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Toxicologist/Non-Clinical Safety Specialist

Are you passionate about bringing safe and efficacious drugs to patients? Do you have experience within Non-Clinical Safety and Toxicology?

If so, now is your chance to join Ascendis Pharma as our new Toxicologist/Non-Clinical Safety Specialist.

Ascendis Pharma is a fast-growing global biopharmaceutical company committed to making a meaningful difference in patients’ lives. We have locations in Denmark, Germany, the United States, the UK, Italy, Spain, France, and Switzerland.

Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new therapies, selecting only those that demonstrate best-in-class potential to address unmet medical needs.

Today, we are advancing programs in Endocrinology Rare Disease and Oncology. In addition, we collaborate with partners around the world on the development of TransCon-based products for other therapeutic areas and markets.

We are seeking a passionate colleague to join our growing team. As a member of the Ascendis Pharma team, you will play a crucial role in supporting Ascendis Pharma’s growing pipelines with non-clinical safety evaluations, particularly the monitoring of non-clinical studies conducted at CROs. This is an exciting opportunity to work in a fast-paced environment, collaborate with cross-functional, global teams working together to achieve extraordinary results.

You will be joining 12 passionate colleagues within the Pharmacology and Toxicology Area, many of whom have been with Ascendis for several years. You will report directly to Kristin Laura Abel, Vice President of Pharmacology and Toxicology, based in Hellerup where you also will be based.

Your key responsibilities will be:

  • Independently and timely manage high quality non-clinical in vitro and in vivo safety assessment studies or analyses in compliance with all safety, regulatory and GLP requirements in collaboration with internal and/or external stakeholders
  • Participate in non-clinical project teams with multi-disciplinary regional and global members, that develop and execute on the non-clinical safety/development strategy, and provide key input to the development of regulatory strategies
  • Delivering timely and high-quality non-clinical safety evaluations to our programs, including input to early-stage projects
  • Supporting regulatory interactions, clinical trials and product registrations with Non-Clinical Safety input

Qualifications and Skills:

You hold a relevant academic degree – preferably a MSc or PhD within Veterinary Medicine, Pharmaceutical Sciences, or other Life Sciences.

Furthermore, you:

  • Have solid knowledge of animal physiology and pathology combined with a strong scientific mindset
  • Work in a structured way to keep track of multiple timelines - GLP experience is an advantage
  • Enjoy being challenged with new tasks and are a quick learner
  • Have good oral and written communication skills in English

Key competencies:

You are a strong team player, analytical, and have a can-do attitude with good collaboration skills to establish professional engaging relations internally and externally.

You possess an entrepreneurial mindset and can thrive in an informal, open environment where innovation and change are key.

To succeed in this role, we also expect you to

  • Work from the Hellerup office to facilitate interacting with your colleagues
  • Be proactive and self-motivated with a strong drive, able to work in a dynamic environment, and capable of managing multiple objectives in parallel while adapting to changing priorities
  • Be willing to prioritize high ethical standards for animal studies sponsored by Ascendis Pharma

Travel: Up to 15 days per year.

Office: Tuborg Boulevard 12, 2900 Hellerup 

Apply now.

Applications will be evaluated when received, so please apply as soon as possible.

All applications must be submitted in English and are treated confidentially.

 

The job level will be based on your previous experience within Non-Clinical Safety and/or Toxicology.

 

For more details about the position or the company, please contact Kristin Laura Abel, kla@ascendispharma.com

 

You can learn more about Ascendis by visiting our website www.ascendispharma.com

Applications submitted via email or other channels will not be reviewed.

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What You Should Know About Toxicologist/Non-Clinical Safety Specialist, Ascendis Pharma

Are you ready to make a significant impact in the world of biopharmaceuticals? Join Ascendis Pharma as a Toxicologist/Non-Clinical Safety Specialist, where your expertise will play a vital role in ensuring the safety and efficacy of new therapeutic developments. At Ascendis Pharma, a dynamic and rapidly growing company, we are driven by our commitment to Patients, Science, and Passion, aiming to improve lives through innovative therapies. As part of our team, you'll embrace a crucial position within the Pharmacology and Toxicology area, working alongside passionate colleagues who share your enthusiasm for enhancing patient outcomes. Your role will involve managing high-quality non-clinical safety assessment studies and collaborating on the development of regulatory strategies. We seek individuals with a strong academic background in Veterinary Medicine, Pharmaceutical Sciences, or related Life Sciences, who thrive in a fast-paced, collaborative environment. If you have solid knowledge of animal physiology, are meticulous about timelines, and possess excellent communication skills, then you’ll fit perfectly into our team. Embrace the opportunity to grow your career as you contribute to Ascendis Pharma’s mission, supporting exciting projects in Endocrinology, Rare Diseases, and Oncology. With an emphasis on high ethical standards and a can-do attitude, this position offers not just a job, but a chance to be a part of something larger—transforming lives through scientific advancement. Ready to take that next step? Apply now and be a part of our exciting journey!

