Advanced Degrees Virtual Recruitment Event - Dec. 13th Job at Medpace, Inc.
Job Summary:
If interested, please fill out an application below. We're excited to speak to you!
Clinical Research Associate (CRA)
Project Coordinator (PC in CRO)
Associate Clinical Trial Manager
Regulatory Submissions Coordinator (RSC)
Data Coordinator
Medical Writer/Regulatory Writer
Qualifications :
The work we’ve done over the past 30 years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Celebrates 30 Years
Awards:
What to Expect Next:
Calling all candidates with Advanced Degrees! Join us virtually on December 13th to learn about our available positions in Clinical Research.
If interested, please fill out an application below. We're excited to speak to you!
Medpace will be hosting a Virtual Information Session regarding our opportunities for Advanced Degrees in our Cincinnati, OH and Dallas, TX offices.
WHEN: Tuesday, December 13th at 12:30pm EST
**More details regarding the format of this virtual event will be provided should you be selected to attend.
Below are the positions that will be represented at the event:
Clinical Research Associate (CRA)
Comprehensive training program that will provide you the resources and knowledge to monitor sites independently- Must be willing to travel 60-80%
- Communicates with medical staff and clinical research physicians
- Work with world class research site
Project Coordinator (PC in CRO)
Partner with Clinical Trial Manager to coordinate daily study activities- Central point of contact for internal and external team members
- Create and maintain project timeline
Associate Clinical Trial Manager
PhD in Life Sciences; Prior experience within the CRO or pharmaceutical industry not required but will be advantageous- Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
- Create and maintain project timelines
Regulatory Submissions Coordinator (RSC)
Efficiently manage and successfully execute all aspects of study start- up- Collaborate with Institutional Review Boards (IRBs)
- Prepare regulatory documents, including Informed Consent Forms
Data Coordinator
Validate an entry database design- Clean the clinical database, which includes generating and resolving data clarifications
- Perform QC audits of the clinical database
- Report metrics and data trends on projects
Medical Writer/Regulatory Writer
Write clinical study reports, protocols, and protocol amendments; regulatory related documents- Coordinate quality control reviews of documents and maintain audit trails of changes
- Project manage assignments across cross-functional
- Interact closely with the sponsor, and other Medpace subject matter experts
Regulatory Project Manager
Schedule and lead project team meetings- Coordinate project start-up activities, track and report project status, and maintain project documentation such as communication plans, submission timelines, and task orders/scopes of work
- Serve as the primary point of contact for Sponsors and regulatory authorities
Qualifications :
- Advanced Degree in life science (Masters, PhD, Post Doc experience)
- 3.0 GPA or higher
- Willing to relocate to Cincinnati or Dallas
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 more than 5,000 people across 40+ countries.
Why Medpace?:
People. Purpose. Passion. Make a Difference Tomorrow. Join Today
The work we’ve done over the past 30 years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Celebrates 30 Years
As we celebrate 3 decades of industry expertise and organic growth, we recognize the global team responsible for driving clinical development at Medpace. Click here to learn more about Medpace Celebrating 30 Years.
Cincinnati Perks
- Cincinnati Campus Overview
- Hybrid work-from-home options (dependent upon position and level)
- Competitive PTO packages, starting at 20+ days
- Flexible work hours
- Discounted tuition for UC online programs
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with local nonprofit organizations
- Competitive compensation and benefits package
- Structured career paths with opportunities for professional growth
- Partnership and discount with onsite childcare
- Discounted tuition for UC online programs
- Discounts on local sports games, local fitness gyms and attractions
- Official Sponsor of FC Cincinnati
- Modern, ecofriendly campus with an on-site fitness center, bar, and restaurants
Awards:
- Recognized by Forbes as one of America's Best Mid-size Companies in 2021 and 2022
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next:
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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