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2017-42695

2017-42695

Title 
Clinical Team Manager (CLM) - BJ (CN)
Job Locations 
-
China
Posted Date 
9/3/2017

More information about this job

Overview

As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.

 

At PRA Health Sciences, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

 

At PRA, borders do not create boundaries.  PRA’s success is dependent upon our ability to attract and retain a talented team of diverse professionals.  Our growing workforce is comprised of over 10,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages – yet operate in unison as one worldwide PRA community. 

Responsibilities

The Clinical Team Manager (CTM) is accountable for achieving successful delivery of clinical activities at the project level by meeting internal and external contractually agreed client and regulatory requirements according to time, quality/scope and budget constraints. The CTM leads and directs cross functional teams (Clinical Operations, Regulatory Affairs) and understands/manages client expectations. The CTM proactively identifies, resolves/mitigates and escalates risks and/or issues. Depending on the business unit the descripted ccountabilities may or may not apply.

  • Applies knowledge of PRA’s policies and procedures
  • Manages international clinical teams and multiple trial deliverables
  • Demonstrates excellent written and oral communication with internal/external teams and with the customer
  • Reads, writes and speak fluent English; and is fluent in host country language
  • Demonstrates excellent knowledge of ICH/GCP
  • Utilizes clinical knowledge to develop and implement task and trial specific training
  • Accurately projects work and resourcing requirements
  • Interactions with multi-functional teams and with the sponsor
  • Contributes to the preparation and presentation of bid defenses
  • Understands associated functions as they relates to Clinical/Trial Management
  • Demonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, and Electronic Data Capture platforms

Qualifications

  • 3+ years of clinical research experience required
  • Read, write and speak fluent English; fluent in host country language required.



  • Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required.



  • 2+ years monitoring experience preferred





PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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