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Job Details

Clinical Project Manager - Medical Device

Company: Medpace
Location: Blaine
Reference: 2017-3180
Closing Date: 05 Dec 17
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

POSITION 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 Project Manager to join our device team. ...

Requirements:

POSITION 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 Project Manager to join our 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.



DESCRIPTION OF JOB DUTIES

* Determine study objectives, strategy, scope, and schedule in order to meet the goals and timelines of the clinical study sponsor;
* Ensure consistent study execution through the development of supporting study documents such as Clinical Investigation Plans, Case Report Forms, Data Management Plans, and Monitoring Plans;
* Direct daily activities for the clinical study associates and other team members and monitor program metrics to ensure consistent and predictable study progress;
* Actively identify issues and challenges that present barriers to program success and develop and implement appropriate solutions;
* Forecast appropriate timelines for the clinical study;
* Conduct literature reviews to support regulatory filings; and
* Determine clinical trial strategies and prepare clinical trial protocols.



QUALIFICATIONS/REQUIREMENTS

* Bachelor’s degree in Life Sciences or a related field;
* At least 5 years of clinical study experience, including prior experience with medical device trials;
* Previous training/mentoring experience is preferred;
* Outstanding oral and written communication skills;
* Strong customer service focus and project management skills;
* Proven ability to work autonomously on complex projects where critical thinking and innovative solutions are required;
* High attention to detail and quality standard; and
* Proficient in Microsoft Office applications.



Travel: None



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

Apply for this job: Clinical Project Manager - Medical Device

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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