CRA – Clinical Research Assistant

We are currently recruiting Clinical Research Assistant to join the Clinical Operations. We are looking for people interested in full-time options!
 
About the Job:
Act as contact for project team and study sites
Perform CRF review, query generation and resolution against established data review guidelines, under direct supervision, as assigned by management
Assist with the management of study equipment and supplies and organize shipments
Create, update, track, and maintain study specific trial management files, tools and systems
Assist in submissions and notifications to Ethics Committees and Regulatory Authorities
General On-Site Monitoring Responsibilities – Initiate, monitor and close out clinical investigator sites under direct supervision from Clinical manager, including establishing monitoring reports.
Assist with on-site tasks as required and according to training goals (e.g. review of Case Report Forms and Study File docs, device accountability…)
Perform other duties as assigned by management
Collaborate with study team members for project execution support as appropriate
We offer opportunities to work on diverse, challenging projects while building a flexible and rewarding career.
Requirements:
University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
Previous monitoring experience
Ability to work to tight deadlines
Good organizational and time management skills
Good communication skills oral and written
Exhibit General computer literacy
Advantage for good online articles/Information searching and reading skills
Good in local office language and English, both written and verbal
Ability to establish and maintain effective working relationships with coworkers, managers and clients