Clinical Project Coordinator - Entry at Medpace, Inc.

Taipei, , Taiwan -

Full Time

Start Date

Immediate

Expiry Date

08 Apr, 26

Salary

0.0

Posted On

08 Jan, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Management, Project Coordination, Status Reporting, CTMS Updates, eTMF QC, Study Plans Drafting, Site Feasibility Management, Communication Skills, Organizational Skills, Computer Skills

Industry

Pharmaceutical Manufacturing

Description

We are currently seeking a full-time, office-based Clinical Research Project Coordinator Entry to join our Clinical Trial Management team in Taiwan (Taipei). 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 expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Engage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports; Update CTMS with study milestones, enrolment projections etc. Update eTMF and perform ongoing eTMF QC; Support clinical trial manager to draft study plans and study specific guidance documents; Manager site feasibility, site activation preparation and study supply managements; Communicate with regional cross functional team, vendors and sponsor effectively; Qualifications Bachelor's degree in a health sciences field; Maintain thorough knowledge of project and ability to coordinate/present at internal/external meetings and conference calls; Excellent computer (word-processing, databases, Excel, Windows) and organizational skills. 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. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives 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 What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Responsibilities

The Clinical Project Coordinator will engage in daily clinical trial management and work closely with the project CTM to ensure timely delivery of tasks. Responsibilities also include compiling project-specific status reports and supporting the clinical trial manager in drafting study plans.