We are looking for a Clinical Trial Coord.
As a Clinical Trial Coordinator, you will provide administrative and technical support to the Project Team.
You will support audit readiness by ensuring files are reviewed on schedule detailed in the organization's WPD and department guidance document.
As a Clinical Trial Coordinator, you will provide administrative and technical support to the Project Team.
You will support audit readiness by ensuring files are reviewed on schedule detailed in the organization's WPD and department guidance document.
Requirements:
Education and Experience:
– High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification. – Bachelor's degree preferred. – Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills, Abilities:
– Ability to work in a team or independently as required – Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively – Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency – Strong customer focus – Flexibility to reprioritize workload to meet changing project timelines – Proven ability to attain and maintain agood working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout – Good English language and grammar skills and proficient local language skills as needed – Advanced digital literacy, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems – Ability to successfully complete PPD clinical training program – Self-motivated, positive attitude and good interpersonal skills.
Education and Experience:
– High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification. – Bachelor's degree preferred. – Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills, Abilities:
– Ability to work in a team or independently as required – Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively – Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency – Strong customer focus – Flexibility to reprioritize workload to meet changing project timelines – Proven ability to attain and maintain agood working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout – Good English language and grammar skills and proficient local language skills as needed – Advanced digital literacy, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems – Ability to successfully complete PPD clinical training program – Self-motivated, positive attitude and good interpersonal skills.
This position is open to all candidates.
