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Sr CRA I

Covance 5/16/2018 1:17:28 PM
JOB ID: 19778 Category: Clinical Operations
Beijing, China

   

 

Job Overview

* 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
* Responsible for all aspects of site management as prescribed in the project plans
* General On-Site Monitoring Responsibilities:
* Ensure the study staff who will conduct the protocol have received the proper materials and instmctions to safely enter patients into the study
* Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
* Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. Monitor data for missing or implausible data
* 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
* Prepare accurate and timely trip reports
* Manage small projects under direction of a Project Manager/Director as assigned
* Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans as assigned
* Review progress of projects and initiate appropriate actions to achieve target objectives
* Organize and make presentations at Investigator Meetings
* Report, write narratives and follow-up on serious adverse Experience s
* Participate in the development of protocols and Case Report Forms as assigned
* Participate in writing clinical trial reports as assigned
* Interact with internal work groups to evaluate needs, resources and timelines
* Act as contact for clinical trial supplies and other suppliers (vendors) as assigned
* Responsible for all aspects ofregistry management as prescribed in the project plans
* Undertake feasibility work when requested
* 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
* Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned
* Complete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
* Independently perform CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management
* Assist with training, mentoring and development of new employees, e.g. co-monitoring
* Co-ordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned
* Perform other duties as assigned by management

Education/Qualifications

Required:

* University/college degree (life science preferred), or certification in a related allied health
* Profession from an appropriately accredited institution, nursing certification, medical or laboratory technology
* In lieu of the above requirement, candidates with three (3) or more years of relevant clinical research Experience in pharmaceutical or CRO industries will be considered
* Thorough knowledge of CH Guidelines and GCP including a basic understanding of regulatory requirements in other countries
* Thorough understanding of the drug development process
* Fluent in local office language and in English, both written and verbal

Preferred:

* Thorough knowledge of Covance SOPs regarding site monitoring

Experience

Required:

* Minimum of three (3) years of clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits)
* Inlieu of the above requirements, candidates with > three (3) years supervisory Experience in a health care setting and two (2) years clinical research Experience in the pharmaceutical or CRO industries (including monitoring) may be considered
* Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
* Excellent site monitoring skills
* Excellent study site management skills
* Excellent registry administration skills
* Ability to work with minimal supervision
* Good planning and organization skills
* Good computer skills with good working knowledge of a range of computer packages
* Excellent verbal and written communication skills
* Ability to resolve project-related problems and prioritizes workload for self
* Ability to work within a project team
* Works efficiently and effectively in a matrix environment

Preferred:

* One (1) or more year's additional Experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred
* Local project coordination and/or project management


Position Type: Full-Time

Location: Beijing, CHN - China



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Below is a general Overview of Our Recruiting Process

If you’d like to work for us, please submit your resume/CV online. If your ability to use or access our electronic application is limited due to a disability, please visit www.gettinghired.com or call 1-800-978-4473 for help.

We consider applications from everyone who is interested in a position with us and who meets the required criteria and qualifications.

If your application is selected, someone from our recruiting team will contact you to arrange an initial screen. We may carry this out over the phone or at a face-to-face meeting. You must complete the screen to be considered for the position.

Based on the results of the initial screen, we may invite you to an interview. One of our recruiting team members will contact you to arrange this. The process may involve several interviews, initially over the phone, and then face-to-face with different members of the hiring team.

Our interviews follow a behavioral-based format. This means we’ll ask you to give us information that’s specific to your professional and educational experiences.

Hiring team members will share and discuss their input and then make their decision.

If you’re the person who best meets the requirements of the position, a member of the hiring team will get in touch to make you an offer of employment. Covance is an eVerify employer (United States only).