LinkedInMike Chiu
Mike Chiu

Mike Chiu

Clinical Research Professional

Location
Ascot, Berkshire, United Kingdom
Industry
Pharmaceuticals
Current
  1. Covance,
  2. Chiron Research Services Ltd.
Previous
  1. Glenmark Pharmaceuticals,
  2. Allergan,
  3. Chiltern International
Education
  1. Cranfield University
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500+connections
Covance

Covance

Clinical Research Associate

– Present

View full profile

Background

Experience

Clinical Research Associate

Covance
– Present (3 months)

Director

Chiron Research Services Ltd.
– Present (2 years 4 months)Letchworth Garden City

Freelance Clinical Research Associate

Glenmark Pharmaceuticals
(1 year 1 month)Watford, United Kingdom

Freelance Clinical Research Associate

Allergan
(11 months)Marlow

Clinical Research Professional

Chiltern International
(1 year)Slough

Clinical Trials Monitor

Roche Pharmaceuticals
(1 year)Welwyn

Responsible for performing study site management activities related to start up and close out activities, regulatory compliance, patient enrollment, protocol adherence, CRF compliance and data quality for clinical trials so that they meet specified scientific, medical, regulatory and commercial needs as well as developing and maintaining investigator relationships.

Clinical Research Associate

Novella Clinical, Inc.
(5 months)Stevenage, United Kingdom

Responsible for monitoring Novella clinical trials to ensure that investigators are conducting the research within requirements of the clinical protocol, that research is conducted in accordance with applicable federal regulations and guidelines, that data quality on initial review meets acceptable clinical standards, and the rights and safety of human subjects involved in a clinical study are protected.

Senior Project Coordinator

Novella Clinical
(2 years)

Responsible for supporting project managers' thorough planning, implementation and effective execution of contracted clinical trials. Responsible for supporting project teams both administratively and technically as appropriate. Provides project administrative support including agenda and minute documentation, monthly reports, shipping, filing, tracking, and status summarisation as appropriate. Participate and assist in the planning and creation of client and investigator meetings and related materials. Provide other administrative support, as assigned.

Clinical Packaging Supervisor

Merck
(1 year)

Generation of batch documentation for the packaging of clinical supplies to global sites in accordance with safety and GMP requirements. The role included the supervision of packaging operators, ensuring technicians meet their goals, and training of new technician personnel in job activities. Reporting to an Operations Section Leader.

Languages

  1. Chinese

Skills

  • Clinical Trials
  • CRO
  • CTMS
  • GCP
  • Clinical Monitoring
  • Clinical Development
  • Oncology
  • ICH-GCP
  • Pharmaceutical Industry
  • Clinical Research
  • EDC
  • Regulatory Affairs
  • Therapeutic Areas
  • Pharmacology
  • Regulatory Submissions
  • Protocol
  • Pharmacovigilance
  • GMP
  • Diabetes
  • Clinical Data Management
  • Infectious Diseases
  • See 6+  See less

Education

Cranfield University

MSc Clinical Research (Executive)

University of Portsmouth

Upper Second Class, Pharmacology

St. Columba's College

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