At a Glance
- Tasks: Lead bioanalytical strategy to accelerate transformative medicines for patients worldwide.
- Company: Join a leading biopharma company committed to innovation and patient care.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with opportunities to represent science externally.
- Why this job: Make a real impact in the biopharma industry and shape the future of medicine.
- Qualifications: BSc/MSc or PhD in relevant field with extensive bioanalysis experience required.
The predicted salary is between 70000 - 90000 € per year.
Are you ready to lead bioanalytical strategy that accelerates safe, transformative medicines to patients worldwide? As Associate Director based in Gothenburg, Sweden, you will shape the design and implementation of end-to-end bioanalysis across diverse modalities, translating complex data into clear program decisions that guide dose selection and clinical advancement. You will work at the heart of a collaborative, matrixed environment—partnering closely with lab-based scientists and global project teams to build robust, compliant assays and deliver decisive PK/CK, PD, immunogenicity, and target engagement insights. You will also engage with leaders across discovery, safety, clinical pharmacology, translational science, toxicology, and regulatory, with opportunities to represent our science externally. This role is highly visible and ideal for a scientist who thrives on impact, rigor, and cross‑functional influence.
Accountabilities
- Bioanalytical Strategy Leadership: Define and drive integrated bioanalytical strategies for multiple therapeutic modalities, aligning assay plans with program milestones, dose selection, and decision endpoints to strengthen portfolio progression.
- Experimental Design Partnership: Collaborate with lab-based scientists to shape experimental design, controls, and assay selection that deliver reliable PK/CK, PD, immunogenicity, and target engagement readouts.
- Assay Development and Tech Transfer: Oversee assay development, qualification/validation, and transfer to internal and external labs to ensure reproducibility, scalability, and compliance.
- Regulatory Interface: Prepare and review regulatory documentation; interact with global Health Authorities to address questions, mitigate risks, and enable clinical progress.
- Cross‑Functional Influence: Lead within a matrix environment to integrate bioanalysis across safety, clinical pharmacology, toxicology, translational science, and project teams for cohesive program strategy.
- Risk Management and Quality: Anticipate analytical pitfalls, set data quality standards, and implement controls consistent with regulated bioanalysis to secure decision‑ready data.
- External Representation: Present scientific findings internally and externally, contribute to publications, and represent AstraZeneca in scientific forums and consortia.
- Portfolio Impact: Convert bioanalytical insights into dose decisions and development acceleration, improving the probability of clinical success for patients.
Essential Skills/Experience
- BSc/MSc in relevant subject with extensive experience in Bioanalysis or PhD in relevant subject with strong experience in Bioanalysis required.
- Proven experience as a Subject matter Expert in regulated bioanalysis across a range of modalities PK/CK, PD and immunogenicity assessments (humoral and cellular).
- Experienced as a bioanalytical lead in diverse project teams, defining, leading and implementing robust bioanalytical strategy to advance the portfolio including Biomarker.
Associate Director Integrated Bioanalysis -Biopharma Bioanalytical Program Lead employer: AstraZeneca UK Limited
At AstraZeneca, we pride ourselves on being an exceptional employer, particularly for the role of Associate Director Integrated Bioanalysis in Gothenburg. Our collaborative work culture fosters innovation and cross-functional influence, providing employees with ample opportunities for professional growth and development. With a commitment to advancing transformative medicines, we offer a dynamic environment where your contributions directly impact patient outcomes, supported by a strong focus on compliance and scientific excellence.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director Integrated Bioanalysis -Biopharma Bioanalytical Program Lead
✨Tip Number 1
Network like a pro! Reach out to professionals in the bioanalytical field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to bioanalysis. We recommend doing mock interviews with friends or mentors to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your expertise! Bring along examples of your previous work, such as successful projects or publications, to demonstrate your impact in bioanalysis during interviews. We want to see how you can contribute to our team!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at StudySmarter.
We think you need these skills to ace Associate Director Integrated Bioanalysis -Biopharma Bioanalytical Program Lead
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that align with the Associate Director role. Highlight your bioanalytical expertise and any leadership roles you've had in similar projects. We want to see how you can drive integrated bioanalytical strategies!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about bioanalysis and how your background makes you the perfect fit for this role. Don’t forget to mention your experience in collaborating with cross-functional teams, as that's key for us.
Showcase Your Achievements:When detailing your experience, focus on specific achievements that demonstrate your impact in previous roles. Whether it's successful assay development or regulatory interactions, we love to see quantifiable results that highlight your contributions.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows your enthusiasm for joining our team at StudySmarter!
How to prepare for a job interview at AstraZeneca UK Limited
✨Know Your Bioanalytical Stuff
Make sure you brush up on your knowledge of bioanalytical strategies and methodologies. Be ready to discuss your experience with PK/CK, PD, and immunogenicity assessments in detail. This is your chance to showcase your expertise, so prepare specific examples that highlight your contributions to past projects.
✨Collaborate Like a Pro
Since this role involves working closely with lab-based scientists and cross-functional teams, be prepared to talk about your collaborative experiences. Think of instances where you successfully partnered with others to shape experimental designs or overcome challenges. Highlight your ability to influence and lead within a matrix environment.
✨Regulatory Know-How is Key
Familiarise yourself with the regulatory landscape related to bioanalysis. Be ready to discuss how you've interacted with global Health Authorities in the past, and any experience you have in preparing regulatory documentation. This will show that you understand the importance of compliance and risk management in bioanalytical work.
✨Showcase Your Impact
Prepare to articulate how your bioanalytical insights have led to impactful decisions in previous roles. Think about how you've converted complex data into actionable strategies that improved clinical outcomes. This will demonstrate your ability to drive portfolio progression and make a real difference in the field.
