Clinical Research Project Coordinator

Medpace; São Paulo; On-site; BRL 80,000 - 100,000; Full time

Benefits offered by this job

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

Job summary

Medpace is looking for a full-time Clinical Research Project Coordinator in São Paulo. This role involves engaging in clinical trial management and collaborating closely with project teams to ensure timely task completion and high accuracy. The ideal candidate holds a Bachelor's degree in health sciences, has prior experience in a similar role, and possesses excellent communication and organizational skills. Medpace offers a flexible work environment and a competitive compensation package with benefits.

Qualifications

• Bachelor's degree in a health sciences field required.
• Prior experience as a Study Coordinator or within the pharmaceutical industry preferred.
• Fluency in English is mandatory.

Responsibilities

• Engage in clinical trial management on a day to day level.
• Work closely with the project CTM for timely delivery of recurrent tasks.
• Compile and maintain project-specific status reports.
• Interact with Sponsor, study sites, and internal associates.
• Create and maintain project timelines.
• Coordinate project meetings and produce quality minutes.

Skills

Excellent computer skills

Organizational skills

Communication skills

Fluency in English

Education

Bachelor's degree in a health sciences field

Tools

Word-processing software

Databases

Excel

Windows

Job description

Join Medpace in Sao Paulo! Our clinical trial activities in South America are increasing rapidly! We are currently seeking a full-time, office-based Clinical Research Project Coordinator to join our Clinical Trial Management team. 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.
• Interact with the Sponsor, study sites, and internal associates.
• Create and maintain project timelines.
• Coordinate project meetings and produce quality minutes.

Qualifications

• We kindly ask that you submit your CV in English***.
• Bachelor's degree in a health sciences field required.
• Prior experience as a Study Coordinator or within the pharmaceutical industry preferred.
• Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.
• Fluency in English.

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.