Clinical Scientist

Ascendis Pharma

. Design clinical trials, provide oversight, and support site and subject retention .

Posted 10/3/2026full-timePrinceton • New Jersey • United StatesMid-LevelSenior💰 $160,000 - $180,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial design, oversight, and regulatory compliance, with a strong ability to analyze and interpret clinical data. Possesses advanced knowledge of good clinical practices and the ability to cultivate relationships with key stakeholders in the clinical research field.

Highest-signal resume keywords

Clinical Trial DesignRegulatory SubmissionsStatistical ConceptsExcellent Communication SkillsGood Clinical Practices

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProtocolsMonitoring PlansClinical Study ReportsData AnalysisDocument DraftingSafety and Efficacy Data TrackingInvestigator BrochuresSite Training MaterialsHealth Authority ResponsesRegulatory Guidance

Soft Skills

Problem SolvingCollaborationAttention to DetailTrustworthinessInitiative

Certifications & Qualifications

Advanced Degree (Ph.D., Pharm.D., MS)

Industry Keywords

Clinical ResearchEndocrine ProjectsEthical StandardsScientific MeetingsCross-Functional Teams

About the role

Key responsibilities & impact

Design clinical trials, provide oversight, and support site and subject retention
Ensure completion of clinical trial protocols, investigator brochures, monitoring plans, site training materials, clinical study reports, health authority responses, standard operating procedures, and related documents
Participate on study teams and cross-functional teams as delegated by the Vice President, Clinical Development
Ensure consistent use of language and criteria across multiple endocrine projects
Ensure study integrity and track accumulating safety and efficacy data
Anticipate clinical trial obstacles and implement solutions
Analyze, evaluate, and support accurate interpretation and reporting of clinical data
Draft and review clinical documents, manuscripts, presentations, and regulatory submissions
Maintain current knowledge of relevant science, medical information, good clinical practices, and regulatory guidance
Collaborate with cross-functional colleagues as a clinical research resource to optimize product development
Cultivate relationships with investigative sites, clinical consultants, and key opinion leaders
Support corporate strategic and organizational initiatives
Assist with commercial activities as needed
Complete assigned tasks thoroughly, accurately, and on time
Adhere to rigorous ethical standards
Travel up to 20% domestically and internationally for scientific meetings

Requirements

What you’ll need

Advanced degree e.g. Ph.D., Pharm.D., MS, or equivalent
Strong track record of scientific and clinical inquiry
Understand statistical concepts and clinical trial design
Understand the connection between nonclinical data and clinical data
Possess excellent communication skills (both written and verbal)
Learn quickly and follow complex directions under pressure
Multi-task while remaining organized and attentive to detail
Work hard and be a trustworthy and collaborative team player
Take initiative and solve problems of moderate complexity
Demonstrate sound judgement in handling complex, confidential, and regulated information
Lead both directly and by example

Benefits

Comp & perks

401(k) plan with company match
Medical, dental, and vision plans
Company-offered Life and Accidental Death & Dismemberment (AD&D) insurance
Company-provided short and long-term disability benefits
Unique offerings of Pet Insurance and Legal Insurance
Employee Assistance Program
Employee Discounts
Professional Development
Health Saving Account (HSA)
Flexible Spending Accounts
Various incentive compensation plans
Accident, Critical Illness, and Hospital Indemnity Insurance
Mental Health resources
Paid leave benefits for new parents
Discretionary annual bonus or incentive compensation plan eligibility
Discretionary stock-based long-term incentives
Paid time off
Comprehensive benefits package
Hybrid work arrangement from the Princeton, NJ office may be considered remote for the right candidate