increases / decreases in consumable usage to the Clinic Supervisor as well as discrepancies in consumable report any deviation to the person in-charge of the clinic. 3.8 Documents results of all basic physical checks record sheets/Donor Questionnaires. 3.9 Inform clinic supervisor or designated deputy of all irregularities immediately. The donor will be accepted or deferred by clinic supervisor or designated deputy in case of medical advice. KPA 4 Learning and Growth 4.1 Performs Clinic Supervisor duties, roles and responsibilities,
increases / decreases in consumable usage to the Clinic Supervisor as well as discrepancies in consumable report any deviation to the person in-charge of the clinic. 3.8 Documents results of all basic physical checks record sheets/Donor Questionnaires. 3.9 Inform clinic supervisor or designated deputy of all irregularities immediately. The donor will be accepted or deferred by clinic supervisor or designated deputy in case of medical advice. KPA 4 Learning and Growth 4.1 Performs Clinic Supervisor duties, roles and responsibilities,
Thats Accelerating Research & Discovery for Clinical Trials
About We''re on a mission to revolutionize the way clinical trials are conducted. Our approach focuses on but setting the pace. We embrace the future of clinical data management by seamlessly integrating AI, are driven by a relentless passion for advancing clinical research through impeccable data management.
Integrity: informed decisions based on the highest quality clinical data
Learning and Development: Grow to help
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol areas:
Desirable
Representatives with product queries and/or technical/clinical application information
Ensure proficient
requirement
Clinical experience with knowledge of competitive products
Clinical use of Digital
Representatives with product queries and/or technical/clinical application information Ensure proficient handover is a requirement Clinical experience with knowledge of competitive products Clinical use of Digital X-Ray
Representatives with product queries and/or technical/clinical application information Ensure proficient handover is a requirement Clinical experience with knowledge of competitive products Clinical use of Digital X-Ray
role is integral to the smooth operation of our clinic, providing hands-on support to our doctors and Responsibilities: