Undergraduate Project Assistant

Medpace; São Paulo; Presencial; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A clinical research organization in São Paulo seeks a full-time Assistant for their Safety Department. This role includes distributing safety reports, creating project trackers, and performing quality control reviews. Candidates should have a high school diploma, ideally pursuing a life science degree, with strong organizational skills and fluent English. Join a team dedicated to developing effective medical therapeutics.

Serviços

On-site fitness center

Company-sponsored social events

Discounts for local businesses

Qualificações

• High school diploma required, ideally studying for a bachelor's degree in life science.
• Ideally some administrative experience in a business setting.
• Experience of being involved with any audits will be advantageous.
• Good organisational skills and attention to detail.
• Excellent written and oral communication skills.
• Computer literacy (Microsoft Office Package).
• Fluency in English.

Responsabilidades

• Responsible for the distribution of safety reports to regulatory authorities.
• Create and maintain project-related trackers and status reports.
• Distribute and track safety-related notifications.
• Conduct quality control reviews of departmental documents.
• Perform other tasks as needed.

Conhecimentos

Organizational skills

Attention to detail

Excellent written communication

Fluency in English

Formação académica

High school diploma, ideally studying for a bachelor's degree in life science

Ferramentas

Microsoft Office Package

Descrição da oferta de emprego

Join Medpace in Sao Paulo! Our South American activities are rapidly expanding and we are currently seeking a full-time, office-based Assistant to join our Safety Department. Full training in the role will be provided. The successful candidate will work as part of a team to accomplish tasks and projects, which are instrumental to the company’s success. If you are looking for an exciting opportunity where you can use your previous expertise to develop and grow your career even further, then this is the role for you.

Responsibilities

• Responsible for the distribution of safety reports to regulatory authorities;
• Create and maintain project-related trackers and status reports;
• Distribute and track safety-related notifications;
• Conduct quality control reviews of departmental documents;
• Perform other tasks as needed.

Qualifications

• High school diploma required, ideally studying for a bachelor's degree in life science;
• Ideally some administrative experience in a business setting;
• Experience of being involved with any audits will be advantageous;
• Good organisational skills and attention to detail;
• Excellent written and oral communication skills;
• Computer literacy (Microsoft Office Package);
• Fluency in English

We kindly ask that you submit applications in English.

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?

When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.

Organic Growth: Medpace is continuing to grow in all areas globally and has built an expansive research campus at its headquarters in Cincinnati, OH. In 2020, Medpace opened a new seven story building that is approximately 250,000 SQFT. In total, the headquarter's campus includes five buildings and approximately 600,000 SQFT. The company also has expanding office locations in Dallas, TX and Denver, CO.

Perks (vary by location and position):

• On-site fitness center(s)
• Campus walking paths
• Company-sponsored social and wellness events
• Official Sponsor of FC Cincinnati
• On-site Market Place
• Free and covered parking
• Discounts for local businesses
• On campus restaurantsand banks coming soon

Awards:

• Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
• Recognized by Forbes as one of America's Best Mid-size Companies in 2021
• Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
• Ranked in the top 10 on the 2021 LinkedIn Top Companies list in Cincinnati

What to Expect Next:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.

EO/AA Employer M/F/Disability/Vets

• High school diploma required, ideally studying for a bachelor's degree in life science;
• Ideally some administrative experience in a business setting;
• Experience of being involved with any audits will be advantageous;
• Good organisational skills and attention to detail;
• Excellent written and oral communication skills;
• Computer literacy (Microsoft Office Package);
• Fluency in English

We kindly ask that you submit applications in English.

• Responsible for the distribution of safety reports to regulatory authorities;
• Create and maintain project-related trackers and status reports;
• Distribute and track safety-related notifications;
• Conduct quality control reviews of departmental documents;
• Perform other tasks as needed.