求助：翻译几条英文

Key Responsibilities:

Organize and monitor clinical trials from study kickoff to closeout;

Assist with the development of study specific monitoring plan and other study related plans & forms;

Completes in-house monitoring activities as appropriate;

Organize investigator meetings, give presentations and provide training at investigators meetings as appropriate;

Monitor AE &SAE during clinical trial.
Qualifications:

Bachelor degree or above in medical or relevant specialty;

Over 1 years CRA experience;

Good verbal and written communication skills;

Proven ability to communicate in English;

Strong sense of responsibility and dedication;

Excellent interpersonal skills;

Teamwork spirit.

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