Clinical Cosmetic Support Researcher

Job description

We are looking for a meticulous and skilled support Researcher to join our clinical research team. The ideal candidate will be responsible for ensuring that the administrative aspects of our clinical studies are executed with precision, adhering to the highest quality standards. You will play a critical role in setting up and conducting trials, ensuring regulatory compliance, and maintaining accurate documentation.

The position will be based in Panorama, Northern Suburbs

Key responsibilities:

• Assist in setting up clinical trials, ensuring laboratory equipment is in working order and compliant with company procedures.
• Participate in the admission and inclusion of volunteers, ensuring adherence to study protocols.
• Capture and manage raw data accurately, ensuring quality control in line with company and regulatory guidelines.
• Conduct quality checks on study documentation and ensure accurate record-keeping.
• Maintain study facilities, ensuring environmental conditions (e.g., temperature, humidity) meet required standards.
• Record and manage investigational products according to protocol.
• Ensure compliance with Good Clinical Practices (GCP) and ISO 9001 standards.
• Promptly report any deviations, malfunctions, or quality concerns to the appropriate personnel.
• Perform routine administrative tasks related to volunteer selection and management (e.g., data entry, document classification, mailing).
• Assist in the control, preparation, and application of test products during trials.

Requirements

Key requirements

• Experience: Previous experience in a clinical, laboratory, or research environment (preferably in cosmetics or dermatological studies) advantageous.
• Administration Skills: Provide admin support relating to necessary documentation and data collation for the trials.
• Technical skills: Knowledge of laboratory procedures, equipment handling, and data capture methods.
• Regulatory knowledge: Familiarity with Good Clinical Practices (GCP), ISO 9001, and standard clinical trial procedures advantageous.
• Attention to detail: Strong data accuracy and quality control skills.
• Communication skills: Ability to report findings clearly and work collaboratively with a multidisciplinary team.
• Problem-solving: Ability to identify and escalate technical issues or study deviations efficiently.

Posted on 14 Mar 15:39, Closing date 13 May