CTA

Key responsibilities:

According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.

Performs department, Internal, Country and Investigator file reviews as assigned.

Ensures allocated tasks are performed on time, within budget and to a high-quality standard. Proactively communicates any risks to project leads and line manager as appropriate.

Supports the maintenance of study specific documentation and global support with specific systems, tools and trackers.

Provides system support (i.e. GoBalto & eTMF).

Supports RBM activities.

Performs administrative tasks including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members.

Supports scheduling of client and/or internal meetings with completion of related meeting minutes.

Reviews and tracks local regulatory documents.

Transmits documents to client and centralized IRB/IEC.

Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation.

Maintains vendor trackers.

Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites.

Assists with study-specific translation materials and translation QC upon request.

May attend Kick off meeting and take notes when required.

Keys to Success:

Education

Bachelor's degree preferred.

Previous experience that provides the knowledge, skills, and abilities to perform the job

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

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

Ability to work in a team or independently as required

Ability to handle multiple tasks efficiently

Ability to analyze project-specific data/systems to ensure accuracy and efficiency

With flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines

Ability to attain and maintain a good understanding of applicable Country Regulations, ICH and organization/Client SOPs and WPDs and closeout

Strong English language and grammar skills and proficient local language skills as needed

Strong IT skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems

Ability to complete CRG clinical training program

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