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Senior CRA 高级临床研究专员 [ 投诉职位 ]

百诺科医药科技（北京）有限公司查看地图

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基本信息

工作地点：天津市
年龄要求：20~45岁
要求学历：不限
招聘人数：3人
工作经验：3年以上
专业要求：不限

任职要求/岗位职责

Key Responsibilities:
Organize, conduct, monitor and report progress on assigned clinical trials;

Assist project teams in developing and executing project plans;

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

Provide day-to-day supervision on clinical monitoring to other CRAs;

Monitor AE &SAE during clinical trial;

Function as Lead CRA on assigned clinical trials.
Qualifications:
Bachelor degree or above in medical or relevant specialty;

Over 3 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.

企业介绍

RPS Inc., a global CRO headquartered in the US with the operations in 35 countries worldwide, provides comprehensive Phase 1-4 clinical development solutions to the pharmaceutical, biotechnology and medical device industries. By combining an experienced clinical research operations infrastructure with the industry’s largest resourcing engines, RPS is uniquely positioned to offer our Clients both integrated and full service global outsourcing solutions. These solutions are powered by highly experienced and seasoned study teams providing innovative, cost-effective and high quality services.

Our success is the result of our employees. We are able to attract the top professionals in the industry because of the unique benefits that we offer. Our specialized staff of clinical trial consultants is eager to discuss your career plans. RPS is sensitive to your daily responsibilities. Tell us EXACTLY how to contact you and we will. For your convenience, you can also submit your resume to hr@pmxintl.com.

We look forward to discussing the opportunities and benefits of employment with RPS (our corporate website: www.rpsweb.com)!