At a Glance
- Tasks: Lead clinical trials in Oncology, Cardiovascular, Metabolic, or GI fields with accountability and oversight.
- Company: Join Medpace, a top CRO for Biotech companies, in a dynamic London team.
- Benefits: Enjoy flexible work, competitive pay, bonuses, equity grants, and generous PTO.
- Other info: Structured career paths and employee wellness initiatives to support your growth.
- Why this job: Make a real impact in healthcare while advancing your career in a supportive environment.
- Qualifications: Bachelor's degree in health/life sciences and 5+ years of clinical trial management experience.
The predicted salary is between 60000 - 80000 € per year.
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Clinical Trial Managers with expertise in Oncology / Cardiovascular / Metabolic / GastroIntestinal indications are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. We provide remote flexibility only with relevant experience. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.
Responsibilities
- Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations.
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables.
- Maintain in depth knowledge of protocol, therapeutic area, and indication.
- Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided.
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable.
- Develop operational project plans.
- Manage risk assessment and execution.
- Responsible for management of study vendor.
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.
Qualifications
- Bachelor's degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred.
- Experience in Phases 1-4; Phases 2-3 preferred.
- Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred.
- Management of overall project timeline.
- Bid defense experience preferred.
- Strong leadership skills.
Benefits
- Flexible work environment.
- Competitive compensation and benefits package.
- Competitive PTO packages.
- Structured career paths with opportunities for professional growth.
- Company-sponsored employee appreciation events.
- Employee health and wellness initiatives.
Experienced Clinical Trial Manager (Oncology / Cardiovascular / Metabolic / GI) in London employer: Medpace, Inc.
Medpace is an exceptional employer for Clinical Trial Managers, offering a dynamic work environment in London that fosters professional growth and development. With a competitive salary and benefits package, including equity grants, employees enjoy a flexible work culture that prioritises health and wellness, alongside structured career paths and regular appreciation events to celebrate achievements.
StudySmarter Expert Advice🤫
We think this is how you could land Experienced Clinical Trial Manager (Oncology / Cardiovascular / Metabolic / GI) in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical trial space, especially those who work at Medpace or similar companies. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH/GCP guidelines and the specific therapeutic areas you're interested in. We want you to shine when discussing your experience and how it aligns with the role!
✨Tip Number 3
Showcase your leadership skills! Be ready to share examples of how you've managed teams and projects in the past. We love hearing about your successes and how you’ve tackled challenges head-on.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always on the lookout for passionate Clinical Trial Managers like you to join our team.
We think you need these skills to ace Experienced Clinical Trial Manager (Oncology / Cardiovascular / Metabolic / GI) in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to highlight your experience in Clinical Trial Management, especially in Oncology, Cardiovascular, Metabolic, or GI. We want to see how your skills match the job description, so don’t be shy about showcasing relevant projects you've managed.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your background makes you a perfect fit. We love seeing enthusiasm and a clear understanding of our work at Medpace.
Showcase Your Leadership Skills:Since strong leadership is key for this role, make sure to highlight any experiences where you've led teams or projects. We want to know how you’ve managed operations and driven success in your previous roles.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re serious about joining our team!
How to prepare for a job interview at Medpace, Inc.
✨Know Your Stuff
Make sure you have a solid understanding of the clinical trial phases, especially Phases 1-4. Brush up on your knowledge of oncology, cardiovascular, metabolic, and GI indications. This will not only help you answer questions confidently but also show that you're genuinely interested in the role.
✨Showcase Your Leadership Skills
As a Clinical Trial Manager, you'll need to demonstrate strong leadership abilities. Prepare examples from your past experiences where you've successfully led a team or managed a project. Highlight how you handled challenges and ensured project deliverables were met.
✨Familiarise Yourself with ICH/GCP Guidelines
Since compliance is key in clinical trials, make sure you're well-versed in ICH/GCP guidelines. Be ready to discuss how you've applied these regulations in your previous roles and how you ensure adherence within your teams.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's projects, culture, and future directions. This shows your enthusiasm for the role and helps you gauge if the company is the right fit for you. Plus, it demonstrates that you’re proactive and engaged.
