Director, Clinical Trial Manager NASH Experience Required

  • Anywhere

Company :

Location :
Cincinnati, Ohio

Expiry Date :
Fri, 06 Nov 2020 23:59:59 GMT

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Description :

Medpace is a full-service clinical contract research organization (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 approximately 3,500
people across almost 40 countries.


Medpace is seeking a Cincinnati, OH based Director, Clinical Trial Management
to act as project lead for multiservice full service global clinical trials.
The position interacts with sponsors and manages the timeline and all project
deliverables. Are you interested in delivering effective, end-to-end
collaboration, training, and resource planning around the globe to accelerate
the global development of safe and effective medical therapeutics? If so, this
opportunity is for you.

* 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

* Bachelor s degree in a health-related field; Advanced degree in a
health-related field preferred
* Experience in Phases 1-4; Phases 2-3 preferred
* 5+ years as a project/clinical trial manager within a CRO
* Management of overall project timeline
* Bid defense experience
* Strong leadership skills

Why Medpace?

When you join Medpace, you become part of a team dedicated to supporting the
development of ground-breaking drugs and devices. Our employees provide hope
for those living with debilitating diseases. We invite you to be a part of
something that is impacting millions of people around the globe while enjoying
a competitive total compensation and benefits package and internal growth

* Medpace historically named a Top Cincinnati Workplace by the Cincinnati
* Medpace ranks amongst top CROs for site ratings across all 10 important
attributes including CRA training, preparation & organization,
accessibility of staff, open communication, and ensuring timely drug
* Continually recognized with CRO Leadership Awards from Life Science
Leader magazine based on expertise, quality, capabilities, reliability,
and compatibility


A member of our recruitment team will review your qualifications and, if
interested, you will be contacted for an interview.

EO/AA Employer M/F/Disability/Vets

WARNING: Please beware of phishing scams that offer opportunities with Medpace
in exchange for sending money. These scammers pose as legitimate employees from
actual companies. Please be advised that a Medpace employee will never ask you
for a credit card, send you a check, or ask you for any type of payment as part
of consideration for a role with our company. All of our careers require that
you first complete an online application and go through some sort of interview


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