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Job Details

Clinical Trial Manager - Device (Project Manager)

Company: Medpace
Location: Blaine
Reference: 2018-3323
Closing Date: 14 Mar 18
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team! Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Project Manager to join our Medical Device team. ...

Requirements:

Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team!



Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Project Manager to join our Medical Device team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.



* Lead clinical team providing daily work direction to clinical study team members to support needs of clinical site, and work to meet goals and timelines of Sponsor, including determining study objectives, strategy, scope, and schedule to meet Sponsor’s needs;
* Coordinate and manage project start-up, project maintenance, and project close-out activities;
* Maintain ongoing Sponsor contact for project-specific issues by serving as primary contact for Sponsor and all project team members;
* Monitor and drive study progress and identify and anticipate potential issues or challenges, and work with team to develop appropriate solutions;
* Provide management oversight of Clinical Study Associates, Clinical Trial Assistants, Clinical Research Associates and other clinical study team members;
* Develop Clinical Investigational Plans, Case Report Forms, Data Management Plans, Monitoring Plans, and other study-specific documents –and management tools;
* Lead regulatory submission and safety activities;
* Responsible for forecasting and budgeting for clinical study, and communicating change in scope to Sponsor clinical team and Medpace Account Manager;
* Interacting with and advise medical personnel;
* Conduct Qualification, Site Initiation, Routine Monitoring, and Study Site Close Out visits, as needed; and
* May be responsible for other projects and responsibilities as assigned.



* Bachelor’s degree in Life Sciences or related field and 3 years of related medical device industry experience (e.g., clinical monitoring or project management), or Master’s degree in Life Sciences or related field and 2 years related medical device industry experience (e.g., clinical monitoring or project management);
* Exceptional communication skills (oral and written);
* High attention to detail and quality standard;
* Strong time and project management skills;
* Strong customer service focus;
* Demonstrate appropriate judgment in making decisions/seeking supervisor support;
* Provide project-specific oversight of Clinical Study Associates, Clinical Trial Assistants, Clinical Research Associates and other team members;
* Demonstrate measurable knowledge of Good Clinical Practice for medical device trials in the US (21 CFR 812 and other sections) and/or Europe (ISO 14155), and local regulations; and
* Proficient with all Microsoft Office applications (Word, Excel, Power Point, Project, etc.).



WHY MEDPACE?



At Medpace, you will find work that is both challenging and rewarding. At Medpace, you will be given the tools and training to succeed. At Medpace, you will be rewarded for strong performance and provided opportunities to grow professionally.



WHAT TO EXPECT NEXT



We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an interview.



EO/AA Employer M/F/Disability/Vets



WHY MEDPACE?

At Medpace, you will find work that is both challenging and rewarding. At Medpace, you will be given the tools and training to succeed. At Medpace, you will be rewarded for strong performance and provided opportunities to grow professionally.



AWARDS

Medpace is being recognized locally, nationally, and globally for their work in the industry as well as the culture they have developed for their team.

* Medpace Named a Top Cincinnati Workplace for 2015, 2016 and 2017 by the Cincinnati Enquirer
* Medpace named Top Ten CRO in 2015 CenterWatch Investigative Site Survey
* Eagle Award winner and nominee – which recognizes outstanding leadership, professionalism, integrity, and dedication to advancing the clinical research profession through strong site partnerships.



WHAT TO EXPECT NEXT

We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an interview.



EO/AA Employer M/F/Disability/Vets

Apply for this job: Clinical Trial Manager - Device (Project Manager)

Contact Information:

Address:  Medpace, Inc
5375 Medpace Way
Cincinnati
Ohio
45227
USA
Tel:  +1 513 579 9911
Fax:  +1 513 579 0444
Website:  Visit Our Web Site

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