Note: The job is a remote job and is open to candidates in USA. Ascendis Pharma is a global biopharmaceutical company developing therapies in endocrinology, rare disease, and oncology using its TransCon® drug development platform. The Clinical Scientist supports the design, oversight, monitoring, and analysis of late-phase clinical trials, while contributing to clinical documents, regulatory submissions, cross-functional collaboration, and product development initiatives.

Responsibilities

• For clinical trials: design, provide oversight, and support site and subject retention
• Ensure successful completion of documents (including clinical trial protocols, investigator brochures, monitoring plans, site training materials, clinical study reports, health authority responses, standard operating procedures, etc.) with cross-functional team members
• Participate on study teams and cross-functional teams as appropriate, and 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 obstacles within a clinical trial, and implement solutions
• Analyze, evaluate, and support accurate interpretation and reporting of clinical data
• Contribute to drafting and reviewing clinical documents, manuscripts, presentations, and regulatory submissions
• Maintain up-to-date knowledge of relevant science, medical information, good clinical practices, and regulatory guidance
• Collaborate with—and serve as a clinical research resource for—cross-functional colleagues to optimize product development
• Cultivate relationships with investigative sites, clinical consultants, and key opinion leaders to represent the interests of the company
• 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

Skills

• 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, follow complex directions under pressure
• Multi-task while remaining organized and attentive to detail
• Work hard, be a trustworthy and collaborative team player
• Take initiative and solve problems of moderate complexity
• Demonstrate sound judgement in terms of handling complex, confidential, and regulated information
• Lead both directly and by example
• At least 4 years of experience with clinical trial design and execution
• At least 4 years of pharmaceutical industry experience
• Experience with regulatory submissions and interactions

Benefits

• 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 an incentive compensation plan (eligibility varies based on role and position level)
• Discretionary stock-based long-term incentives
• Paid time off
• Hybrid work from the Princeton, NJ office, with a remote arrangement considered for the right candidate

Company Overview

Company H1B Sponsorship