Be at the heart of actionFly remote-controlled drones into enemy territory to gather vital information.

Apply Now

Graduate Proposal Writer – Clinical Trials (Hybrid Role)

Quotient Sciences Limited
Nottingham
4 days ago
Create job alert

Graduate Proposal Writer – Clinical Trials (Hybrid Role)

Nottingham, UK

Job Description

Posted Thursday 31 July 2025 at 05:00 | Expires Saturday 16 August 2025 at 04:59

Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we help biotech and pharma customers save precious time and money in getting drugs to patients.

We employ more than 1,100 talented individuals globally, located at state-of-the-art development, manufacturing and clinical facilities in the UK and USA. Science, Agility and Culture are the core components that define Quotient Sciences, enabling us to do what we do in the way that we do it.

People join Quotient Sciences because we are a respected member of the drug development communitythat’s focused on innovation and are driven by an unswerving belief that ideas need to become solutions, and molecules need to become cures, fast. Because humanity needs solutions, fast.

Are you a recent Life Sciences graduate with a passion for clinical research and a knack for detail? Join our Client Services team and help shape the future of clinical trials from the ground up.

About the Role

As a Graduate Proposal Writer, you’ll support our Commercial teams in winning new business by contributing to project scoping, proposal writing, costings, and client communications. This is anentry-level rolewithfull in-house trainingandexcellent career progression.

  • Lead and manage the generation of ballparks, costings, and proposals for selected opportunities.
  • Liaise with internal stakeholders and third-party vendors to gather information for Requests for Proposals (RFPs).
  • Compile and generate data to populate client-defined bid grids.
  • Create budgets for change orders on signed projects.
  • Attend and complete training activities relevant to proposal writing within the assigned commercial line.
  • Support Strategic Partnership deals, including client-specific training, proposal and change order development, and participation in internal calls.
  • Identify and implement efficiency improvements in costing and proposal processes.
  • Maintain and update proposal and costing model templates.
  • Ensure accurate and up-to-date usage of Salesforce to track departmental metrics and commercial data.
  • Participate in company initiatives such as the Health & Safety Committee and S&I outreach.

Job Demands

This role may involve:

  • High concentration and attention to detail.
  • Working to strict and tight deadlines.
  • Managing multiple tasks simultaneously.
  • Occasional work outside normal hours.
  • Adhering to safety procedures in potentially hazardous environments.
  • Responding to client demands promptly and professionally.

What You’ll Need

  • ABSc in Life Sciences(or equivalent).
  • A basic understanding ofclinical trial processes, especially Phase 1/2 programmes.
  • Proficiency inMicrosoft Excel, Word, and PowerPoint.
  • Strong communication and presentation skills.
  • A proactive, organised, and collaborative mindset.

What You’ll Gain

  • Hands-on experience in proposal development and commercial operations.
  • Exposure to pharmaceutical sciences, clinical conduct, and data sciences.
  • Training in GXP guidelines and internal systems.
  • A hybrid working model for flexibility and balance.
  • A clear path for career development in a growing organisation.

Ready to launch your career in clinical trials?
Apply now and become part of a team that’s transforming healthcare through innovation and collaboration.

Application Requirements

When applying for a position with Quotient Sciences to be able to work in our organisation you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.

Our Commitment to Diversity, Equity and Inclusion

Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organisation. As a global employer, we recognise the value in having an organisation that is a true reflection and representation of our society today.

Specifically we will not discriminate on the basis of race, colour, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.

This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.


#J-18808-Ljbffr

Related Jobs

View all jobs

Regulatory Affairs Project Manager

Advanced Specialist Pharmacist, Clinical Trials

Advanced Specialist Pharmacist, Clinical Trials

Graduate Metrology & Measurement Engineer – Training Opportunity

Graduate Sales Representative

Graduate Process Development Engineer

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Medical Technology Recruitment Trends 2025 (UK): What Job Seekers Need To Know About Today’s Hiring Process

Summary: UK medical technology hiring has shifted from title‑led CV screens to capability‑driven assessments that emphasise regulatory‑aware product delivery (QMS, ISO 13485), software lifecycle & risk (IEC 62304/14971), usability (IEC 62366), clinical & regulatory strategy (MDR/UKCA), device cyber security & privacy, and measurable patient/clinical and commercial impact. This guide explains what’s changed, what to expect in interviews & how to prepare—especially for SaMD engineers, AI/ML in medical devices, product & quality engineers, regulatory/clinical affairs specialists, validation/verification, manufacturing/operations, and digital health roles. Who this is for: Software/firmware engineers in medtech, SaMD/AI engineers, systems & verification engineers, quality & regulatory affairs (QARA), clinical evaluation/PMCF specialists, human factors engineers, medical device cyber security & privacy, test/validation, manufacturing & operations, field/service engineers, and medtech product managers in the UK.

Why Medical Technology Careers in the UK Are Becoming More Multidisciplinary

Medical technology (medtech) is transforming healthcare in the UK — from wearable sensors to AI diagnostic tools, from surgical robots to telemedicine platforms. Advances in hardware, software, data and connectivity are enabling more personalized, efficient and accessible care. But with great power comes great responsibility. As medical devices and health technologies enter hospitals, clinics and consumers’ homes, professionals in this domain must master much more than engineering and algorithms. They must also understand law, ethics, psychology, linguistics & design. That is, medtech careers are now deeply multidisciplinary. In this article, we explore why medical technology careers in the UK are becoming more multidisciplinary, how these five allied fields now intersect with medtech work, and what job-seekers and employers should do to succeed in this evolving ecosystem.

Medical Technology Team Structures Explained: Who Does What in a Modern MedTech Department

Medical technology (MedTech) spans everything from wearable health devices and surgical robots to diagnostic imaging, in-vitro diagnostics (IVD), digital therapeutics, AI-driven triage, and Class I–III medical devices. In the UK, the sector touches NHS care pathways, private providers, and global markets—with stringent expectations for safety, clinical evidence, cybersecurity, and data privacy. As ventures scale from prototype to regulated product, clear team structures become the difference between promising pilots and licensed, market-ready devices. Whether you’re hiring your first clinical specialist or applying for a role in QA/RA, this guide explains who does what in a modern MedTech department, how functions collaborate across the product lifecycle, UK-typical skill sets and salaries, common pitfalls, and best practices for building a resilient team.