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.
Medpace Perks Hybrid work-from-home options (dependent upon position and level)Competitive PTO packages Company-sponsored employee appreciation events Employee health and wellness initiatives Flexible work schedule Competitive compensation and benefits package Structured career paths with opportunities for professional growth Awards 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
廣告
Regulatory Submissions (study Start-up) Manager, Taiwan
Free
Regulatory Submissions (study Start-up) Manager, Taiwan
Taiwan, 台北, 台北市,
發表 August 31, 2024
描述
聯繫雇主
雇主信息
A therapeutically focused leader in research-based drug development, Medpace builds strong strategic partnerships with select Sponsors to advance the most efficient and cost-effective path to drug approval. As a full service, global Clinical Research Organization (CRO), Medpace sees itself as a steward of your drug, leveraging its extensive medical and regulatory expertise to deliver additional input, strategy, and efficiencies to each and every phase of the clinical trial. From custom solutions addressing the needs of small and midsize biotechnology companies to full-service offerings for global pharmaceutical companies, Medpace has the breadth, depth, and flexibility to deliver a superior result, specific to your needs, on six continents.
Specialties
Clinical Operations,
Regulatory,
IVRS,
Reference Laboratories (MRL),
Cardiovascular Core Laboratory,
Imagepace,
Clinical Pharmacology (CPU),
Medpace Bioanalytical Laboratory (MBL),
Medpace Medical Consulting (MMC),
and Medpace Medical Device,
(MMD)
