Clinical Cosmetic Support Researcher

Job description

• 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

• Experience: Previous experience in a clinical, laboratory, or research environment (preferably in cosmetics or dermatological studies).
• 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.
• 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.