Biology, Biotech and Pharmaceutical, Cardiology, Clinical Practices/Protocols, Clinical Research, Clinical Support, Clinical Trial, Clinical Trial Management, Contract Research Organization (CRO), Customer Support/Service, Disease, Drug Development, Endocrinology, Establish Priorities, Fitness, GCP (Good Clinical Practices), GMP (Good Manufacturing Practices), GxP, Leadership, Medical Equipment, Medical Products, Metabolic Disorders, Microsoft Excel, Microsoft PowerPoint, Microsoft Word, Nonprofit, Oncology, Pharmacy, Problem Solving Skills, Regulations, Research Protocols, Sports, Supply Chain
LOCATION
Cincinnati, Ohio
POSTED
30+ days ago
Job Summary:
Our Clinical Packaging & Supplies team is growing, and we are currently seeking a full-time, Clinical Packaging & Supplie Chain Project Specialist to join our team. If you want to put your pharmacy background towards an exciting career in clinical research, then this is the opportunity for you. *This position is office-based in Cincinnati, OH.
Responsibilities :
As a member of CP&S department, support and collaborate in all activities related to investigational productsupply chain;
Support CP&S department to translate clinical study protocol into investigational supply chain;
Monitor alignment of CP&S timelines with project timelines;
Attend teleconfrences with internal Medpace teams, Sponsors, and/or Vendors and communicate/present both virtually and face to face; and
Support collaboration with Clinical Trial Manager other functional areas to provide study deliverables.
Qualifications :
PharmD;
Ability to escalate;
Prioritization of daily, weekly, monthly, and project workloads;
Stong communication and problem-solving skills;
Effectively collaborate with internal and external colleagues;
Provide excellent internal and external customer support.;
Understand multiple potential solutions;
Solid working knowledge of Power Point, Excel, Word; and
Interest in a new experience in Medpace.
Understanding of GCP, GMP, GxP is preferred
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.
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.