[台北] 育世博生技 诚征 临床专案经理

楼主: joeowl (I was born to love you)   2020-02-12 12:02:24
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Acepodia just receives its first IND clearance for clinical study in US.
More to come in 2020 and 2021.
We are looking for talents in clinical operation for this exciting adventure.
Share with your resume with us if interested.
【公司名称】
Acepodia Biotech Inc. 育世博生物科技股份有限公司
【工作职缺】
Clinical Program Associate Manager 临床专案经理
【工作内容】
‧ Provides support to Project Team and Clinical Operations Team.
‧ Maintains strong working knowledge of protocols, manuals, and site-facing
documents for assigned clinical studies.
‧ Set and enforce project timelines with the assigned study team.
‧ Assists project team in development of site-facing documents, operation
manuals, training material, and tools.
‧ Responsible for assuring needs of clinical sites are met by facilitating
CRO.
‧ Support site start-up activities and ensure that sites have sufficient
project specific supplies.
‧ Participates in site audits, as requested.
‧ Conduct project co-monitoring visits and team training.
‧ Participates and provides support for relevant study meetings, e.g. safety
meetings, CRO meetings, medical advisor meetings, and other internal and
external meetings.
‧ Proactively identifies, manages, escalates (as needed) and resolves site
issues effectively and independently.
‧ Provides support to Project Team and assume additional roles on the team
as necessary.
‧ Other duties as assigned by Clinical Operations Manager/Project Manager
and per project-specific requirements (i.e. project presentation, project
timeline and budget, project bidding, service procurement, etc.).
‧ May be assigned to the project team in the joint project with other
departments (e.g. business development, operations)
‧ Job title may be adjusted based applicant experience and skillset
【征求条件】
#Required Education and Experience
‧ College/University graduate or above (degree in healthcare or life science
degree is a plus).
‧ 2 years of monitoring experience gained from a CRO and/or other related
clinical research environment.
‧ Experience in clinical patient management, preparing of clinical
site-facing documents, and ensuring compliance with protocol and GCP.
#Required Knowledge, Skills and Competencies
‧ Strong English language written and verbal communication skills.
‧ Strong interpersonal skills and team player.
‧ Highly organized with exceptional attention to detail.
‧ Computer literacy with high proficiency in MS word and powerpoint.
‧ Interested in working in a start-up environment that is dynamic and
fast-paced.
‧ Honest work ethic and shared goal in promoting development of treatments
for patients.
#Physical Requirements
‧ Minor lifting, < 30 lbs
‧ Must work from Corporate-office location
‧ Regular sitting and keyboard use
‧ May require occasional domestic and/ or international business travel.
‧ Ability to travel up to 10%.
‧ May require occasional international teleconferences
【工作地点】
新北市汐止区新台五路一段99号17楼之7
【工作时间】
9:00-18:00 (午休一小时)
【月休】
按照人事行政局,见红就放
【公司福利】
员工团保(医疗/寿险/意外险)、公司停车位提供、租屋补助、员工配股、
特休优于劳基法(第一年12天)、14天有薪病假
【薪资范围】
依工作经验及能力叙薪 (月薪 > 45000)
【需求人数】
1人
【联络人/连络方式】
赖经理
02-26976100 #13
[email protected]
【其他备注】
Official website:
https://www.acepodia.com/
104:
https://www.104.com.tw/job/6ur73?jobsource=company_job

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