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1、CRA and Senior CRA based in Beijing 

1)  CRA:                                                                                                                                                                                                                                                                                                                                   Requirements:
At least 1 year working experience as CRA/monitor, or have managed at least 2 clinical trials as monitor;
Major in clinical medicine, bachelor's degree or above;
Good English skill;
Good communication skill and team spirit; good computer skill.

Responsibilities:
As main connection with investigators, to monitor clinical study from site selection to on site monitoring, to make sure clinical trial is conducted in compliance with ICHGCP, with the requirements of Regulation and sponsor.

Excellent candidates may have chances to be recommended to multinational pharmaceutical companies to obtain enough training and as CRA do one year global trial at first.

2）Senior CRA:
                Requirements:                                                                                                                                                        At least 2 years working experience as CRA/monitor, or have managed at least 4 clinical trials as monitor;
Major in clinical medicine, bachelor's degree or above;
Good English skill with CET-6 certificate or TOFEL/GRE achievement;
With good communication skill and team management ability, good computer skill.

Responsibilities:                                                                                                                                                    As main connection between sponsor and site PIs, with suppliers such as central lab or courier, to organize and monitor clinical study from site selection to on site monitoring, to make sure clinical trial is conducted in compliance with ICHGCP, in compliance with the requirements of Regulation and sponsor;
To develop and review study documents, including protocol, ICF, IB, study instruction manual, study specific procedures...
To manage the project study team and supervise CRAs, to make sure clinical trial progress smoothly and is conducted in different sites with good quality and same standard;
To keep good relationship with sponsor, to report study progress periodically;
To participate in project proposal development to support business development work;

Excellent candidates may have chances to be recommended to multinational pharmaceutical companies to obtain enough training and as CRA or study leader do one year global trial at first.