Regulatory submissions (study start-up) manager

We are currently seeking a full-time Regulatory (Study Start Up) Submissions Manager to join our Clinical Operations team in Seoul, South Korea.

Responsibilities

• Experience with direct communication with MFDS, liaising between the local authorities and Sponsors to solve queries and expedite local approvals;
• Regional experience efficiently managing and successfully executing all aspects of regional start-up in APAC region;
• Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
• Present during bid defenses, general capabilities meetings, and audits.

Qualifications

• More than 5 years of experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience;
• Possess Regulatory background/ strong scientific technical knowledge;
• Regional experience will be highly advantageous;
• Excellent English oral and written communication skills.

Travel: Minimal

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

• When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence.

Collaborative Culture

Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. Leadership throughout Medpace is both accessible and approachable.

Continuous Growth & Development

• Office based environment with on-site mentors;
• Defined career paths with clear advancement opportunities;
• Industry renowned onboarding and training programs designed to accelerate professional development;
• Ongoing training and continuous learning opportunities throughout your career;
• An environment that encourages employees to influence change, contribute ideas, and grow quickly.

Other Employee Benefits

Competitive compensation programs that recognize and reward performance. Comprehensive health, wellness, retirement, and PTO benefits. Office based culture with occasional WFH that provides flexibility for eligible positions after training. Company-sponsored social events. Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.