Clinical Trial Coordinator (Ref. No.: 170990)

PPD Czech Republic, s.r.o.

Place of work
Praha 47, Prague, Czechia
Contract type
Wage (gross)
2 Kč/hourCometitive

Information about the position

Job description, responsibilities and duties

PPD is a leading global contract research organization. At PPD we are passionate, deliberate, and driven by our purpose - to improve health.

PPD’s Clinical Management department is committed to industry leadership and the relentless pursuit of excellence. Working in the Clinical Management department, you will combine deep knowledge, therapeutic expertise, and robust tools to help our clients deliver life-changing therapies to market.

As a clinical trial coordinator, you will provide technical and administrative support to your assigned clinical project team. You work with a high attention to detail, reviewing documentation, coordinating project details, and maintaining data systems - all with a sense of urgency aligned with that of our customers.

Grow within the Clinical Management department into senior-level clinical trial coordinator roles or leadership roles within the department. Or, develop into Remote Site Monitor or Clinical Research Associate roles. You can also explore opportunities within other groups, such as Site and Patient Access.
The basic purpose of the Project Assistant is to provide technical support to the project team. Will coordinate non-clinical responsibilities of project administration as applicable to the client contract under the direction of the assigned Clinical Manager or Sr. Clinical Manager.

Job Qualification

Responsibilities include, but are not limited to;

Reviews regulatory documents for proper content
Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools
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
Coordinates team conference calls and distribution of meeting minutes

Education and Experience:

Bachelor's Degree or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities

Knowledge, Skills and Abilities:

Excellent communication and interpersonal skills
Excellent organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively
Ability to effectively analyze project specific data/systems to ensure accuracy and efficiency
Flexibility to reprioritize workload to meet changing project timelines

Responsible for adhering to FDA Good Clinical Practices, FDA regulations, PPD/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout

Excellent English and grammar skills
Excellent computer skills, proficient in MS Word, Excel, PowerPoint and ability to obtain knowledge and master all clinical trial database systems
Ability to successfully complete PPD clinical training program (CAFT- Clinical Administration Foundation Training)
Ability to mentor and train new Project Assistants as needed

Employee perks, benefits

At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. It's not just talk - our award winning training programs speak for themselves.

To learn how PPD can advance your career, apply now!

What To Expect Next

We look forward to receiving your application. A member of our talent acquisition team will review your qualifications and if interested, you will be contacted for an interview.

Requirements for the employee

Candidates with education suit the position

University education (Bachelor's degree)

Language skills

English - Advanced (C1) and Czech - Advanced (C1)


Brief description of the company

PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our customers include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 46 countries and approximately 23,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help customers bend the cost and time curve of drug development and optimize value in delivering life-changing therapies to improve health.

Number of employees

1000 and more employees

Company address

PPD Czech Republic, s.r.o.
Budejovicka alej, Antala Staska 2027/79
140 00 Praha 4


Contact person: Maria Mazneva
E-mail: send CV
ID: 3929665  Datum zveřejnění: 26.6.2020  Spodní hranice mzdy (brutto): 2 Kč/hour