Senior Study Specialist in England
Senior Study Specialist

Senior Study Specialist in England

England Temporary 68000 - 85000 £ / year (est.) Home office (partial)
Go Premium
P

At a Glance

  • Tasks: Oversee clinical trials and manage site/vendor relationships for impactful research.
  • Company: Join a leading biopharmaceutical company in London with a hybrid work model.
  • Benefits: Competitive daily rate, potential for full-time conversion, and flexible working environment.
  • Why this job: Make a difference in clinical research while developing your leadership skills.
  • Qualifications: 3-5 years in clinical research with strong communication and project management skills.
  • Other info: Opportunity for career growth in a dynamic and supportive team.

The predicted salary is between 68000 - 85000 £ per year.

PE Global is recruiting a Senior Study Specialist for our biopharmaceutical client based in London. The rate for this role is £340 per day Umbrella.

Location: Hybrid – 2 days/week in Holborn office (Wednesday + one additional day). Start Date: Ideally early November.

About the Role

We are seeking a Senior Study Specialist to join our clients Global Study Operations (GSO) team, supporting the execution and oversight of clinical trials. This is a hybrid contract position created as a backfill for a contractor converting to a full-time employee. The role has strong potential for extension and future full‑time conversion, depending on business needs. You will play a key role in site and vendor management, contributing to activities that directly impact participant safety, data integrity, timelines, and study quality. This position requires a high level of independence, leadership, and communication, as well as the ability to handle complex vendors, sites, and regional oversight.

Key Responsibilities

  • Oversight of site monitoring and management activities
  • Management of study vendors and related issue escalations
  • Support and execution of study documentation and operational plans
  • Lead or contribute to activities delegated by Study Manager or Program Lead
  • Maintain strong relationships with CROs and Key Principal Investigators
  • Provide support or coverage for Study Manager as needed

What We’re Looking For

  • 3–5 years’ experience in clinical research, ideally with regional lead experience in a sponsor or CRO setting
  • Proven ability to work autonomously and lead complex tasks or projects
  • Proficiency with systems such as Veeva, RAVE, eCOA, IRT, CTMS
  • Strong interpersonal skills with a collaborative, proactive, and adaptable mindset
  • Biopharmaceutical industry experience required

Please note PE Global is unable to provide candidates with visa sponsorship. Candidates will need the full right to live and work full time within the UK for at least the next 24 months.

Seniority level: Not Applicable

Employment type: Contract

Job function: Science, Research, and Other

Industries: Pharmaceutical Manufacturing and Biotechnology Research

Senior Study Specialist in England employer: PE Global

PE Global is an exceptional employer, offering a dynamic work environment in the heart of London, where innovation meets collaboration. With a strong focus on employee growth and development, our hybrid work model allows for flexibility while fostering a culture of teamwork and excellence in clinical research. Join us to make a meaningful impact in the biopharmaceutical industry, with opportunities for contract extension and potential full-time conversion.
P

Contact Detail:

PE Global Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Study Specialist in England

✨Tip Number 1

Network like a pro! Reach out to your connections in the biopharmaceutical industry and let them know you're on the lookout for opportunities. A friendly chat can sometimes lead to job openings that aren't even advertised.

✨Tip Number 2

Prepare for interviews by researching the company and its recent projects. Show them you’re not just another candidate; you’re genuinely interested in their work and how you can contribute to their clinical trials.

✨Tip Number 3

Practice your answers to common interview questions, especially those related to site management and vendor oversight. We want you to feel confident and ready to showcase your experience in clinical research!

✨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, we love seeing familiar faces from our community!

We think you need these skills to ace Senior Study Specialist in England

Clinical Research
Site Management
Vendor Management
Study Documentation
Operational Planning
Leadership
Communication Skills
Interpersonal Skills
Proficiency with Veeva
Proficiency with RAVE
Proficiency with eCOA
Proficiency with IRT
Proficiency with CTMS
Adaptability
Collaboration

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Senior Study Specialist role. Highlight your experience in clinical research and any relevant systems you've worked with, like Veeva or CTMS. We want to see how your skills match what we're looking for!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for our Global Study Operations team. Share specific examples of your leadership and project management experience that align with the job description.

Showcase Your Interpersonal Skills: Since this role requires strong interpersonal skills, don’t forget to mention your collaborative mindset and adaptability. We love candidates who can build relationships with CROs and Principal Investigators, so give us some examples!

Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!

How to prepare for a job interview at PE Global

✨Know Your Stuff

Make sure you brush up on your clinical research knowledge, especially around biopharmaceuticals. Familiarise yourself with key terms and processes related to site monitoring, vendor management, and study documentation. This will help you speak confidently about your experience and how it aligns with the role.

✨Showcase Your Independence

Since the role requires a high level of autonomy, be ready to share examples of how you've successfully led complex tasks or projects in the past. Highlight situations where you took initiative and managed challenges independently, as this will demonstrate your capability to thrive in this position.

✨Build Rapport

Strong interpersonal skills are crucial for this role. During the interview, focus on building a connection with your interviewers. Use active listening, maintain eye contact, and engage in a friendly manner. This will show that you can foster strong relationships with CROs and Principal Investigators, which is key for the job.

✨Be Ready for Scenarios

Prepare for situational questions that may test your problem-solving skills. Think of specific scenarios where you had to manage issues with vendors or sites, and how you resolved them. This will not only showcase your experience but also your proactive and adaptable mindset, which is exactly what they’re looking for.

Senior Study Specialist in England
PE Global
Location: England
Go Premium

Land your dream job quicker with Premium

You’re marked as a top applicant with our partner companies
Individual CV and cover letter feedback including tailoring to specific job roles
Be among the first applications for new jobs with our AI application
1:1 support and career advice from our career coaches
Go Premium

Money-back if you don't land a job in 6-months

P
  • Senior Study Specialist in England

    England
    Temporary
    68000 - 85000 £ / year (est.)
  • P

    PE Global

Similar positions in other companies
UK’s top job board for Gen Z
discover-jobs-cta
Discover now
>