulatory compliance. Ensuring product responsibility for materials, products, and technologies.
đ”đ± Poland â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ Compliance
đ«đšâđ No degree required
đ» Ghost score 10%
đ 2 days ago
Clinical Compliance Manager supporting GCP quality and regulatory compliance for Parexelâs clinical studies. Managing risk, CAPAs, vendors, and inspection readiness remotely from Spain or Poland.
đ Spain, Poland â Remote
đ° Venture Round on 1990-01
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 10%
đ 6 days ago
Compliance analyst investigating AML, fraud, and suspicious activity for MoneyGram. Reviewing cases, filing Suspicious Activity Reports, and supporting global regulatory risk mitigation.
đ”đ± Poland â Remote
đ° Corporate round on 2023-09
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 10%
đ 6 days ago
General Manager owning GoMiningâs crypto custody, compliance, money movement, and engineering operations. Driving KYC/AML, fraud controls, provider partnerships, product strategy, and team delivery.
đ Cyprus, Georgia, +4 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 15%
đ September 23
Vendor quality and compliance manager overseeing clinical research suppliers, audits, CAPAs, and risk management at Parexel. Supporting Medical Affairs and Research Collaboration compliance across Poland.
đ”đ± Poland â Remote
đ° Venture Round on 1990-01
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 10%
đ September 22
Study Start-Up and Regulatory Affairs Specialist supporting rare disease and oncology clinical trials at Ergomed, a specialist CRO. Coordinating regulatory submissions, site agreements, and initiation readiness across countries.
đ New Zealand, Poland â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ Compliance
đ» Ghost score 19%
đ September 21
Regulatory Manager guiding clinical-trial strategy and submissions for Precision for Medicine, a life-sciences CRO. Coordinating regulatory authorities, ethics committees, project teams, and submission specialists.
đ”đ± Poland â Remote
đ” zĆ190.2k - zĆ285.4k / year
đ° $75M Private Equity Round on 2015-12
â° Full Time
đ Senior
đ Compliance
đ» Ghost score 0%
đ September 21
Regulatory Manager guiding clinical-trial strategy and submissions for Precisionâs oncology and rare-disease CRO. Coordinating regulatory documents, authorities, ethics committees, and global project teams.
đ”đ± Poland â Remote
đ” zĆ190.2k - zĆ285.4k / year
đ° $35.2M Venture Round on 2021-03
â° Full Time
đ Senior
đ Compliance
đ» Ghost score 13%
đ September 21
Regulatory Affairs Manager guiding clinical-trial submissions and approvals across EMEA, Asia Pacific, and Latin America. Supporting CRO business development, compliance, and junior staff development.
đ Romania, France, +5 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 10%
đ September 18
Regulatory Affairs Consultant managing post-approval CMC submissions for biological and plasma products at Parexel. Conducting global change-control assessments and coordinating regulatory documentation across Europe.
đ United Kingdom, Croatia, +5 more countries â Remote
đ° Venture Round on 1990-01
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đŹđ§ UK Skilled Worker Visa Sponsor
đ» Ghost score 10%
đ September 18
Regulatory Affairs Consultant managing post-approval CMC submissions for Parexel's clinical development and regulatory services. Supporting vaccine and biological-product compliance across European locations.
đ Italy, Croatia, +5 more countries â Remote
đ° Venture Round on 1990-01
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 10%
đ September 18
GRC Lead managing security risk, controls, and ISO 27001 governance for Salmonâs Southeast Asian banking and lending platform. Advising governance forums and driving remediation across a regulated technology group.
đ September 16
GRC Specialist building compliance frameworks and customer audits for Secfix, which automates security compliance across Europe. Owning platform content and framework implementation.
đ Germany, United Kingdom, +3 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 25%
đŁïžđ©đȘ German Required
đ September 16
GRC Specialist building compliance frameworks and leading customer audits for Secfix, a European security compliance automation platform. Owning platform content and partnering with product, engineering, and customers.
đ United Kingdom, Germany, +3 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 25%
đ September 9
Senior Director leading quality and compliance strategy for Worldwide Clinical Trials, a global CRO. Overseeing clinical research quality governance, inspections, CAPA, regulatory compliance, and global teams.
đ September 4
Application Security specialist auditing CVE tasks for Meridialâs AI training systems. Evaluating vulnerabilities, exploits, mitigations, and technical accuracy.
đ Anywhere in the World
đ” $70 - $100 / hour
đ„ Funding within the last year
đ° $100M Series unknown on 2025-10
âł Contract/Temporary
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 0%
đ August 31
Regulatory submission manager leading CTIS and Veeva clinical-trial submissions for ICON, a global healthcare intelligence and clinical research organization. Coordinating regulatory documents, translations, approvals, and study-team delivery.
đ Poland, Romania, +2 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 16%
+14 More Compliance Jobs Available!
The average salary for remote compliance in Poland is PLNÂ 718,060 per year. This is based on data from 101 job openings. Our advanced AI searches the internet for remote job openings and posts them on our website. We use the salary data from these job postings to calculate salary expectations.
Below is a breakdown of salary data by years of experience:
| Experience | Number of roles analyzed | Average Salary |
|---|---|---|
âȘïž Entry-level Compliance (0 yrs) | 1 | PLNÂ 0 |
đą Junior Compliance (1-2 yrs) | 18 | PLNÂ 538,232 |
đĄ Mid-level Compliance (2-4 yrs) | 43 | PLN 726,011 |
đ Senior Compliance (5-9 yrs) | 35 | PLNÂ 903,355 |
đŽ Lead Compliance (10+ yrs) | 4 | PLN 0 |
We analyzed 80 job listings in the last year and found it takes about 35 days for employers to close a job opening.
We reviewed 101 job postings and found the top 10 skills employers are asking for most often are:
We scan the internet everyday and find jobs not posted on LinkedIn or other job boards.
We find jobs minutes after they're posted, so you can apply before everyone else.
Most members hear back within the first week
We find jobs other job boards miss.