Frequently Asked Questions (FAQs) for Toxicologist/Non-Clinical Safety Specialist Role at Ascendis Pharma
What are the core responsibilities of a Toxicologist/Non-Clinical Safety Specialist at Ascendis Pharma?

As a Toxicologist/Non-Clinical Safety Specialist at Ascendis Pharma, your main responsibilities will include managing non-clinical safety assessment studies, collaborating with multidisciplinary teams, and contributing to regulatory strategies and project evaluations. You’ll play a key part in ensuring all studies comply with safety and GLP requirements while focusing on the high quality of safety evaluations to support innovative therapies.

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What qualifications are needed for the Toxicologist/Non-Clinical Safety Specialist position at Ascendis Pharma?

To qualify for the Toxicologist/Non-Clinical Safety Specialist role at Ascendis Pharma, you typically need an MSc or PhD in Veterinary Medicine, Pharmaceutical Sciences, or a related Life Science field. Strong knowledge of animal physiology and pathology, alongside good communication skills in English, is essential for success in this position.

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How does the Toxicologist/Non-Clinical Safety Specialist contribute to regulatory interactions at Ascendis Pharma?

In the role of Toxicologist/Non-Clinical Safety Specialist at Ascendis Pharma, you’ll provide critical input for regulatory interactions involving clinical trials and product registrations. Your expertise will help shape the non-clinical safety component of regulatory strategies, ensuring compliance and support for our therapeutic advancements.

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What skills are most important for a successful Toxicologist/Non-Clinical Safety Specialist at Ascendis Pharma?

Success as a Toxicologist/Non-Clinical Safety Specialist at Ascendis Pharma relies heavily on being analytical, structured, and a team player. You should possess a strong scientific mindset, effective communication skills, and the capacity to manage multiple timelines in a fast-paced, changing environment.

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What kind of work environment can a Toxicologist/Non-Clinical Safety Specialist expect at Ascendis Pharma?

At Ascendis Pharma, the work environment is dynamic and encourages innovation and collaboration among team members. You’ll be part of an informal and engaging workplace that emphasizes a proactive attitude and provides exciting opportunities for growth, making it well-suited for individuals with a passion for science and patient care.

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Common Interview Questions for Toxicologist/Non-Clinical Safety Specialist
Can you describe your experience with non-clinical safety assessment studies?

In answering this question, focus on specific examples from your previous work where you managed or contributed to non-clinical safety assessment studies. Highlight your understanding of GLP regulations and how you ensured compliance while delivering quality outcomes.

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What knowledge do you have of animal physiology and pathology relevant to this role?

Discuss your academic background and any relevant experience in animal physiology and pathology. Be detailed about how this knowledge informs your understanding of non-clinical safety assessments and why it is crucial in drug development.

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How do you prioritize timelines when managing multiple projects?

Provide a structured approach to time management. Discuss tools or methods you use to track progress and how you adapt your priorities based on project needs while ensuring high-quality outcomes.

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Describe a challenging situation you faced in safety evaluation and how you handled it.

Share a specific instance where you encountered challenges in the safety evaluation process. Explain the steps you took to address it, focusing on collaborative efforts and effective problem-solving strategies.

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How do you ensure effective communication within a multidisciplinary team?

Emphasize the importance of clear and open communication in collaborative environments. Discuss your strategies for fostering dialogue among team members and ensuring everyone is aligned with project goals.

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What is your approach to regulatory interactions regarding safety data?

Talk about your familiarity with regulatory guidelines and how you prepare documentation and data for submissions. Highlight any experience in preparing for audits or interactions with regulatory bodies.

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Can you provide an example of how you have contributed to ethical standards in your work?

Provide an example where you prioritized ethical considerations in animal studies. Discuss the importance of high ethical standards in your practice and how it aligns with Ascendis Pharma's values.

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What motivates you to work in the field of toxicology and non-clinical safety?

Share personal motivations that drive your passion for toxicology and how they align with the mission of Ascendis Pharma. Discuss your eagerness to contribute to better therapeutic outcomes for patients.

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How do you stay current with developments in toxicology and pharmaceutical safety?

Discuss your commitment to continuous learning, such as attending conferences, reading journals, and participating in professional organizations that focus on toxicology and safety.

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What would you say is the most critical factor for successful non-clinical study management?

Identify key factors such as thorough planning, attention to detail, and effective stakeholder communication. Explain how these contribute to the successful management of non-clinical studies.

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DATE POSTED
April 14, 2025

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