Senior Clinical Scientist - Job ID: SCS
Senior Clinical Scientist - Job ID: SCS
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Salary Not Disclosed
1 Vacancy
Job Description
Ascendis Pharma is a dynamic fast-growing global biopharmaceutical company with locations in Denmark Europe and the United States. Today were advancing programs in Endocrinology Rare Disease and Oncology.
Here at Ascendis we pride ourselves on exceptional science visionary leadership and skilled and passionate colleagues.
Guided by our core values of Patients Science and Passion we use our TransCon drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.
Our culture fosters a place where skilled adaptable and highly resourceful professionals can truly make their mark. We offer a dynamic workplace for employees to grow and develop their skills.
The Senior Clinical Scientist is involved in the design monitoring and data analysis of the Companys late-phase clinical trials studying growth hormone parathyroid hormone and/or C-type natriuretic peptide therapies. As such the Senior Clinical Scientist is an important and visible member of the Clinical Development team. The Senior Clinical Scientist position is based in the United States ideally the Scientist will work hybrid from our Palo Alto CA office but we may consider a remote arrangement for the right candidate.
Key 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 withand serve as a clinical research resource forcross-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
Estimated compensation 170-190K/year USD DOE
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
A note to recruiters:
We do not allow external search party solicitation. Presentation of candidates without written permission from the Ascendis Pharma Inc. Human Resources team (specifically from: Talent Acquisition Partner or Human Resources Director) is not this occurs your ownership of these candidates will not be acknowledged.
Required Experience:
Senior IC
Employment Type
Full-Time
