At a Glance
- Tasks: Lead bioanalytical strategy to accelerate transformative medicines for patients worldwide.
- Company: Join a leading biopharma company dedicated to innovative healthcare solutions.
- Benefits: Competitive salary, collaborative environment, and opportunities for professional growth.
- Other info: Highly visible role with cross-functional influence and excellent career advancement opportunities.
- Why this job: Make a real impact in the biopharma industry while working with cutting-edge science.
- Qualifications: BSc/MSc or PhD in relevant field with extensive bioanalysis experience required.
The predicted salary is between 60000 - 80000 £ per year.
Location: Cambridge
Salary: Competitive
Introduction To Role
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. Can you see yourself aligning innovative assays with program milestones to increase confidence and speed through development? 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
At AstraZeneca, we pride ourselves on being an exceptional employer, particularly for the role of Associate Director Integrated Bioanalysis in Cambridge. 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 competitive salaries, a supportive environment, and the chance to make a significant impact on global health.
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 role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of bioanalytical strategies and recent advancements. We recommend practising common interview questions with a friend to boost your confidence and articulate your expertise.
✨Tip Number 3
Showcase your impact! When discussing your past experiences, focus on specific examples where you’ve driven bioanalytical strategies or led successful projects. We want to see how you can bring that same energy to our team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re excited to see how you can contribute to our mission of delivering transformative medicines.
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 strategies that lead to transformative medicines!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to tell us why you're passionate about bioanalysis and how your background makes you the perfect fit for this role. Be sure to mention specific experiences that demonstrate your ability to lead and influence in a cross-functional environment.
Showcase Your Achievements:When detailing your experience, focus on achievements rather than just responsibilities. Use metrics where possible to illustrate your impact, like how your strategies improved clinical outcomes or accelerated project timelines. We love seeing quantifiable success!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re serious about joining our team at StudySmarter and contributing to our mission of delivering safe, transformative medicines.
How to prepare for a job interview at AstraZeneca
✨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 role is all about translating complex data into actionable insights, so be prepared to showcase how you've done this in past projects.
✨Showcase Your Collaborative Spirit
Since this position involves working closely with lab-based scientists and cross-functional teams, highlight your teamwork skills. Share specific examples of how you've successfully collaborated in a matrix environment to drive bioanalytical strategies forward. They’ll want to see that you can influence and lead within diverse teams.
✨Prepare for Regulatory Conversations
Familiarise yourself with the regulatory landscape related to bioanalysis. Be ready to discuss your experience in preparing regulatory documentation and interacting with health authorities. This shows that you understand the importance of compliance and can navigate potential pitfalls effectively.
✨Demonstrate Your Impact
Think about how your previous work has directly contributed to project success. Prepare to discuss specific instances where your bioanalytical insights led to critical dose decisions or accelerated development timelines. This will help illustrate your value and the impact you can bring to their team.
