At a Glance
- Tasks: Support clinical trials by managing documentation, vendor oversight, and ensuring timely study updates.
- Company: Leading multinational Biotech company based in London.
- Benefits: Gain valuable experience in a dynamic industry with potential for career growth.
- Other info: Join a collaborative team focused on delivering high-quality data for clinical development.
- Why this job: Make a real impact in healthcare by contributing to innovative clinical studies.
- Qualifications: BS in nursing, life or health sciences preferred; relevant experience considered.
The predicted salary is between 40000 - 50000 £ per year.
PE Global is currently recruiting for a Study Specialist for an initial 12 month contract role with a leading multinational Biotech client based in London. The Global Study Operations organization is tasked with providing strategic direction on the feasibility, design, and conduct of Phase 1-4 and post approval studies and drives the delivery of high-quality data to support the registration approval and post approval activities of our clinical development assets. The organization achieves this through the development and operationalization of Clinical Development Plans, study planning and delivery, cross-functional leadership of Study Execution Teams, operational trial expertise, and vendor management and oversight.
Activities and responsibilities may include:
- Develop and/or review study specific documentation, as delegated by the Study Manager
- Contribute to the management of country and site feasibility assessment
- Provide support in the management of Regulatory document collection and tracking (in the absence of a CRO) for participating sites
- Contribute to the collection and oversight of essential documents for study life-cycle management
- Contribute to the development of site and investigator training materials
- May present at investigator meetings as assigned
- Ensure timely study entry and updates to ClinicalTrials.gov
- Ensure investigator payment: site set-up, pass-through processing, visit payment processing and funding processing (in collaboration with payment vendor)
- Provide administrative assistance with internal and external meetings including investigator meeting(s) as warranted
- Facilitate Screening Authorization Forms tracking/sign off where applicable
- Manage various Global Study Operations document translations as applicable
- Process documents for signature in DocuSign
- Site management for delegated site(s)
- Manage and resolve site related issues and risks escalated to BioMarin that can’t be resolved by CRO
- Contribute to identifying risks identification and mitigations
- Oversee the Clinical Trial Insurance process
- Support Study Manager to ensure timely delivery and handling of IP to the sites
- Support Vendor Management
- Attend internal Global Study Operations team meetings, vendor meetings, and/or Cross-Function Study Execution Meeting(s) as GSO representative and take meeting minutes as requested
- Oversee and manage essential documents in the Trial Master File (TMF)
- Contribute to Global Study Operations risks identification and mitigations
- Provide support and administrative assistance with internal and external meetings
- Assist with filing GSO internal study documents in internal systems
Requirements:
- BS or higher in nursing, life or health sciences is preferred
- Industry or relevant experience in lieu of education may be considered
- Experience in oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.)
Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK.
Clinical Trial Specialist in Slough employer: PE Global
PE Global is an exceptional employer, offering a dynamic work environment in the heart of London, where innovation meets collaboration. As a Clinical Trial Specialist, you will benefit from a culture that prioritises employee growth through continuous learning opportunities and cross-functional teamwork, all while contributing to impactful clinical studies that advance healthcare. With a commitment to high-quality data delivery and operational excellence, PE Global empowers its employees to thrive in their roles and make a meaningful difference in the biotech industry.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Trial Specialist in Slough
✨Join Biotechnology Meetups
Get yourself into the loop by joining local biotech meetups or workshops. These events are perfect for making connections with professionals in the field and can often lead to temporary gigs through word-of-mouth. Plus, you'll get to hear about the latest trends and developments directly from the source.
✨Showcase Your Passion in Science
Consider starting a blog or social media channel to showcase your interest in biotechnology. Share the latest research, your insights, and even your projects. This will not only enhance your visibility in the community but also attract potential employers like PE Global who might be scrolling through for talent.
✨Tap into University Resources
If you’re still in school or recently graduated, don’t forget to use your university’s career services. They often have exclusive connections with companies looking for temporary staff. Reach out to them for internship listings and networking opportunities tailored to the biotech sector.
✨Apply Directly on Our Website
When you spot that perfect temporary role at PE Global, make sure to apply directly through our website. This way, you’ll be in the best position to get noticed quickly and can show your enthusiasm for the role while filling out the application.
We think you need these skills to ace Clinical Trial Specialist in Slough
Some tips for your application 🫡
Showcase Relevant Lab Skills:In the biotech world, your lab skills are paramount. Make sure your CV highlights specific techniques and equipment you’ve used, such as PCR, gel electrophoresis, or cell culture. This will give us a clear picture of what you can bring to PE Global as a temporary teammate.
Highlight Your Research Experience:If you’ve worked on any research projects — whether during your studies or in previous positions — make sure to detail these in your application. Include the objective, your role, and what you achieved. This will help us see your potential and fit for the temporary position at PE Global.
Keep It Concise and Relevant:Especially for a temporary role, we want to see a clear and focused application. Tailor your CV and cover letter to emphasise the qualifications and experiences that are most relevant to the biotech field and the specific role at PE Global. This shows us you’re genuinely interested and capable.
Be Clear About Your Availability:Since it’s a temporary role, let us know right away when you’re available to start and how long you can commit. Include this in your cover letter — this kind of transparency saves us all time and helps us find the right fit quickly at PE Global.
How to prepare for a job interview at PE Global
✨Brush Up on Your Biotech Basics
Understanding the fundamental concepts in biotechnology is crucial. Be ready to discuss core topics like genetics, molecular biology, or bioinformatics, especially if you're asked technical questions. We suggest revisiting your coursework or recent projects to refresh your memory.
✨Demonstrate Your Adaptability
Since this is a temporary role, they’re likely looking for someone who can jump in and get up to speed quickly. Share experiences where you’ve adapted to new environments, tools, or teams in a short space of time. It shows you're ready to tackle the challenge head-on!
✨Emphasise Your Lab Experience
If you’ve got hands-on experience in lab settings, now’s the time to showcase it. Talk about specific techniques you’ve mastered, like PCR or chromatography, and any relevant safety protocols you’ve followed. These details help paint you as an effective team member from day one.
✨Be Prepared to Explain Your Passion
Hiring managers want to see your motivation, especially for a temporary position in a fast-paced field like biotechnology. Be ready to discuss what excites you about the industry, your career goals, and how this role at PE Global aligns with them. It’s all about showing that you’re not just looking for a job, but a stepping stone in your biotech journey.
