Clinical Research Associate (Hong Kong)

Job Location(s) HK | CN-Guangzhou | MY-Petaling Jaya | AU-Melbourne
Job Number
Job Category
Clinical Research Associates
Position Type

Job Overview

Are you an exceptional Clinical Research Associate (CRA) based in Hong Kong that has independent trial site monitoring experience? 
Responsibilities include:
1) The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties.
2) Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
3) Responsible for all aspects of site management as prescribed in the project plans
4) General On-Site Monitoring Responsibilities:
5) Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
6) Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
7) Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review
8) Monitor data for missing or implausible data
9) Ensure the resources of the Sponsor and Covance are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Covance travel policy
10) Ensure audit readiness at the site level
11) Travel, including air travel, may be required and is an essential function of the job.
12) Prepare accurate and timely trip reports
13) Manage small projects under direction of a Project Manager/Director as assigned
a. Serve as lead monitor for a protocol or project, and may assist in establishing monitoring plans and trip report review as assigned
14) Review progress of projects and initiate appropriate actions to achieve target objectives
15) Organize and make presentations at Investigator Meetings
16) Participate in the development of protocols and Case Report Forms as assigned
17) Participate in writing clinical trial reports as assigned
18) Interact with internal work groups to evaluate needs, resources and timelines
19) Act as contact for clinical trial supplies and other suppliers (vendors) as assigned
20) Responsible for all aspects of registry management as prescribed in the project plans
21) Undertake feasibility work when requested
22) Conduct, report and follow-up on Quality Control (QC) visits when requested
23) Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assigned
24) Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned
25) Track and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
26) Independently perform CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management
27) Assist with training, mentoring and development of new employees, e.g. co-monitoring
28) Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned
29) Perform other duties as assigned by management


University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)


- In lieu of the above requirement, candidates with two (2) or more years of relevant clinical research experience in pharmaceutical or CRO industries may be considered
- Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements
- Basic understanding of the clinical trial process


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