Job Description
Medpace will be hosting an In-Person Hiring Event targeting Bachelor's students in life sciences.
WHEN: August 28th at 5:30 PM **More details regarding the location of the event will be provided should you be selected to attend.
Responsibilities Below are the positions we will be recruiting for at this event:
Clinical Data Coordinator: - Validate entry database designs
- Report metrics and data trends on projects
- Identify data conflicts and issues on projects
- Work with personnel from global research sites to resolve data conflicts
Clinical Research Associate - Comprehensive training program that provides resources and knowledge to monitor sites independently
- Travel to non-local, national study sites 60-80% of the time
- Communicate with medical staff and clinical research physicians on site
Project Coordinator - 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
Regulatory Submissions Coordinator - Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial;
- Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);
- Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards
Clinical Trial Proposal Writer
- Review and analyze Request for Proposal (RFP) and Request for Information (RFI) documents to gain understanding of client requirements and assist in identifying missing informationReview
- Draft standard documents in accordance with agreed strategy and Sponsor requirements within often expedited timelines
- Contribute to assigned process improvement initiatives and support implementation
- Define action plans and timelines; manage and determine modifications needed to ensure proposal alignment with client requirements and business strategies
Qualifications - 3.4-3.5 GPA or higher
- Bachelor's in Life Sciences or related fields
- Willing to work office-based in Cincinnati, OH
Medpace Overview 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 6,000 people across 40+ countries.
Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us 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.
Cincinnati Perks - Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with local nonprofit organizations
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Structured career paths with opportunities for professional growth
- Discounted tuition for UC online programs
Awards - Named a Top Workplace in 2024 by The Cincinnati Enquirer
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- 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.
Job Tags
Permanent employment, Contract work, Work at office, Local area, Immediate start, Flexible hours,