Covance by Labcorp Job - 39435960 | CareerArc
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Company: Covance by Labcorp
Location: Shanghai, Shanghai, China
Career Level: Associate
Industries: Healthcare, Pharmaceutical, Biotech

Description

Job Overview:

Study Design Lead should be knowledgeable and experienced in study design techniques related to the creation and maintenance of the Covance Statement of Work document. Study Design Lead must possess strong knowledge of Covance processes and systems. Study Design Lead must show agility to deal with conflicting priorities and possess appropriate self management skills. 

 

1. Takes the lead to accurately interpret and translate protocol requirements in to SOW document

 

2. Leverages technical, therapeutic area, client and Covance process knowledge to provide a comprehensive and complete SOW document

 

3. Liaise with internal departments to understand Covance capabilities and assess feasibility of requests in order to meet client needs related to study design

 

4. Demonstrates strong knowledge of Covance processes and technical capabilities

 

5. Acts as a consultant to the client to advise on study design choices and works with GSM to highlight risks and budget impacts associated with study design

 

6. Displays strong interpersonal and communication skills that will build strong internal and external relationships to ensure high quality study design

 

7. Coordinates internal processes and communications related to study design (including but not limited to: internal feasibility requests, material transfer agreements and supply forecasting) and ensures the eventual follow up is integrated in to the SOW and global monitoring plan. Performs quality self-review

 

8. Ensures that all customer requirements with relation to study design are documented and acted upon

 

9. Able to act efficiently in an environment with dynamic timelines and priorities

 

10. Displays appropriate self organization and ability to manage conflicting priorities

 

11. Participate in functional meetings (eg. CLFs) and provide input, keeping processes up to date

 

12. Comply with CCLS Global Project Management strategy

 

13. Support a culture of continuous improvement, quality and productivity

Education/Qualifications:

* University degree in a scientific field

Experience: Minimum Required:
  • 7 years of previous experience in a CCLS Project Management and/or Clinical Database Design role; or other equivalent industry experience in designing clinical databases (education may be substituted for experience)


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