At a Glance
- Tasks: Support clinical trials by managing documentation and coordinating study activities.
- Company: Leading global Contract Research Organization (CRO) with a dynamic environment.
- Benefits: Competitive salary, medical aid, pension, and extensive training opportunities.
- Other info: Great potential for career growth in a unique regional setting.
- Why this job: Kickstart your career in clinical research and make a real impact on healthcare.
- Qualifications: High school diploma; experience in clinical trials or healthcare preferred.
The predicted salary is between 47250 - 57750 $ per year.
About the Role
Our client, a leading global Contract Research Organization (CRO), is seeking an organized and proactive Clinical Trial Assistant (CTA) to support their Phase III clinical trial operations in the Kimberley area.
This entry-to-mid-level role is vital for ensuring the smooth running of clinical trials by providing administrative and organizational support to the clinical research team.
The CTA will assist with essential trial documentation, site management, and data coordination, playing a key part in bringing new therapies to market.
This is an excellent opportunity to gain valuable experience in clinical research within a dynamic and fast-paced CRO environment.
Key Responsibilities
- Provide comprehensive administrative support to the clinical trial team, including managing study documentation and correspondence.
- Assist with the preparation, maintenance, and filing of the Trial Master File (TMF).
- Support the process of site selection, initiation, monitoring, and close-out visits.
- Coordinate study-related activities, such as scheduling meetings, managing travel arrangements, and disseminating information.
- Assist in the collection, review, and tracking of essential study documents from clinical sites.
- Help manage study supplies and equipment, ensuring timely delivery to sites.
- Assist in tracking patient recruitment and retention efforts.
- Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, and relevant regulatory requirements.
- Liaise with investigators and site staff as directed by the Clinical Research Associate (CRA) or Clinical Project Manager (CPM).
- Contribute to the overall efficient conduct of clinical trials.
Requirements
- High school diploma or equivalent; Bachelor's degree in a life science or related field is preferred.
- Previous experience as a Clinical Trial Assistant, administrative assistant in a healthcare setting, or a related role.
- Understanding of clinical trial processes and terminology.
- Knowledge of GCP and ICH guidelines is highly desirable.
- Exceptional organizational and time management skills.
- Strong attention to detail and accuracy.
- Proficiency in Microsoft Office Suite (Word, Excel, Outlook, Power Point).
- Excellent written and verbal communication skills.
- Ability to work effectively both independently and as part of a team.
- Willingness to learn and adapt in a rapidly evolving research environment.
Benefits
Our client offers a competitive salary, comprehensive benefits package including medical aid and pension, and extensive training and development opportunities.
This role provides an excellent entry point into the clinical research industry with significant potential for career growth within the CRO.
The Kimberley location offers a unique regional setting for professional development.
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Clinical Trial Assistant in Kimberley employer: Placements24
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