The Sr. Clinical Trial Manager is responsible for effective conduct of Ascendis’ global and regional clinical trials, contributing to the company’s focus on making a meaningful difference in patients’ lives.
Requirements
- Bachelor’s degree or master’s degree in natural or health sciences (biology, pharmacology, pharmaceutical sciences or equivalent)
- 7+ years of combined experience in managing/monitoring Phase 1, 2, or 3 clinical trials.
- High proficiency in English with strong communication and presentation skills
- Experience managing and overseeing vendors
- Experience in performing clinical site monitoring visits, including remote visits
- Ability to prioritize and to work independently on assigned tasks, manage timelines, and to present ideas to sites / stakeholders clearly and effectively
- High proficiency with Veeva Systems (Clinical Vault eTMF, Veeva EDC), CTMS, Endpoint IRT and Microsoft Office (Outlook, Word, Excel, PowerPoint)
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
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