Clinical Trial Coordinator, Lisbon

PPD

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.

The role

The basic purpose of the Clinical Trial Coordinator 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.

Responsibilities include, but are not limited to: Reviews regulatory documents for proper contentPerforms PPD investigator file reviews and logging of outstanding issues in project related tracking toolsLiaises 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 departmentsAssists with the identification of potential investigators and development/distribution of initial protocol packetsCreates meeting agendas and minutesCoordinates team conference calls and distribution of meeting minutes

PPD

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.

The role

The basic purpose of the Clinical Trial Coordinator 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.

Responsibilities include, but are not limited to: Reviews regulatory documents for proper contentPerforms PPD investigator file reviews and logging of outstanding issues in project related tracking toolsLiaises 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 departmentsAssists with the identification of potential investigators and development/distribution of initial protocol packetsCreates meeting agendas and minutesCoordinates team conference calls and distribution of meeting minutes

Education and Experience: University 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 skillsExcellent organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectivelyAbility to effectively analyze project specific data/systems to ensure accuracy and efficiencyFlexibility to reprioritize workload to meet changing project timelinesResponsible 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 closeoutFluency in English and in the country's native languageExcellent computer skills, proficient in MS Word, Excel, PowerPoint and ability to obtain knowledge and master all clinical trial database systemsAbility to successfully complete PPD clinical training program (CAFT- Clinical Administration Foundation Training)Ability to mentor and train new Project Assistants as needed PPD promotes equal opportunities for all candidates. Please note that only shortlisted candidates will be contacted.

IndeedPPDEMEA1

*LI-MP1

Education and Experience: University 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 skillsExcellent organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectivelyAbility to effectively analyze project specific data/systems to ensure accuracy and efficiencyFlexibility to reprioritize workload to meet changing project timelinesResponsible 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 closeoutFluency in English and in the country's native languageExcellent computer skills, proficient in MS Word, Excel, PowerPoint and ability to obtain knowledge and master all clinical trial database systemsAbility to successfully complete PPD clinical training program (CAFT- Clinical Administration Foundation Training)Ability to mentor and train new Project Assistants as needed PPD promotes equal opportunities for all candidates. Please note that only shortlisted candidates will be contacted.

IndeedPPDEMEA1

*LI-MP1