Clinical Trial Associate
Precision Robotics (Hong Kong) Limited
- Company Industries:Trading and Distribution
Job Information
- Post Date:2022-05-27
- Career Level:Entry Level
- Location:Shatin Area
- Yr(s) of Exp:2 years
- Qualification:Degree
- Employment Type:Full Time, Permanent
- Job Function:Medical Services Specialist
- Benefits:Dental insurance, Medical insurance, Performance bonus, Five-day work week
Job Description
Clinical Trial Associate (CTA) – a clinical trial associate is responsible for supporting the clinical and preclinical studies of our surgical robotic technologies. The CTA shall work closely with the company’s R&D team, and work with research nurses, nursing/surgical staffs, researchers, clinicians, and surgeons of our collaborating hospitals/universities. The CTA shall be responsible for the arrangement/organisation of clinical/pre-clinical studies, collecting data, updating/maintaining the documentations of the studies, supporting regulatory and ethical application processes, disseminating necessary information, facilitating the process of the studies and other laboratory experiments, and ensuring the compliance of quality assurance and safety guidelines.
Tasks/responsibilities
- Support the set up and arrange of clinical/pre-clinical trials;
- Collect and document clinical trial information in accordance with the applicable Good Clinical Practice (GCP) guidelines for clinical studies;
- Identify needs, bottlenecks and deviation found during the studies;
- Participate in research and development projects on request, or take on other tasks which contribute to the optimisation of the processes within the company;
- Support the preparation of ethical and regulatory approval processes;
- Design and perform preliminary tests prior to clinical/pre-clinical studies;
- Record the experiments/tests/studies/trial results and generate the associated reports for internal use and for regulatory approval processes;
- Perform other related duties as assigned by the supervisor
Your background and profile
- The candidate should possess a bachelor’s degree or above in biomedical engineering, medicine, medical/life sciences, clinical research management, quality management or related disciplines, with at least 3 year post-qualification experience in clinical studies, trial management or operations.
- Experience in medical devices development or associated research/clinical studies;
- Good communication skills of written and spoken English and Chinese;
- Good knowledge of Good Clinical Practice (GCP) and regulations of clinical trials are necessary.
- Excellent organisation skills
- Excellent Computer skills
Company Info
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