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- Tasks: Lead scientific project delivery and coordinate with experts in clinical research.
- Company: Emerald Clinical Trials, a global leader in clinical research.
- Benefits: Competitive salary, flexible working, career growth, and wellbeing initiatives.
- Why this job: Make a real impact on global health through innovative clinical trials.
- Qualifications: Degree in life sciences and experience in clinical research required.
- Other info: Join a diverse team dedicated to improving lives worldwide.
The predicted salary is between 36000 - 60000 ÂŁ per year.
At Emerald Clinical Trials, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post‑marketing. Our therapeutic expertise spans renal, cardiometabolic, and oncology, areas where we make a significant impact on improving global health. At the heart of our success is our ability to combine global reach with local knowledge. Our on‑the‑ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results – bringing therapies to patients in need.
About the Role
We are seeking a Project Manager, Scientific Leadership, home‑based in the EU, to support the delivery and coordination of our Scientific Leadership services across global studies. This unique role sits at the intersection of science, operations, and strategic project delivery. You will work closely with Key Opinion Leaders (KOLs), Scientific Leads, and internal teams to implement scientific advisory activities that shape study design and execution. You’ll also coordinate the operational aspects of steering committees, endpoint adjudication, and other scientific governance bodies throughout the clinical trial lifecycle.
Your Responsibilities
- Lead and manage operational delivery of scientific leadership components within assigned projects
- Serve as key liaison for Regional and National Scientific Leads
- Coordinate communications, meetings, contracting, and payments related to scientific committees and advisors
- Maintain real‑time project trackers, metrics, and reporting documents
- Collaborate cross‑functionally to ensure scientific governance is integrated smoothly into project execution
- Contribute to client deliverables, including progress reports and strategy presentations
- Support continuous improvement of scientific leadership processes and templates
- Ensure compliance with SOPs, ICH‑GCP, and regulatory requirements
- Provide backup support to the Project Lead as needed
- Support knowledge sharing and team development within the organisation
About You
- Bachelor’s degree in a life sciences, health, or related discipline
- Experience liaising with scientific or medical professionals, including KOLs or investigators
- Strong understanding of clinical research processes, scientific governance, and stakeholder engagement
- Familiarity with ICH‑GCP and clinical trial regulations
- Excellent communication, organisational, and project management skills
- Able to manage multiple priorities in a fast‑paced environment
- Fluent in written and spoken English
- Tech‑savvy with proficiency in Microsoft Office and virtual collaboration tools
- Extensive experience in clinical research, preferably within a CRO or academic setting
Why Join Us?
At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide. Here’s what makes us stand out:
- Purpose‑Driven Work: You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.
- Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial.
- Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.
What We Offer
We understand that great work happens when people feel valued and supported. That’s why we provide:
- Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience.
- Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role.
- Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.
- Employee Wellbeing: Participate in programs and initiatives designed to promote work‑life balance, health, and team connection, including global engagement surveys, recognition programs, and team‑building events.
- Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients.
Equal Opportunity Statement
We are an equal‑opportunity employer and encourage applications from all qualified candidates.
Senior Project Manager, Scientific Leadership and Medical Affairs employer: Emerald Clinical Trials Inc.
Contact Detail:
Emerald Clinical Trials Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Project Manager, Scientific Leadership and Medical Affairs
✨Tip Number 1
Network like a pro! Reach out to professionals in the industry, especially those who work at Emerald Clinical Trials. Use LinkedIn to connect and engage with them; you never know who might help you land that interview!
✨Tip Number 2
Prepare for your interviews by researching the company and its projects. Familiarise yourself with their therapeutic areas like renal, cardiometabolic, and oncology. This shows you're genuinely interested and ready to contribute to their mission.
✨Tip Number 3
Practice your communication skills! As a Project Manager, you'll need to liaise with various stakeholders. Mock interviews with friends or mentors can help you articulate your experience and how it aligns with the role.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining our team and contributing to meaningful clinical research.
We think you need these skills to ace Senior Project Manager, Scientific Leadership and Medical Affairs
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the Senior Project Manager role. Highlight your experience in clinical research and any relevant projects you've managed, especially those involving scientific governance.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're passionate about clinical research and how your background makes you a great fit for our team. Be sure to mention your experience with KOLs and your understanding of ICH-GCP guidelines.
Showcase Your Communication Skills: Since this role involves liaising with various stakeholders, demonstrate your excellent communication skills in your application. Use clear and concise language, and provide examples of how you've effectively communicated in past roles.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s the easiest way for us to keep track of your application and ensure it reaches the right people!
How to prepare for a job interview at Emerald Clinical Trials Inc.
✨Know Your Science
Brush up on your knowledge of clinical research processes and the specific therapeutic areas mentioned in the job description, like renal, cardiometabolic, and oncology. Be prepared to discuss how your scientific expertise can contribute to the projects at Emerald Clinical Trials.
✨Showcase Your Project Management Skills
Highlight your experience in managing multiple priorities and delivering projects on time. Use specific examples from your past roles to demonstrate your organisational skills and ability to coordinate with various stakeholders, especially KOLs and scientific leads.
✨Familiarise Yourself with Regulations
Make sure you understand ICH-GCP guidelines and other regulatory requirements relevant to clinical trials. Being able to discuss compliance confidently will show that you are serious about maintaining high standards in scientific governance.
✨Engage with the Interviewers
Prepare thoughtful questions that reflect your interest in the role and the company’s mission. Engaging with the interviewers not only shows your enthusiasm but also helps you assess if the company culture aligns with your values.