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Job Details

Contract Specialist, Study Start Up

Company: Medpace
Location: Prague
Reference: 2016-2493
Closing Date: 09 Dec 16
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, USA and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team! Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Contract Specialist to join our Clinical Operations 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, USA and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team!



Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Contract Specialist to join our Clinical Operations 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.



Ours is a culture of expertise, and we empower our teams to employ their unique talents and experience to take an assertive approach to research, problem solving, and ultimately supporting our partners. At Medpace our employees embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return they are rewarded with interesting projects, career advancement, and recognition and exposure to our international footprint. These are just a few reasons talented individuals join the Medpace team.



DESCRIPTION OF JOB DUTIES
•Negotiate contracts and budgets within pre-set parameters;
•Prepare original site and vendor contracts;
•Work with Medpace clinical trial team to manage the maintenance of study contracts;
•Ensure timelines are met in an efficient manner; and
•Act as a liaison between Sponsor, sites, vendors, and Medpace team.



QUALIFICATIONS/REQUIREMENTS
•Bachelor’s degree
•At least 1 year of experience, preferably in a clinical research setting;
•Demonstrated knowledge of the preparation and maintenance of contracts and budgets; and
•Proficient knowledge of Microsoft Word, Excel, and Outlook;
•Excellent time management skills;
•Excellent oral and written communication skills;
•Fluency in English and local language.



WHY MEDPACE?
Join Medpace, a mid-size global CRO that is growing and offers limitless opportunities in career growth and where you will be rewarded for strong performance. At Medpace, you will find work that is both challenging and rewarding and you will be given the tools and training to succeed.



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: Contract Specialist, Study Start Up

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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