At a Glance
- Tasks: Analyse large-scale genetic data to improve patient identification for rare diseases.
- Company: Join BioMarin, a leader in biotechnology focused on transformative medicines.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Why this job: Make a real impact on patients' lives through innovative genomic research.
- Qualifications: PhD in bioinformatics or related field; strong analytical and programming skills required.
- Other info: Collaborate with diverse teams and contribute to groundbreaking drug discovery.
The predicted salary is between 36000 - 60000 £ per year.
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need.
We are seeking a Scientist II to join the Genomics team to support late‑stage clinical programs and post‑marketing efforts to help improve patient identification. This role will have a direct impact on patients’ lives by helping us to better understand where our patients are around the world. The successful candidate will have the opportunity to contribute to patient identification efforts as part of our Enzyme Replacement Therapy Business Unit.
In particular, the candidate’s efforts will focus on:
- Estimating disease prevalence of rare autosomal recessive disorders from genetic data to identify regions of the globe with high disease burden.
- Understanding the mutation spectrum that underpins these diseases.
- Resolving variants of uncertain significance to improve diagnostic outcomes.
This is an opportunity to work with dynamic, cross‑functional teams where you can apply your expertise in statistical genetics and bioinformatics to contribute to the broader enterprise’s mission of finding and treating people affected with rare disease. You will collaborate with experts across a wide range of functions, including across Research & Development, as well as in our Global Medical Affairs and Commercial organizations. You will also work with external collaborators to expand our expertise in patient identification and mutation annotation.
Most importantly, you will have a chance for your work to have immediate impact on a fast‑moving drug discovery and development process, to improve the lives of patients.
RESPONSIBILITIES
- Oversee the analysis of large‑scale sequencing data in external cohorts of patients, working with academic and commercial partners to estimate disease prevalence of rare autosomal recessive diseases and support efforts in identifying patients around the world.
- Merge diverse sources of genotype‑phenotype information, including in vitro data, and apply state‑of‑the‑art annotation methods for determining mutation pathogenicity.
- Communicate discoveries to internal colleagues with a variety of backgrounds and to the wider scientific community through presentations or publications.
- Collaborate with internal colleagues across a variety of functions and backgrounds to understand the critical needs of the Enzyme Replacement Therapy Business Unit and deliver on those goals using genetic and genomic data.
- Evaluate bioinformatic and in vitro methods for resolving variants of uncertain significance (‘VUSs’); coordinate with external partners to execute translational assays for assessing variants of uncertain significance.
- Act as a leader for and provide support to more junior members of the team.
EDUCATION AND EXPERIENCE
- PhD in bioinformatics, statistical genetics, computational biology, or a related field (or equivalent).
- Strong analytic skills, including fluency in at least one major programming language (ideally R or Python), and experience working with a high‑performance computing cluster.
- Hands‑on experience managing, analyzing, and interpreting large omics datasets, especially genetic variation data such as sequencing data and data capturing genotype‑phenotype relationships.
- Experience leading your own research projects, particularly those that are collaborative (e.g., spanning multiple sites) and/or cross‑functional (e.g., working and communicating with scientists outside your field of expertise).
- Ability to engage with internal and external partners to understand and identify key scientific questions and assess project priorities.
- A clear track‑record of communicating science, for example through publications or conference presentations.
- Desired: 2+ years of experience post PhD in academia or industry.
This description is not intended to be all‑inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Scientist II employer: BIOMARIN
Contact Detail:
BIOMARIN Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Scientist II
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect with BioMarin employees on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching BioMarin’s latest projects and breakthroughs. Show us that you’re not just interested in the role but also passionate about our mission to improve patient lives through innovative science.
✨Tip Number 3
Practice your pitch! Be ready to explain how your skills in bioinformatics and statistical genetics can directly contribute to our goals. Tailor your examples to highlight your experience with large-scale sequencing data and collaboration.
✨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 us you’re genuinely interested in joining the BioMarin team.
We think you need these skills to ace Scientist II
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the Scientist II role. Highlight your expertise in bioinformatics and statistical genetics, and don’t forget to mention any relevant projects or collaborations you've been part of.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you're passionate about genetic research and how your background makes you a perfect fit for our Genomics team. Be specific about what excites you about working at BioMarin.
Showcase Your Communication Skills: Since you'll be collaborating with various teams, it's crucial to demonstrate your ability to communicate complex scientific concepts clearly. Include examples of how you've successfully shared your findings with different audiences, whether through publications or presentations.
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, you’ll find all the details you need about the role and our company culture there!
How to prepare for a job interview at BIOMARIN
✨Know Your Science
Make sure you brush up on the latest advancements in genomics and bioinformatics. Be prepared to discuss how your expertise aligns with BioMarin's mission to tackle rare genetic diseases. Familiarise yourself with their current projects and be ready to share your insights on how you can contribute.
✨Showcase Your Analytical Skills
Since the role requires strong analytic skills, come prepared with examples of how you've managed and interpreted large datasets. Highlight your experience with programming languages like R or Python, and be ready to discuss specific projects where you've applied these skills to solve complex problems.
✨Collaboration is Key
BioMarin values teamwork across various functions. Think of instances where you've successfully collaborated with others, especially in cross-functional settings. Be ready to explain how you communicate complex scientific concepts to non-experts, as this will demonstrate your ability to work effectively within diverse teams.
✨Prepare for Questions on VUSs
Given the focus on variants of uncertain significance, prepare to discuss your approach to evaluating and resolving VUSs. Bring examples of how you've coordinated with external partners or used bioinformatic methods to assess mutation pathogenicity, as this will show your hands-on experience in the field.