Job Advertisement: Non-clinical Specialist
Location: Helsinki (Meilahti)
Position Type: Full-Time
Application Deadline: 09.01.2026
Summary:
Arivin therapeutics seeks a Non-Clinical Specialist to design and oversee non-clinical studies, manage CROs, and prepare regulatory documentation for innovative antimicrobial therapies. Candidates should have a Master’s or Ph.D. in a relevant field and experience in drug development and regulatory toxicology. We offer a collaborative, supportive environment with opportunities to impact the fight against antimicrobial resistance.
About ArivinTx:
At Arivin therapeutics Oy, we focus on Future-Proof antimicrobial strategies: therapies designed to effectively treat resistant bacterial pathogens, without promoting rapid resistance themselves. We prioritize indications where the complications as a result of resistance development are most severe (i.e. chronic infections) and where the need for novel therapies is the most urgent according to the World Health Organization Top Priority list. Unlike traditional antibiotics, our therapies provide a more sustainable solution that helps address the worldwide threat of bacterial resistance and withstand the test of time.
Our company was founded by scientists, meaning that our roadmap is determined by innovative research—not the sales department. We prioritize scientific accuracy and reliability over rushed results.
What we are looking for:
We are looking for a Non-Clinical Specialist to join our team and play a pivotal role in ensuring that our molecules meet regulatory requirements throughout the drug development process—from hit-to-lead selection to clinical trials. This is a unique opportunity to contribute to the development of innovative therapies while shaping non-clinical strategies that directly impact patient outcomes.
In this role, you will have a special focus on non-clinical regulatory studies, including safety, pharmacokinetics (PK), and ADME, as well as the preparation of high-quality documentation and study strategies aligned with the target indication and patient population. You will work closely with your colleagues and development partners to design, execute, and optimize studies that support regulatory submissions and scientific objectives.
A key part of this position involves building and managing strong relationships with CROs, regulatory agencies, biopharma partners, and other ecosystem stakeholders. You will also have the opportunity to identify and pursue new initiatives that drive the company’s scientific and strategic goals forward.
You will work closely with a dynamic, collaborative, and highly driven research team, supporting ongoing projects while also taking ownership of independent tasks. The role requires a strong sense of responsibility, attention to detail, and the ability to adapt to evolving priorities in a fast-paced research environment.
If you are passionate about pioneering new solutions in infectious disease treatment, we invite you to join us on this exciting journey.
Your challenge:
● Design and Strategy: Draft non-clinical drug development plans aligned with timelines, regulatory requirements, the intended indication, and patient population.
● CRO Management: Evaluate and manage CROs for non-clinical studies, including contracting and relationship management.
● Study Oversight: Ensure studies comply with protocols, guidelines, and quality standards. Monitor progress and address issues to guarantee timely completion.
● Data Review: Review and advice on study results, generate cross-study summaries, and draw scientific conclusions.
● Regulatory Documentation: Prepare study summaries, cross-study analyses, and materials for regulatory meetings.
● Collaboration: Work with internal teams to integrate non-clinical findings into drug development strategies and regulatory submissions. The role reports directly to the Chief Scientific Officer (CSO).
Qualifications and Experience:
● Master’s or preferably Ph.D degree in Pharmacy, Biochemistry, Molecular Biology, Medical or Veterinary biosciences or equivalent in a relevant field.
● A minimum of 3 years working knowledge of, and experience in, drug development.
● Experience in regulatory toxicology and toxicological tests.
● Knowledge in ICH, OECD test guidelines and FDA and EMA guidance documents.
● Experience with Standard Operating Procedures (SOPs) and quality systems.
● Experience working with CROs or other stakeholders.
● Experience in clinical trials and CMC are seen as benefits.
As a person, we hope that you:
● Plan carefully and align before executing tasks.
● Can independently organize, plan, take initiative and carry out responsibilities.
● Produce scientifically rigorous, well-supported documents, conclusions, and summaries.
● Pay close attention to detail, demonstrate strong organizational skills, and maintain a solid work ethic.
● Are adaptable and willing to take on a variety of tasks typical in a start-up environment.
● Have excellent command of English, both written and spoken.
● Collaborate effectively with team members and contribute positively to the working environment.
Are you missing some of the above-mentioned skills? Don't worry, we also developed some of them while working and we can provide guidance and/or training on specific topics. However, solid knowledge of drug development is vital.
What We Offer:
● Science that can make a difference. Antimicrobial resistance is rapidly becoming one of the biggest medical and societal challenges of our time, with 4.7 million associated deaths in 2021, a number that is still rapidly rising. Arivin Tx works on cutting-edge research to change the outcome of this crisis.
● A competitive salary. As we search for excellent team members, we provide a salary to match it.
● A supportive learning environment. As we are pioneering novel antimicrobial therapies, we all have lots to learn along the way. We provide additional opportunities such as courses and/or attendance to international conferences to catch up on the latest research developments.
● Fun and diverse working environment. Arivin Tx was created by four founders from four different countries. We are positive-minded scientists that are passionate about fighting back against this global resistance crisis. We have created a culture where ideas can be shared and challenged, no matter your title or background.
● Balanced working environment. Although our ambitions high, we make sure that this ambition does not come at a cost. We have our team’s well-being as a priority. We offer a collaborative and flexible working environment and actively ensure work-life balance by promoting sports, culture and wellbeing activities with company benefits.
Legal authorization to work in Finland is required for this position. We cannot sponsor employment visas.
How to Apply:
Please send your CV and a cover letter detailing your qualifications and motivation for this role to Recruitments@arivintx.com. Applications are reviewed on an ongoing basis.
If you have additional questions, we will be available to answer them during the following time slots: 18/12/2025 from 10:00-13:00
07/01/2026 from 10:00-13:00
Please contact info@arivintx.com with your preferred date and time.
Join us in making an impact in microbiological research!
