东莞招聘

Responsibilites:

-Planning of project activities and local study timelines based on marketing objective

-Tracking study progress (e.g. local investigator meeting, initiation meeting, review meeting), ensuring the quality and assessing overall status of the project.

-Manage the project budget

-Coordinate and arrange all project trial master files for archiving at the end of the study.

-To ensure the company or sponsor SOPs, GCP and study protocols are adhered to.

-Track study progress and ensure project are conducted according to the plan.

-Identify key issues and evaluate strategies to ensure the trial's timeline and budget

-Communicate with the team on new study information, study timelines and goals, study requirements.

- Communicate with sponsor for overall status of the project and issues

-Provide ongoing training to staff with regards to ICH-GCP, study protocol and requirements.

Skills/Experience

Bachelor's Degree or above from accredited institution.

Degree in Life Sciences preferred.

Fluent in the English language and local languages as applicable

Minimum of 3 years clinical research experience;

Clinical research based managerial/supervisory experience; Prior CRO experience is preferable

Ability to travel as needed;

Ability to work independently

CRO行业2年PM实际经验，英语听说读写熟练

作为亚洲领先的招聘整体解决方案提供商，科锐国际人力资源有限公司成立于1996年，目前在大中华地区拥有12个直属分公司及34个重点城市分支机构，超过900名专业招聘人员。科锐国际致力于在17个细分行业与领域中为客户提供最优质的服务，以满足客户在所有层次的招聘需求。科锐国际的客户80%来自世界知名集团，20%来自国内上市公司、快速成长性企业及非赢利组织。在过去的一年中，科锐国际成功为企业推荐的长期雇员及派遣雇员总数超过万人，中高级专业职位及管理职位超过4500个。