-
Lek, a Sandoz company
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Senior Scientist Clinical Development (d/f/m)
Slovenia
· Full-time
·
Mid-Senior
Job Description
More than 60! Is the number of clinical trials that global clinical team design, manage, monitor and support each year within our clinical team in order to ensure good clinical practice, trial subjects’ safety, and robust data for drug development. Join us in connecting science with clinical procedures in practice.
As Senior Scientist Clinical Development (d/f/m) you will be responsible for planning, execution, data analysis and reporting of complex bioequivalence and Phase III clinical trials on patients that should be executed on time, within budget and in compliance with Sandoz processes and regulatory requirementsAlso you will be responsible for the preparation of clinical development strategy for new product in close collaboration with the project team, preparation of product registration documentation and interactions with health authorities in context of clinical studies. It is our expacation that candidate will work in accordance with legislation, internal rules, good practices and business objectives of the company..
Your Key Responsibilities
Your responsibilities include, but not limited to:
What you will bring to the role:
Employment at the most reputable employer in Slovenia offers Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical, mental and social well-being (Energized for Life), Unlimited learning and development opportunities.
Possible job locations: Slovenia (Ljubljana)
We offer permanent contract with 6-month of probation period. You are kindly invited to submit your application in English language, including CV, by 27.3.2025.
Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!
The future is ours to shape!
Commitment To Diversity & Inclusion
Sandoz is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.
Join Our Sandoz Network
If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Sandoz and our career opportunities, join the Network here: https://talentnetwork.novartis.com/sandoztalentpool
#Sandoz
More than 60! Is the number of clinical trials that global clinical team design, manage, monitor and support each year within our clinical team in order to ensure good clinical practice, trial subjects’ safety, and robust data for drug development. Join us in connecting science with clinical procedures in practice.
As Senior Scientist Clinical Development (d/f/m) you will be responsible for planning, execution, data analysis and reporting of complex bioequivalence and Phase III clinical trials on patients that should be executed on time, within budget and in compliance with Sandoz processes and regulatory requirementsAlso you will be responsible for the preparation of clinical development strategy for new product in close collaboration with the project team, preparation of product registration documentation and interactions with health authorities in context of clinical studies. It is our expacation that candidate will work in accordance with legislation, internal rules, good practices and business objectives of the company..
Your Key Responsibilities
Your responsibilities include, but not limited to:
- Active participation in development of formulations.
- Setting clinical strategy (HV or patient studies).
- Independently plan, manage, and oversee clinical studies in accordance with project strategy, resources, timelines, and regulatory and professional standards.
- Responsibility for GxP standard implementation and ensuring that these standards are trained on, known, and understood, and that implementation is controlled.
- Ensures GCP audit readiness.
- Contribute as a member of the clinical development team to continuous harmonization, process improvement initiatives, knowledge sharing, and setting of the excellence framework for clinical research, as well as contributing to implementing the vision and strategy for Product development small molecule clinical development.
- Responsibility for continuous personal and professional development (knowledge, skills, behaviors).
What you will bring to the role:
- University degree (BSc) in pharmacy, medicine or other related natural science.
- Minimum 3 years experience in clinical development or associated fields.
- Good knowledge of Good Clinical Practice (GCP).
- Good communication and organizational skills.
- Fluent in English (oral and written).
- Knowledge of Microsoft Office.
Employment at the most reputable employer in Slovenia offers Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical, mental and social well-being (Energized for Life), Unlimited learning and development opportunities.
Possible job locations: Slovenia (Ljubljana)
We offer permanent contract with 6-month of probation period. You are kindly invited to submit your application in English language, including CV, by 27.3.2025.
Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!
The future is ours to shape!
Commitment To Diversity & Inclusion
Sandoz is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.
Join Our Sandoz Network
If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Sandoz and our career opportunities, join the Network here: https://talentnetwork.novartis.com/sandoztalentpool
#Sandoz
Key Skills
Ranked by relevance
data analysis
gcp
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- Posted
- Mar 21, 2025
- Type
- Full-time
- Level
- Mid-Senior
- Location
- Ig
- Company
- Lek, a Sandoz company
Industries
Pharmaceutical Manufacturing
Categories
Research
Analyst
Information Technology
Related Jobs
3 roles aligned with this opportunity
View Job Details
Related
Raziskovalec v laboratoriju skupine IVIVC (d/ž/m) / Laboratory Scientist in IVIVC group (d/f/m)
2026-05-22
Full-time
Not Applicable
Slovenia
Pharmaceutical Manufacturing
Research
View Job Details
Related
Product Analyst - Singapore
2026-05-24
Full-time
Not Applicable
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Research
View Job Details
Related
Machine Learning Engineer II
2026-05-23
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