Skip to main contentA logo with &quat;the muse&quat; in dark blue text.
Quintiles

Your career start in clinical research - Clinical Trial Assistant (CTA) position (based in Athens, Greece)

Quintiles applies the breadth and depth of our service offerings along with extensive therapeutic, scientific and analytics expertise to help our customers navigate an increasingly complex healthcare environment as they seek to improve efficiency and effectiveness inthe delivery of better healthcare outcomes. To learn more about Quintiles, please visit www.quintiles.com

PURPOSE

Provide administrative support to clinical projects under direction of line manager, Clinical Research Specialist and/or other designated clinical team members. Assists with general administrative functions as required.

RESPONSIBILITIES

Assist Clinical Research Specialist (CRS)/In-house Clinical Research Specialist (iCRS), Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.

Want more jobs like this?

Get jobs delivered to your inbox every week.

By signing up, you agree to our Terms of Service & Privacy Policy.

Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness.

Assist CRS/iCRS, CRAs/iCRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.

Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.

Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.

May perform assigned administrative tasks to support team members with clinical trial execution.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

Awareness of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Knowledge of applicable protocol requirements as provided in company training

Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint

Good written and verbal communication skills including good command of English language

Effective time management and organizational skills

Ability to establish and maintain effective working relationships with coworkers, managers and clients

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

High or Secondary School diploma/certificate or country’s educational equivalent and 3 years administrative support experience; or equivalent combination of education, training and experience

Job ID: 97269ce52e362082c93e2a90e4bda2db
Employment Type: Other

This job is no longer available.

Search all jobs