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 h ear 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
Clinical Trial Manager:
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 vendor s
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; and
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
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; and
Strong leadership skills.
Clinical Trial Manager:
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 vendor s
Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables, including CRA trip report review
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