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- Tasks: Join our webinar to explore Clinical Trial Manager roles and daily responsibilities at Medpace.
- Company: Medpace is a leading CRO dedicated to advancing medical therapeutics globally.
- Benefits: Enjoy flexible work, competitive pay, career growth, and wellness initiatives.
- Why this job: Make a real impact on patient lives while working in a supportive and innovative environment.
- Qualifications: 5+ years in Clinical Trial Management; a degree in health or life sciences is preferred.
- Other info: This anonymised event allows you to learn without revealing your identity.
The predicted salary is between 36000 - 60000 £ per year.
Experienced in Clinical Operations considering a move to a stable and rapidly growing CRO? Medpace is delighted to host an anonymised online webinar event tailored for experienced Clinical Operations Project Managers / Clinical Trial Managers in the industry to inform you about the Clinical Trial Manager and Associate Director positions at Medpace. This is a rare and exciting opportunity for experienced CTM's to gain an insight into what life is like working as a Clinical Trial Manager at Medpace, what differentiates us from our competitors, the defined career path, competitive benefits we offer and an anonymised Q&A session via the chat function.
Join the Medpace hiring team via this online webinar for an exclusive, anonymised event to hear from our Clinical Trial Management leadership team in Europe. This event can act as a first step in the hiring process for an eventual CTM and Associate Director positions (we are open to consider varying levels of seniority), or this may be an informative session for you to find out more about Medpace and the high quality service we offer in order to contribute to the drug development process and to help improve the lives of patients.
LOCATION: Online Webinar
DATE: Tuesday 15th July
APPLICATION CLOSE DATE: Friday 11th July
Please note this event will be anonymised - your name and face will not be visible to other registrants and presenters in the room.
What to Expect Next: A member of our recruitment team will review your CV, if interested, you will be contacted for an RSVP.
Responsibilities
- Manage and provide accountability for day-to-day operations of the studies conducted by Medpace on behalf of Biotech sponsors, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, SOPs 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.
- Lead internal project team and provide cross-functional oversight of study team deliverables.
- Review and provide input for study protocol, database edit check specifications and final study report, when applicable.
- Develop study-specific operational project plans.
- Implement and manage a risk-based approach to project execution.
- Responsible for management of study vendors.
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables, including CRA trip report review.
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.
- 5+ years of Project Manager/Clinical Trial Manager experience at a CRO required.
- Management of overall project timeline; Bid defense experience preferred.
- Strong leadership skills.
Medpace Overview
Medpace is a full-service clinical contract research organisation (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment.
- Competitive compensation and benefits package.
- Competitive annual leave packages.
- Structured career paths with opportunities for professional growth.
- Company-sponsored employee appreciation events.
- Employee health and wellness initiatives.
Awards
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024. Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets
Medpace: Clinical Trial Management (Europe) – Anonymised Webinar Event For Experienced CTM\'s employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medpace: Clinical Trial Management (Europe) – Anonymised Webinar Event For Experienced CTM\'s
✨Tip Number 1
Make sure to attend the anonymised webinar event on 15th July. This is a fantastic opportunity to hear directly from Medpace's Clinical Trial Management leadership team and gain insights into the company culture and expectations.
✨Tip Number 2
Prepare thoughtful questions for the Q&A session during the webinar. This shows your genuine interest in the role and helps you stand out as a candidate who is engaged and proactive.
✨Tip Number 3
Network with other attendees during the webinar. Building connections with fellow professionals can provide valuable insights and potentially lead to referrals or recommendations within the industry.
✨Tip Number 4
After the webinar, follow up with a thank-you email to the recruitment team at Medpace. Express your appreciation for the event and reiterate your interest in the Clinical Trial Manager position, which can leave a positive impression.
We think you need these skills to ace Medpace: Clinical Trial Management (Europe) – Anonymised Webinar Event For Experienced CTM\'s
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and qualifications required for the Clinical Trial Manager position. Tailor your application to highlight relevant experience in clinical operations and project management.
Craft a Strong CV: Your CV should clearly outline your experience in Clinical Trial Management, including specific projects you've managed, your role in those projects, and any relevant achievements. Use quantifiable metrics where possible to demonstrate your impact.
Write a Compelling Cover Letter: In your cover letter, express your enthusiasm for the role and Medpace as a company. Highlight your understanding of their mission and how your background aligns with their goals. Be sure to mention your experience in Phases 1-4 and any leadership roles you've held.
Prepare for the Webinar: Since this is an anonymised webinar event, prepare questions in advance that you would like to ask about the role or the company. This shows your interest and can help you stand out when you follow up after the event.
How to prepare for a job interview at Medpace
✨Know Your Stuff
Make sure you have a solid understanding of clinical trial management and the specific phases involved. Familiarise yourself with Medpace's operations, their therapeutic areas, and how they differentiate themselves from competitors.
✨Prepare for the Q&A
Since this is an anonymised webinar, prepare thoughtful questions to ask during the Q&A session. This shows your interest in the role and helps you gather valuable insights about the company culture and expectations.
✨Highlight Relevant Experience
Be ready to discuss your previous experience in clinical operations, especially any roles that involved managing projects or teams. Use specific examples to demonstrate your leadership skills and ability to handle challenges.
✨Show Enthusiasm for the Role
Express genuine enthusiasm for the Clinical Trial Manager position and the impact it has on patient lives. Companies like Medpace value candidates who are passionate about their mission and the work they do.