Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coordinator to join our Data Management team. This position involves working 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 knowledge and experience to further develop and grow your career even further, then this is the opportunity for you! Data Coordinator Training and Development Program: The Medpace Data Management Training & Development (T&D) team will partner with each new hire to help develop those that are new to the industry and add continued support for those with experience. The program encourages team training while providing opportunities for one-on-one interactions directly with a T&D member. Each new hire will be provided with the following: Online training modules that include interactive exercises T&D led workshops that ensure understanding of Data Management processes and industry acronyms Opportunities to join other new professionals in the department within the training courses Direct support from one of the team’s T&D members Responsibilities 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 Reconcile data from multiple sources Create and update study documentation on projects Participate as part of a team on various projects Qualifications Bachelor's degree in a Life Science or related field with strong attention to detail, excellent communication skills, ability to prioritize and multitask effectively, and experience with Excel and Word. Previous experience working with research and statistical data is preferred ideally in a pharmaceutical or CRO setting. 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 5,000 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 Cincinnati Campus Overview 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. Bachelor's degree in a Life Science or related field with strong attention to detail, excellent communication skills, ability to prioritize and multitask effectively, and experience with Excel and Word. Previous experience working with research and statistical data is preferred ideally in a pharmaceutical or CRO setting. TRAVEL: None 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 Reconcile data from multiple sources Create and update study documentation on projects Participate as part of a team on various projects #J-18808-Ljbffr Medpace
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