Clinical Trial Coordinator

3 weeks ago

Johannesburg, South Africa PPD Full time

**Who is PPD Clinical Research Services?**

PPD is a leading global contract research organization. Our purpose is to improve health. Our mission is to help customers deliver life-changing therapies. Our strategy is to bend the cost and time curve of drug development and optimize value for our customers. PPD is now part of Thermo Fisher Scientific. As the world leader in serving science, our Mission is to enable our customers to make the world healthier, cleaner and safer. We are excited about the opportunities this combination brings to enhance our comprehensive end-to-end offering, enabling customers to move rapidly from scientific idea to approved medicine

**The PPD FSP Solution**:
PPD's Functional Service Provider division partner with and serve as an extension of our PPD team, supporting our customers key functions. We cover customer needs on every level, allowing them to do more with less, with an uncompromising commitment to quality. We deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success.

Joining within our PPD FSP functional area, allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience.

**Clinical Trial Coordinator (client-dedicated) - South Africa**

Our clinical department defines, develops and delivers clinical programmes, ensuring the highest-quality review of data and effective interaction with study sites. As a Clinical Trial Coordinator (Client-dedicated), you will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable, working on client studies only, using their clinical systems and SOPs. Additional key responsibilities include:

- Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools
- Reviews regulatory documents for proper content
- Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified
- Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments
- Assists with the identification of potential investigators and development/distribution of initial protocol packets
- Creates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes

**Education and Experience**:

- University degree, or equivalent in education, training and experience
- Responsible for adhering to Good Clinical Practices, country specific regulations, PPD/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout
- Ability to effectively analyse project specific data/systems to ensure accuracy and efficiency
- Experience of manage multiple projects with differing priorities at one given time
- Exceptional communication, collaboration, organisational and time management skills

**Our 4i values**:

- Integrity - Innovation - Intensity - Involvement -**

**Work Environment Requirements**:

- PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive._

PPD® FSP: People Who Deliver | PPD Careers - Read about PPD employee experiences

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