Clinical Development Scientist - Vaccines, Manager in Milton Keynes
Clinical Development Scientist - Vaccines, Manager

Clinical Development Scientist - Vaccines, Manager in Milton Keynes

Milton Keynes Full-Time 55000 - 65000 £ / year (est.) No home office possible
Pfizer

At a Glance

  • Tasks: Support global vaccine studies, ensuring safety and scientific integrity.
  • Company: Join Pfizer, a leader in transforming patient lives through innovation.
  • Benefits: Enjoy a hybrid work model, competitive salary, and a culture of flexibility.
  • Why this job: Make a real impact in vaccine development and improve health outcomes.
  • Qualifications: Degree in science or health, with knowledge of clinical research processes.
  • Other info: Diverse and inclusive workplace that values your unique contributions.

The predicted salary is between 55000 - 65000 £ per year.

You will provide clinical and scientific support for global Phase 14 vaccine clinical studies within the Vaccines portfolio. Working in close partnership with clinical colleagues, this role contributes to study design, clinical data review, safety oversight, and scientific integrity across assigned studies.

POSITION RESPONSIBILITIES

  • Maintains current scientific and clinical knowledge in the specific disease area(s) of assignment.
  • Supports development of protocols, informed consent documents, and study-level clinical documentation, with oversight from clinical colleagues.
  • Provides input into study set-up activities, including data collection tools, database design considerations, and clinical data outputs.
  • Reviews and queries clinical study data in line with the clinical data review strategy.
  • Reviews, reports, and manages protocol deviations.
  • In partnership with medically qualified colleagues, supports ongoing safety review activities.
  • Contributes to the review of clinical study reports, regulatory responses, publications, and audit or inspection readiness activities.
  • Collaborates effectively with Clinical Operations, Data Management, Statistics, Regulatory, Medical Writing, and external partners (e.g. CROs, vendors) to ensure timely, compliant study delivery.
  • Ensures trial master file (TMF) compliance for clinical documents.
  • Follows relevant SOPs, regulations, and training requirements; supports continuous improvement initiatives by identifying opportunities to enhance processes, quality, or efficiency within established governance.

REQUIRED QUALIFICATIONS

  • BA/BS Degree in a science or health-related discipline.
  • Comprehensive knowledge of the clinical research process and Good Clinical Practices from previous employment experience and/or education in the clinical research field.
  • Ability to integrate and summarize medical/scientific concepts in protocols and documents.
  • Experience participating in and/or co-leading an operational team.
  • Has working knowledge of statistics, data analysis, and data interpretation.
  • Exceptional written and oral communication and cross-functional collaborative skills.
  • Proficient in MS Word, Excel, and PowerPoint.

PREFERRED QUALIFICATION

  • Comprehensive knowledge of the clinical research process and Good Clinical Practices from previous employment experience and/or education in the clinical research field.
  • Ideally has working experience of vaccines therapeutic area.

Work Location Assignment: Hybrid

Purpose

Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.

Flexibility

We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self.

Equal Employment Opportunity

We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.

DisAbility Confident

We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!

Clinical Development Scientist - Vaccines, Manager in Milton Keynes employer: Pfizer

Pfizer is an exceptional employer that fosters a culture of innovation and inclusivity, making it an ideal place for Clinical Development Scientists to thrive. With a commitment to employee growth, flexible work arrangements, and a focus on breakthrough advancements in healthcare, Pfizer empowers its team members to make meaningful contributions to global vaccine development while enjoying a supportive and dynamic work environment.
Pfizer

Contact Detail:

Pfizer Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Development Scientist - Vaccines, Manager in Milton Keynes

✨Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field, especially those who work with vaccines. A friendly chat can lead to insider info about job openings or even a referral.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of Good Clinical Practices and the latest trends in vaccine development. We want you to shine when discussing your experience and how it aligns with the role!

✨Tip Number 3

Showcase your collaborative skills! Be ready to share examples of how you've worked effectively with cross-functional teams. This is key in a role that involves partnerships with various departments.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.

We think you need these skills to ace Clinical Development Scientist - Vaccines, Manager in Milton Keynes

Clinical Research Knowledge
Good Clinical Practices (GCP)
Protocol Development
Data Collection Tools Design
Clinical Data Review
Safety Oversight
Statistical Analysis
Data Interpretation
Written Communication Skills
Oral Communication Skills
Cross-Functional Collaboration
MS Word Proficiency
MS Excel Proficiency
MS PowerPoint Proficiency
Operational Team Leadership

Some tips for your application 🫡

Know Your Stuff: Make sure you brush up on your clinical research knowledge, especially around vaccines. We want to see that you’re not just ticking boxes but genuinely understand the science behind what we do.

Tailor Your Application: Don’t just send a generic CV and cover letter. We love it when applicants customise their documents to reflect how their experience aligns with our role. Show us why you’re the perfect fit for the Clinical Development Scientist position!

Be Clear and Concise: When writing your application, keep it straightforward. We appreciate clarity and brevity, so make sure your points are easy to read and get straight to the heart of your experience and skills.

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 and helps us keep track of all the amazing talent out there!

How to prepare for a job interview at Pfizer

✨Know Your Science

Make sure you brush up on the latest developments in vaccine research and clinical practices. Being able to discuss recent studies or breakthroughs will show your passion and knowledge in the field, which is crucial for a Clinical Development Scientist role.

✨Prepare for Scenario Questions

Expect questions that ask how you would handle specific situations, like protocol deviations or data discrepancies. Think of examples from your past experience where you successfully navigated similar challenges, as this will demonstrate your problem-solving skills.

✨Showcase Collaboration Skills

Since this role involves working closely with various teams, be ready to discuss your experience in cross-functional collaboration. Highlight instances where you effectively communicated with clinical operations, data management, or external partners to achieve study goals.

✨Familiarise Yourself with Regulatory Standards

Understanding Good Clinical Practices and relevant regulations is key. Be prepared to discuss how you've applied these standards in your previous roles, and think about how you can contribute to maintaining compliance and quality in clinical studies.

Clinical Development Scientist - Vaccines, Manager in Milton Keynes
Pfizer
Location: Milton Keynes

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