Clinical Research Coordinator Part Time - Bellville South, South Africa - IQVIA

IQVIA

Verified Company

Bellville South, South Africa

2 weeks ago

Posted by:

Thabo Mthembu

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Part time

Description

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking for a Clinical Research Assistant.

This part time (24h per week) role with a start in January 2023 for 5-6 months is to support the site in
Cape Town to conduct a Neurology clinical trial.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day to day responsibilities will include:

Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
Maintain uptodate study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
Plan and coordinate logístical activity for study procedures according to the study protocol
Perform clinical setup and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
Correct custody of study drug according to site standard operating procedures
Coordinate with study monitor on study issues and effectively respond to monitorinitiated questions.
BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
Basic knowledge of clinical trials, combined with indepth knowledge of departmental, protocol and studyspecific operating procedures, consent forms, and study schedules
Basic knowledge of medical terminology
Experience in the field of respiratory disease would be a plus
Excellent interpersonal skills with the ability to establish and maintain effective working relationships with coworkers, managers and client
Good organizational skills with the ability to pay close attention to detail.