Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Manage clinical trials, ensuring quality and compliance while collaborating with diverse teams.
- Company: Join AstraZeneca, a leader in innovative healthcare solutions.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real difference in healthcare by managing impactful clinical studies.
- Qualifications: Bachelor’s degree in a relevant field and 3-4 years of clinical trial experience.
- Other info: Diverse and inclusive workplace committed to equality and innovation.
The predicted salary is between 36000 - 60000 £ per year.
Global Study Manager
Duration – 12 months (interim)
Location – Remote
Inside IR35
The Global Study Manager is responsible for supporting the delivery of clinical studies ensuring quality and compliance. The exact accountabilities will differ depending on the exact nature of the clinical program, so a high degree of flexibility is required.
Responsibilities
Contribute to the development of study documents as appropriate as well as any updates/amendments, ensuring template and version compliance.
Lead the preparation of country specific agreements, confidentiality agreements, clinical trial applications and other applicable country documents.
Manage the set‐up of third‐party vendors assessing initial statement of work and budget, as well as the change order process.
Provide input to data management documents (e.g. Case Report Form, Data Validation Specifications), and interface with data management representatives and sites to facilitate the delivery of study data.
Initiate contract/budget requests and track ongoing status; facilitate generation of purchase orders, review vendor invoices and assist in tracking spend against approved budget.
Ensure the supply of Investigational product and study materials by liaising with Drug Supply or external service providers as appropriate.
Oversight of third party vendors, global / local internal staff and investigator sites to support effective delivery of a study and its regulatory documents from development of the protocol through to the Clinical Study Report.
Provide oversight of and support recruitment and data delivery as well as risk mitigation strategies.
Assist in the clinical trial insurance process; track approvals, revisions and renewals of certificates.
Monitor study conduct and progress, proactively identifying and resolving issues which may impact delivery of the study to the necessary quality, timelines or budget.
Support risk management and quality efforts to ensure study compliance.
Support set‐up, maintenance, closeout and archiving of the Trial Master File (TMF), ensuring continual inspection readiness.
Prepare presentation material for meetings, newsletters and websites.
Support the study team in the implementation of audits and regulatory inspections.
Contribute to review of new/amended/unique SOPs and guidance documents.
Qualifications
University degree / Bachelor\’s degree, preferably in medical or biological science, or discipline associated with Clinical Research, or equivalent experience
Minimum of 3‐4 years of progressive clinical trial experience
Experience of working with and delivering through strategic partners and 3rd party vendors
Excellent knowledge of ICH‐GCP principles
Demonstrated verbal and written communication skills
Early Phase experience (phase I and IIa)
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, colour, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status.
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry‐leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non‐discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements
#J-18808-Ljbffr
Clinical Trial Manager employer: AstraZeneca
Contact Detail:
AstraZeneca Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the hunt for a Clinical Trial Manager role. You never know who might have the inside scoop on an opportunity or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your ICH-GCP knowledge and be ready to discuss your experience with third-party vendors. We want to see how you can contribute to our team, so think of examples that showcase your skills and flexibility in managing clinical studies.
✨Tip Number 3
Don’t just apply anywhere; focus on roles that excite you! Use our website to find positions that match your skills and interests. Tailor your approach to each application, highlighting how your background aligns with the specific needs of the role.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Share any additional thoughts you have about the role or the company, and reiterate your enthusiasm for joining the team.
We think you need these skills to ace Clinical Trial Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trial Manager role. Highlight relevant experience and skills that match the job description, especially your knowledge of ICH-GCP principles and clinical trial processes.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for the role. Mention specific experiences that demonstrate your ability to manage clinical studies and work with third-party vendors.
Showcase Your Flexibility: Since the role requires a high degree of flexibility, make sure to mention instances where you've adapted to changing circumstances in previous roles. This will show us that you can handle the dynamic nature of clinical trials.
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 any important updates from us!
How to prepare for a job interview at AstraZeneca
✨Know Your Clinical Trials
Make sure you brush up on your knowledge of clinical trials, especially phases I and IIa. Be ready to discuss your previous experiences and how they relate to the responsibilities outlined in the job description. This shows that you understand the role and can hit the ground running.
✨Familiarise Yourself with Compliance Standards
Since the role involves ensuring quality and compliance, it’s crucial to be well-versed in ICH-GCP principles. Prepare examples of how you've maintained compliance in past projects, as this will demonstrate your commitment to quality and regulatory standards.
✨Prepare for Vendor Management Questions
Given the emphasis on managing third-party vendors, think about your experiences working with strategic partners. Be ready to discuss how you’ve assessed statements of work, managed budgets, and navigated change orders. This will highlight your ability to handle vendor relationships effectively.
✨Showcase Your Communication Skills
As communication is key in this role, prepare to demonstrate your verbal and written skills. Bring examples of presentation materials or reports you've created in the past. This will help illustrate your ability to convey complex information clearly and effectively.
