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Clinical Scientist in Late Phase - Sponsor dedicated - Home Based in UK or Spain or Poland or R[...]
  • Warsaw
Clinical Scientist in Late Phase - Sponsor dedicated - Home Based in UK or Spain or Poland or R[...]
Warszawa, Warsaw, Masovian Voivodeship, Polska
Syneos Health
13. 12. 2025
Informacje o stanowisku

Clinical Scientist in Late Phase – Sponsor dedicated – Home Based (UK, Spain, Poland, Romania, Bulgaria)

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Job Responsibilities

  • Work as a Clinical Scientist in Late Phase for a top pharma, focusing on oncology and vaccine studies.
  • Provide observational study execution, including epidemiological, non-interventional, pragmatic and low-interventional studies.
  • Manage study execution, monitoring, analysis, reporting and oversight of core team activities within one or more asset programs.
  • Collaborate with cross‑functional colleagues and oversee vendors to execute studies.
  • Act as co‑lead of the Study Core Team, executing studies within a matrix organization.
  • Support complex or low‑complexity studies across SOPs, including protocol training, vendor management, study planning, data review, regulatory documentation and publication preparation.
  • Work in a global environment on studies across all regions including International, Emerging Markets and China.
  • Identify issues promptly, lead implementation of solutions, and escalates as appropriate.

Qualifications

  • BA/BS in life sciences or health‑related field with 5+ years practical experience or MS/MBA with 3+ years, PharmD/PhD with 2 years, MD/DO with 1 year.
  • Industry experience in a Clinical Scientist role or similar capacity.
  • Experience with multinational teams/studies.
  • Hands‑on experience in epidemiology study design, conduct and analysis.
  • Experience leading study teams and working collaboratively with multiple functional groups.
  • Strong knowledge of GCP, monitoring, clinical and regulatory operations.
  • Demonstrated independent authorship of study protocols and other documents.
  • Working knowledge of statistics, data analysis and interpretation.
  • Experience managing external vendors for clinical or epidemiological studies.
  • Fluent in English (writing, reading, speaking) with exceptional written and oral communication skills.

Benefits

  • Competitive remuneration package with excellent benefits.
  • Commitment to your development and training with career progression opportunities.
  • Opportunity to work in a successful and rewarding environment.

Seniority level

Mid‑Senior level

Employment type

Full‑time

Job function

Research, Analyst, and Information Technology

If you are interested in this role and believe you would be the right fit, we would be more than happy to hear from you. Apply online.

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