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- Tasks: Lead clinical operations, manage budgets, and oversee study consistency.
- Company: Join a global pharma leader dedicated to innovative healthcare solutions.
- Benefits: Enjoy a hybrid work model with potential for contract extension.
- Why this job: Make a real impact in clinical trials while collaborating with top professionals.
- Qualifications: Strong experience in global study management and knowledge of drug development regulations required.
- Other info: Opportunity to contribute to diverse disease areas and enhance your career.
The predicted salary is between 48000 - 72000 £ per year.
Global Pharma is recruiting Clinical Ops Leads
6 month initial contracts (with the expectation of extension) in scope and hybrid (Welwyn Garden City)
You will require Strong Clinical Global Study Management experience at this level.
Drive operation excellence by developing operational plans, creating and managing a clinical study budget and overseeing the consistency of operations
Manage Vendors and stakeholders
Manage Risk and Compliance
Provide oversight by leading feasibility assessments to ensure countries and sites are selected for participation in trials. Provide guidance to country operational reps during trials
Manage site level engagement and other important healthcare partners.
You will contribute to the delivery of the portfolio of clinical studies and programs across Disease Areas by providing operational and/or strategic input to the teams.
Contribute and enable innovative clinical trial delivery and address emergent, high-impact needs that arise
You will be a self-starter who finds passion in achieving successful outcomes and delivering during your assignment.
Possess strong working knowledge of the drug development process and respective regulations, including ICH and GCP guidelines
Please send your CV if this looks to be of interest, and we can discuss it further.
Claire Helliwell #4583288 – Claire Helliwell
Clinical Operations Lead employer: Hays
Contact Detail:
Hays Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Operations Lead
✨Tip Number 1
Make sure to highlight your experience in managing clinical studies and operational excellence. Use specific examples from your past roles to demonstrate how you've successfully developed operational plans and managed budgets.
✨Tip Number 2
Familiarize yourself with the latest trends and challenges in clinical operations. Being able to discuss current issues and innovative solutions during your interview will show that you're proactive and knowledgeable about the field.
✨Tip Number 3
Network with professionals in the clinical operations space, especially those who have worked with Global Pharma or similar organizations. This can provide you with valuable insights and potentially lead to referrals.
✨Tip Number 4
Prepare to discuss your experience with risk management and compliance in detail. Be ready to share how you've navigated challenges in these areas and ensured adherence to ICH and GCP guidelines in your previous roles.
We think you need these skills to ace Clinical Operations Lead
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Clinical Operations Lead position. Understand the key responsibilities and required skills, such as strong clinical global study management experience and knowledge of ICH and GCP guidelines.
Tailor Your CV: Customize your CV to highlight relevant experience in clinical operations, vendor management, and risk compliance. Use specific examples that demonstrate your ability to drive operational excellence and manage clinical study budgets.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical trial delivery and your self-starter attitude. Mention how your background aligns with the expectations outlined in the job description and express your enthusiasm for contributing to innovative clinical trial solutions.
Proofread and Submit: Before submitting your application, carefully proofread your CV and cover letter for any errors. Ensure that all information is accurate and that your documents are formatted professionally. Then, submit your application through our website.
How to prepare for a job interview at Hays
✨Showcase Your Clinical Study Management Experience
Be prepared to discuss your previous roles in clinical study management. Highlight specific projects where you drove operational excellence and managed budgets effectively.
✨Demonstrate Vendor and Stakeholder Management Skills
Share examples of how you've successfully managed vendors and engaged stakeholders in past projects. This will show your ability to maintain strong relationships and ensure smooth operations.
✨Discuss Risk and Compliance Strategies
Prepare to talk about your approach to managing risk and compliance in clinical trials. Provide insights into how you've led feasibility assessments and ensured adherence to regulations like ICH and GCP.
✨Emphasize Your Self-Starter Attitude
Convey your passion for achieving successful outcomes. Share instances where you took the initiative to solve problems or improve processes, demonstrating your proactive nature.
