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Pfizer

Clinical Scientist

Pfizer

. Lead and manage execution of international and global observational and non-interventional studies .

Posted 10/8/2026full-timeBerlin • GermanyMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing international observational and non-interventional studies, with a strong focus on project management, stakeholder collaboration, and regulatory compliance. Proficient in coordinating cross-functional teams and driving evidence-generation strategies within the pharmaceutical or biotechnology sectors.

Highest-signal resume keywords
Clinical Research ManagementProject ManagementStakeholder ManagementGCP KnowledgeEpidemiology Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical ResearchObservational StudiesEpidemiologyData ReviewRegulatory SubmissionsStudy OperationsEvidence GenerationRisk IdentificationStudy PlanningMonitoring
Soft Skills
Communication SkillsCollaborationProblem SolvingLeadership
Industry Keywords
Life SciencesPublic HealthPharmacyMedicinePharmaceuticalBiotechnologyMigraineInfectious DiseasesObesityGlobal Study Teams

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Lead and manage execution of international and global observational and non-interventional studies
  • Drive operational execution and oversight of observational, epidemiological, pragmatic, and low-interventional studies
  • Partner with Medical Affairs, Statistics, Clinical Data Sciences, Regulatory, Safety, and external research teams
  • Manage studies governed by multiple global and local SOPs
  • Coordinate international study teams, vendors, and collaborators across regions and time zones
  • Lead study planning, execution, monitoring, data review, and reporting
  • Contribute to regulatory submissions, inspections, audits, publications, and scientific communications
  • Identify operational risks and develop solutions with stakeholders
  • Support continuous improvement and evidence-generation strategy development

Requirements

What you’ll need
  • Degree in Life Sciences, Public Health, Pharmacy, Medicine, or a related scientific field
  • Experience in clinical research, observational studies, epidemiology, or evidence generation
  • Experience working within multinational or global study teams
  • Strong project management and stakeholder management skills
  • Knowledge of clinical research processes, GCP, and study operations
  • Ability to work across multiple studies and functions simultaneously
  • Fluent English communication skills
  • Experience within pharmaceutical or biotechnology organizations preferred
  • Experience managing external vendors and research partners preferred
  • Therapeutic area experience in Migraine, Infectious Diseases, or Obesity is an advantage
  • Experience in global evidence-development programs preferred

Benefits

Comp & perks
  • Equal opportunity and non-discrimination throughout the recruitment process
  • Reasonable accommodations to support applications, interviews, and future careers
  • International, science-driven team environment
  • Opportunity to work on high-impact studies supporting patient care globally