Adverse Events, Biology, Biostatistics, Biotech and Pharmaceutical, Cardiology, Clinical Data, Clinical Research, Clinical Support, Clinical Trial, Contract Research Organization (CRO), Data Management, Disease, Drug Development, Endocrinology, Fitness, Industry Standards, Leadership, Medical Coding, Medical Dictionary for Regulatory Activities (MedDRA), Medical Equipment, Medical Terminology, Medications, Metabolic Disorders, Nonprofit, Nursing, Oncology, Pharmacy, Regulations, Reporting Skills, Sports
LOCATION
Cincinnati, Ohio
POSTED
18 days ago
Job Summary:
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coder to join our Clinical Coding & Support team in Cincinnati, OH. 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 coding, pharmacy, or nursing expertise and can develop and grow your career even further, then this is the opportunity for you!
Responsibilities :
Perform accurate coding of medical terms and medications utilizing industry-wide standards as well as company standards;
Coordinate the assignment of appropriate dictionaries for meeting study requirements
Develop and maintain coding guidelines;
Issue queries on adverse events, medications, and medical history terms to ensure high quality coding;
Work collaboratively with the Medical, Data Management, Safety and Biostatistics teams to meet needs of the study; and
Produce coding reports for team review and utilization
*Stable schedule with no weekends, no work on Medpace holidays, and flexible work schedule*
Qualifications :
BSN and RN with applicable experience is required, or more advanced clinical degree (including PharmD) is accepted;
Strong critical thinking, organizational, and multi-tasking skills required;
Experience with using MedDRA and WHO Drug dictionaries preferred; and
Experience working with clinical trials or within the pharmaceutical environment is preferred.
TRAVEL: None
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.