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Assistant Clinical Research Manager

2 months ago

Bristol, Maine, United States Medpace Full time
Job Overview:

Medpace, a prominent Contract Research Organization (CRO) specializing in the biotechnology sector, is actively seeking individuals with advanced degrees, particularly PhDs or Post-Doctoral experience, for the role of Associate Clinical Trial Manager (aCTM). This full-time position is based in our Seoul, South Korea office and is integral to our Clinical Trial Management team.

The aCTM will collaborate closely with Project Coordinators and Clinical Trial Managers, assisting in various project management tasks. We are looking for candidates eager to apply their analytical and academic expertise in the realm of clinical project administration and management.

Key Responsibilities:
  • Engage in effective communication and collaboration on global study initiatives, working in tandem with project coordinators and clinical trial managers;
  • Ensure the punctual completion of recurring tasks with a high level of precision;
  • Compile and maintain detailed project-specific status reports within our clinical trial management system;
  • Interact with internal project teams, sponsors, study sites, and external vendors;
  • Oversee and ensure quality control of our internal regulatory filing systems;
  • Manage study supplies effectively;
  • Create and uphold project timelines;
  • Coordinate project meetings and produce comprehensive minutes.
Qualifications:
  • PhD in Life Sciences;
  • Proficiency in English with strong presentation capabilities;
  • Ability to thrive in a fast-paced, dynamic environment as part of an international team;
  • Previous experience in the CRO or pharmaceutical sectors is advantageous but not mandatory;
  • Exceptional computer skills (including word processing, databases, Excel, and Windows), along with strong organizational and communication abilities.
About Medpace:

Medpace is a comprehensive clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to expedite the global development of safe and effective medical therapeutics through a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across various major areas, including oncology, cardiology, metabolic diseases, endocrinology, central nervous system disorders, and anti-viral and anti-infective therapies.

Why Choose Medpace?

At Medpace, we value our people, purpose, and passion. Join us in making a difference for tomorrow. Our work over the past 30+ years has positively impacted countless patients and families facing various diseases across all key therapeutic areas. The contributions we make today will enhance the lives of individuals living with illnesses in the future.

Medpace Benefits:
  • Hybrid work-from-home options (dependent upon position and level);
  • Competitive paid time off (PTO) packages;
  • Company-sponsored employee appreciation events;
  • Health and wellness initiatives for employees;
  • Flexible work schedules;
  • Attractive compensation and benefits packages;
  • Structured career paths with opportunities for professional advancement.
Awards and Recognition:
  • Featured by Forbes as one of America's Most Successful Midsize Companies in recent years;
  • Consistently recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
Next Steps:

A member of the Medpace team will review your qualifications. If your profile aligns with our needs, you will be contacted with further details regarding the next steps.

Medpace is an Equal Opportunity/Affirmative Action Employer M/F/Disability/Vets.