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...position is closely aligned with internal teams and is responsible for communicating both the scientific and operational benefits of Medpace services to prospective clients.
Responsibilities
* Work collaboratively with assigned Business Development Executives;
*...
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...Job Summary
Are you looking to work in a fast-paced environment? Come join he Medpace Shared Services team. We are seeking a candidate that can multi-task, is very detailed focused, and thrives in a team atmosphere. This position is responsible for the processing and...
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...functioning knowledge of and experience with Microsoft Office programs is required; and
* Excellent oral and written communication skills.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development...
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...Exemplary organizational skills
* Strong written and verbal communication skills; and
* Knowledge of MS Office (Excel and Outlook)
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development...
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...strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical...
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...with the project team to develop solutions;
* Maintain close collaboration, interaction, and effective working relationships with Medpace functional area colleagues;
* Attend clinical operations internal meetings as the Regulatory Affairs representative; and
*...
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...skills;
* Knowledge of Microsoft Office; and,
* Great attention to detail and excellent oral and written communication skills.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development...
Suggested
Full time
Contract work
Local area
Work from home
Flexible hours
Job Summary
Medpace is a leading CRO for Biotech companies and we are currently seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to...
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...Job Summary
Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team!
This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate...
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...Job Summary
Medpace is the leading CRO for Biotech companies and is continuing to add senior-level Directors and established Project Managers to join our Clinical Trial Management Group in Cincinnati, OH, or remotely with relevant experience. Our therapeutic areas of...
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...collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. We currently have openings at the experienced coordinator level. If you want an exciting career where you build upon the...
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...Compensation
A target salary range of $80,000-$120,000/year. Your compensation will be based on your skills and experience. Medpace offers the following benefits for eligible positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work...
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...Exceptionally strong communication skills; and
* Advanced knowledge of Microsoft Word, Excel, and PowerPoint.
Travel: minimal
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development...
Suggested
Remote job
Full time
Contract work
Local area
Work from home
Relocation bonus
Flexible hours
...Job Summary
Medpace is the leading CRO for Biotech companies and is continuing to add established Project Managers to join our Clinical Trial Management Group in Denver, CO. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic, Infectious...
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Job Summary
Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our...
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