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TFS HealthScience - Contract Research Organization

Clinical Scientist

TFS HealthScience - Contract Research Organization

Clinical Scientist providing scientific leadership and expertise in clinical development planning for innovative biotech company. Supporting study design, protocol development, and key milestones during growth phase.

Posted 8/3/2026contractCopenhagen • 🇩🇰 DenmarkMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in clinical development strategy, protocol development, and scientific communication within biotech and pharmaceutical environments. Capable of collaborating with cross-functional teams to drive clinical study design and strategic decision-making.

Highest-signal resume keywords
PhD, PharmD, MD, Or Advanced DegreeClinical DevelopmentClinical ResearchProtocol DevelopmentScientific Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Development PlanningTranslational ScienceClinical Study DesignStudy EndpointsTrial Design
Soft Skills
Scientific InsightsCollaborationStrategic Recommendations
Industry Keywords
BiotechPharmaceuticalCROTherapeutic Area

About the role

Key responsibilities & impact
  • Contribute to the development of the clinical strategy and clinical development plans for ongoing and future programs
  • Provide scientific input into clinical study concepts, protocol development, study endpoints, and overall trial design
  • Support preparation of clinical and scientific documentation for internal stakeholders, investors, regulatory interactions, and future study planning
  • Collaborate with cross-functional teams and external experts to evaluate scientific, clinical, and regulatory considerations impacting development programs
  • Monitor developments within the therapeutic area and provide scientific insights to support strategic decision-making

Requirements

What you’ll need
  • PhD, PharmD, MD, or other advanced degree in Life Sciences, Medicine, Pharmacy, or related scientific discipline
  • Strong experience within clinical development, clinical research, translational science, or clinical science roles within biotech, pharmaceutical, or CRO environments
  • Experience supporting clinical study design, protocol development, and clinical development planning
  • Strong scientific communication skills with the ability to translate complex clinical concepts into clear strategic recommendations
  • Experience from early-stage clinical development and biotech environments is highly desirable

Benefits

Comp & perks
  • Opportunities for personal and professional growth in a rewarding environment
  • Join a team that values collaboration, quality, and making a difference in the lives of patients