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Ascendis Pharma
Ascendis Pharma
501 – 1,000 कर्मचारी
H1B वीज़ा प्रायोजकऔषधियाँजैव प्रौद्योगिकीस्वास्थ्य सेवा
Ascendis Pharma एक फार्मास्युटिकल और जैव-प्रौद्योगिकी कंपनी है, जो गंभीर अपूर्ण चिकित्सा आवश्यकताओं के लिए उपचार विकसित करती है और जिसका विशेष ध्यान एंडोक्राइनोलॉजी तथा ऑन्कोलॉजी पर है। इसका स्वामित्व वाला TransCon प्रौद्योगिकी प्लेटफ़ॉर्म एक ऐसी पाइपलाइन को समर्थन देता है जिसमें दुर्लभ अंतःस्रावी रोगों के लिए TransCon PTH और TransCon CNP, साथ ही TransCon TLR7/8 Agonist जैसे ऑन्कोलॉजी कार्यक्रम शामिल हैं। कंपनी दुनिया भर के रोगियों, देखभालकर्ताओं और चिकित्सकों के लिए रोगी-केंद्रित उपचारों को आगे बढ़ाने और परिणामों में सुधार करने हेतु वैज्ञानिक तथा स्वास्थ्य सेवा विशेषज्ञता को एक साथ लाती है।
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कंपनी की नौकरियाँ

Clinical Scientist, Endocrine Clinical Development – Princeton Hybrid

Lead and oversee late-phase endocrine clinical trials at Ascendis Pharma in a hybrid Princeton role. Analyze clinical data, support regulatory submissions, and advance therapies addressing unmet medical needs.

USसंयुक्त राज्यNJन्यू जर्सी
$1,60,000 – $1,80,000 / वर्ष
हाइब्रिडपूर्णकालिकमध्य स्तरवरिष्ठआवश्यक भाषा: अंग्रेज़ीनैदानिक अनुसंधान

विवरण

  • Lead clinical trial design, oversight, and site and participant retention efforts
  • Coordinate completion of protocols, investigator brochures, monitoring plans, site training materials, study reports, health authority responses, standard operating procedures, and related documentation
  • Contribute to study and cross-functional teams under the direction of the Vice President of Clinical Development
  • Standardize terminology and evaluation criteria across endocrine development programs
  • Protect study integrity while monitoring accumulating safety and efficacy data
  • Identify potential trial barriers and develop practical solutions
  • Analyze and evaluate clinical data to support accurate interpretation and reporting
  • Prepare and review clinical documents, manuscripts, presentations, and regulatory submissions
  • Keep current with relevant science, medical information, good clinical practice, and regulatory requirements
  • Partner with cross-functional teams as a clinical research resource to improve product development
  • Build productive relationships with investigative sites, clinical consultants, and key opinion leaders
  • Contribute to company strategy and organizational initiatives
  • Provide support for commercial activities when needed
  • Deliver assigned work accurately, completely, and on schedule
  • Follow rigorous ethical standards in all activities
  • Travel domestically and internationally for scientific meetings, up to 20% of the time

आवश्यकताएँ

  • Advanced degree such as a Ph.D., Pharm.D., M.S., or equivalent qualification
  • Demonstrated record of scientific and clinical investigation
  • Working knowledge of statistical principles and clinical trial design
  • Understanding of how nonclinical findings inform clinical data
  • Excellent written and verbal communication abilities
  • Ability to learn quickly and follow complex instructions under pressure
  • Strong multitasking, organization, and attention to detail
  • Reliable, collaborative, and hardworking team contributor
  • Initiative and problem-solving ability for moderately complex issues
  • Sound judgment when managing complex, confidential, and regulated information
  • Ability to lead through both direct action and example

लाभ

  • 401(k) plan with company matching contributions
  • Medical, dental, and vision coverage
  • Company-provided life and accidental death and dismemberment insurance
  • Company-provided short- and long-term disability coverage
  • Pet insurance and legal insurance options
  • Employee Assistance Program
  • Employee discount program
  • Professional development opportunities
  • Health Savings Account (HSA)
  • Flexible Spending Accounts
  • Various incentive compensation programs
  • Accident, critical illness, and hospital indemnity insurance
  • Mental health resources
  • Paid leave for new parents
  • Eligibility for a discretionary annual bonus or incentive compensation plan
  • Eligibility for discretionary stock-based long-term incentives
  • Paid time off
  • Comprehensive benefits package
  • Hybrid work arrangement from the Princeton, New Jersey office, with remote consideration for the right candidate

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