At a Glance
- Tasks: Coordinate and manage innovative drug development studies with global partners.
- Company: Leading biotechnology firm focused on humanised in vivo models.
- Benefits: Competitive salary, professional growth, and supportive team environment.
- Other info: Dynamic role with excellent career progression opportunities.
- Why this job: Make a real impact in drug development while collaborating with top researchers.
- Qualifications: PhD and experience in managing scientific projects required.
The predicted salary is between 50000 - 65000 £ per year.
STEM Recruitment is seeking a dedicated Senior Scientist / Study Manager for our client based in Dundee, Scotland. Our client is an innovative biotechnology company focused on humanised in vivo models and tools for advancing the drug development paradigm and predicting drug-drug interactions in patients. In this essential role, you will collaborate with global clients, research institutes, drug regulators such as the MHRA, and philanthropic foundations such as the Bill & Melinda Gates Foundation.
We are now seeking a highly organised and proactive Senior Scientist / Study Manager to coordinate and deliver project activities under the Gates-funded programme. This role is central to ensuring that studies using the humanised mouse model are efficiently planned, executed, tracked, and reported in alignment with grant commitments and partner expectations.
Role overview
The Senior Scientist / Study Manager will support the delivery of studies for Gates funded researchers working closely with scientists, external collaborators, and partner organisations. This role requires exceptional organisational skills, attention to detail, and the ability to manage multiple scientific workstreams simultaneously. This is a hands-on operational role that sits at the heart of the in vivo and translational research portfolio.
Key Responsibilities
- Study Coordination & Planning: Manage day-to-day planning and scheduling of studies conducted under the Gates grant. Coordinate study protocols, experimental timelines, resource requirements, and logistics. Ensure alignment between scientific plans and available animal, staffing, and facility capacity.
- Operational Oversight: Track study progress, milestones, and deliverables, ensuring timely execution, maintain detailed study documentation including protocols, amendments, and internal records. Support coordination of sample handling, data capture, and study-related workflows.
- Communication & Collaboration: Liaise effectively with internal scientists, external collaborators, Gates-funded partners, and other stakeholders. Facilitate study meetings, prepare agendas, and circulate action logs. Ensure that all parties remain updated on timelines, dependencies, and required inputs. Manage the resolution of any issues that arise during the execution of the projects.
- Data & Reporting: Support scientific team in assembling data packages and reports for funders and collaborators. Maintain accurate and audit-ready study files. Assist with drafting operational sections of progress reports to the Bill & Melinda Gates Foundation.
- Quality & Compliance: Ensure adherence to internal SOPs and ethical standards relating to in vivo work. Support continuous improvement in study coordination processes.
Skills & Experience
Required Experience & Attributes: PhD qualified, plus experience in managing scientific projects, within a life sciences CRO, biotech or pharmaceutical setting. Strong organisational skills with proven ability to manage multiple concurrent activities. Excellent communication skills and confidence working across multidisciplinary teams. Detail-oriented, reliable, and comfortable maintaining structured documentation. Expert knowledge of the drug development paradigm, and specifically in drug metabolism and pharmacokinetics.
Desirable Additional Skills: Project management qualification (e.g. PRINCE2). Familiarity with project management tools (e.g. Motion, Notion, Monday). Familiarity with interdisciplinary engagement. Familiarity with computational models and databases used in drug development.
The role offers a competitive salary package, opportunities for professional growth, and the chance to work within a leading organisation in the biotechnology sector. You will be part of a dynamic team committed to innovative research and development, fostering professional development and career progression in a supportive environment.
Senior Scientist / Study Director. Job in Dundee LilyLifestyle Jobs employer: United Cerebral Palsy of Georgia
Join a pioneering biotechnology company in Dundee, where your role as a Senior Scientist / Study Manager will place you at the forefront of innovative drug development. With a strong emphasis on professional growth and a collaborative work culture, you'll have the opportunity to engage with global partners and contribute to impactful research initiatives. Enjoy a competitive salary package and be part of a dynamic team dedicated to advancing healthcare solutions.
Contact Details:
United Cerebral Palsy of Georgia Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Senior Scientist / Study Director. Job in Dundee LilyLifestyle Jobs
✨Tip Number 1
Network like a pro! Reach out to professionals in the biotech field, especially those who work with humanised models or drug development. Attend industry events or webinars to make connections and learn about potential job openings.
✨Tip Number 2
Show off your skills! Prepare a portfolio that highlights your previous projects and achievements in managing scientific studies. This will give you an edge during interviews and show that you’re ready to hit the ground running.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your responses, especially around your experience with project management and collaboration. The more comfortable you are, the better you'll perform.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can sometimes give you a better chance at landing that dream role. Let’s get you started on this exciting journey!
We think you need these skills to ace Senior Scientist / Study Director. Job in Dundee LilyLifestyle Jobs
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Scientist / Study Manager role. Highlight your relevant experience in managing scientific projects and any specific skills that align with the job description, like your knowledge of drug development and organisational prowess.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your background makes you a perfect fit. Don’t forget to mention your experience with collaboration and communication, as these are key for this position.
Showcase Your Organisational Skills:Since this role requires exceptional organisational skills, be sure to provide examples in your application that demonstrate your ability to manage multiple projects simultaneously. Mention any tools or methods you use to stay organised and efficient.
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates regarding your application status.
How to prepare for a job interview at United Cerebral Palsy of Georgia
✨Know Your Science
Make sure you brush up on the latest advancements in drug development, especially around humanised in vivo models. Being able to discuss recent studies or breakthroughs will show your passion and expertise in the field.
✨Master the Art of Coordination
Since this role involves a lot of project management, be prepared to talk about your organisational skills. Have examples ready that demonstrate how you've successfully managed multiple projects or studies simultaneously.
✨Communication is Key
This position requires liaising with various stakeholders. Think of instances where you've effectively communicated complex scientific information to non-scientists or collaborated with multidisciplinary teams. Highlight your ability to keep everyone on the same page.
✨Be Detail-Oriented
Attention to detail is crucial in this role. Prepare to discuss how you ensure accuracy in documentation and compliance with ethical standards. Bring examples of how your meticulous nature has positively impacted previous projects.
