Senior Clinical Scientist
Ascendis Pharma
full-time
Posted on:
Location Type: Hybrid
Location: Palo Alto • California • 🇺🇸 United States
Visit company websiteSalary
💰 $170,000 - $190,000 per year
Job Level
Senior
About the role
- 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
Requirements
- 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
- Preferred, but not required:
- 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
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical trial designclinical trial protocolsmonitoring plansclinical study reportsregulatory submissionsstatistical conceptsgood clinical practicesdata analysissafety and efficacy data trackingscientific inquiry
Soft skills
communication skillsorganizational skillsproblem-solvingattention to detailcollaborationinitiativetrustworthinessleadershipadaptabilityjudgment
Certifications
Ph.D.Pharm.D.MS