北京招聘

Responsibilities

• Efficiently manage and successfully execute all aspects of global start-up;
• Perform quality checks on submission documents and site essential documents;
• Prepare and approve informed consent forms;
• Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
• Present during bid defenses, general capabilities meetings, and audits.

Qualifications

• More than 5 years of experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience;
• Regional experience will be highly advantageous
• Strong oral and written communication skills.

Kindly submit an English version of your resume. 

Please note that actual job title will be in line with candidate experience.

北京MEDOACE医药科技有限公司是一家美资独资在全球排名前十的CRO 公司，主要为欧美及亚太地区的新药上市提供临床监察，注册，数据统计及实验室服务。公司总部设立在美国俄亥俄州的辛辛那提，全球有超过4500名员工分布在28个国家。