Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Drive innovative clinical strategies and author key documents for groundbreaking research.
- Company: Join a pioneering biotech firm focused on transforming healthcare.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Why this job: Make a real impact in clinical research and contribute to life-changing therapies.
- Qualifications: Advanced scientific degree and experience in early clinical development required.
- Other info: Collaborative environment with a focus on innovation and career advancement.
The predicted salary is between 36000 - 60000 ÂŁ per year.
The Clinical Research Scientist will report to the VP, Development Strategy & Clinical Operations within the Development team and will collaborate on the development of clinical designs and draft key clinical documents, including the protocol to take Alchemab’s first programmes into the clinic. The role will partner with cross‑functional teams to share early clinical strategy, design fit‑for‑purpose phase I/II studies. The Clinical Research Scientist will author clinical documents and drive scientific data reviews during conduct to accelerate proof of concept decisions (PoC).
Responsibilities
- Strategy Development: Participate actively to the gap assessment to any “bound‑for‑clinic” program and translate findings into pragmatic clinical designs. Research and define clinically meaningful endpoints (including exploratory/digital/biomarker endpoints) and outline timing, feasibility and risk trade‑offs. Work with the Development team (development, Translational and Biomarker Leads) and the Clinical/Regulatory Sub Team (CRST) to develop a recommendation for the PoC strategy. Partner with Commercial team representatives to lead the drafting of the target product profile.
- Strategy Implementation: Draft the Clinical Concept Sheet for usage in Contract Research Organisation (CRO) selection, KOL conversations and other elements. Author/review clinical protocols, amendments and key study tools. Contribute to Clinical Trial Authorisation (CTA) and Investigational New Drug (IND) Application enabling content (clinical sections of Investigators Brochure (IB)). Drive the formation of program‑specific KOL boards to review the protocol and strategy choices.
- Keeping abreast of innovations: Researching and educating the wider Alchemab team on approaches to clinical trial strategy and design. Staying up‑to‑date on innovative approaches to generating rapid PoC data. Understanding the competitive landscape for key therapeutic areas.
- Cross Functional teamwork: Core member of the Development team for select programmes. Member of the Clinical/Regulatory Sub‑Team (CRST) for select programmes, with potential to chair. Member of RFP/vendor selection groups and internal/external Clinical Trial Teams. Act as a delegate, where appropriate, for the CMO/Medical lead.
Essential
- Advanced scientific training (PhD, PharmD, MD or equivalent) or MSc with strong industry experience.
- Solid track record in early clinical development (FIH/Phase 1/2) within biotech, pharma or CRO.
- Demonstrated authorship of clinical protocols and related study documents; familiarity with GCP and UK/EU/US regulatory pathways (CTA/IND).
- Experience with medical data review and study interpretation; comfortable building slides and presenting to senior/internal and external audiences.
- Strong understanding of biotech product development processes, regulatory requirements, and market dynamics.
- Exceptional communication and interpersonal skills, with the ability to collaborate effectively with internal and external stakeholders.
NOTE: This job description is not intended to be all inclusive. Employees may perform other related duties as negotiated to meet the ongoing needs of the organisation.
Clinical Research Scientist in Cambridge employer: Alchemab Therapeutics
Contact Detail:
Alchemab Therapeutics Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Scientist in Cambridge
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research 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 clinical research. 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, like clinical protocols or presentations, to interviews. This will help us see your skills in action and 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 us you’re genuinely interested in being part of our team.
We think you need these skills to ace Clinical Research Scientist in Cambridge
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter to highlight your relevant experience in clinical research. We want to see how your background aligns with the role of Clinical Research Scientist, so don’t hold back on showcasing your skills!
Showcase Your Writing Skills: Since you'll be drafting key clinical documents, it's essential to demonstrate your writing prowess. Include examples of protocols or study documents you've authored in your application to give us a taste of your capabilities.
Highlight Teamwork Experience: Collaboration is key in this role, so share instances where you've worked effectively in cross-functional teams. We love to see how you’ve partnered with others to achieve common goals in your previous roles.
Apply Through Our Website: We encourage you to submit your application through our website for a smoother process. It helps us keep everything organised and ensures your application gets the attention it deserves!
How to prepare for a job interview at Alchemab Therapeutics
✨Know Your Clinical Stuff
Make sure you brush up on your knowledge of early clinical development, especially FIH and Phase 1/2 studies. Be ready to discuss your experience with drafting clinical protocols and any relevant regulatory pathways like CTA and IND. This will show that you’re not just familiar with the theory but have practical insights too.
✨Showcase Your Collaboration Skills
Since this role involves working with cross-functional teams, prepare examples of how you've successfully collaborated in the past. Think about specific projects where you partnered with different departments or stakeholders, and be ready to share how you navigated challenges together.
✨Be Ready to Discuss Strategy
The interviewers will want to know how you approach strategy development. Prepare to talk about how you assess gaps in clinical programmes and translate findings into actionable designs. Having a few examples of clinically meaningful endpoints you've defined will really help you stand out.
✨Stay Current with Innovations
Demonstrate your commitment to staying updated on the latest trends in clinical trial strategy and design. Bring up any recent innovations you've researched or implemented in your work. This shows that you're proactive and genuinely interested in advancing the field.