Clinical Trials and Administration Coordinator

Recruiter
Experis
Location
Amersham, UK
Salary
Competitive
Posted
16 Sep 2019
Closes
25 Sep 2019
Ref
1265307281
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Clinical Trials and Administration Coordinator
  • Location: Amersham
  • Duration: 6 Months
  • Rate: Competitive

Clinical Research Trials Coordinator job opportunity based in Amersham for a global organisation, which provides transformational medical technologies and services to meet the demand for increased access, enhanced quality and more affordable healthcare around the world.

As a Clinical Research Trials Coordinator, you will join a busy Operations Team to assist in managing the lifecycle of all supported Investigator Sponsored Trials. You will proactively manage all aspects of study-related support across all brands and review documentation to verify that all research operates within global/regional regulations and complies with guidelines.

The successful Clinical Research Trials Coordinator candidate will have a background in clinical trials, research and governance. As a Clinical Research Trials Coordinator, you will have strong knowledge of clinical trial and research governance as well as the ability to multi-task and carry out tasks accurately and in a timely manner.

Clinical Research Trials Coordinator Key Responsibilities:
  • Support business objectives by facilitating trial review processes
  • Effectively communicate the decisions by establishing follow-up meetings with key stakeholders.
  • For approved studies assist the IST Responsible Person to ensure relevant workflows are processed
  • Review supporting documentation for compliance and alignment to ISTC decisions
  • Track progress against key milestones via organisational tools including databases, budget tracker, PUT Tool.
  • Build and expand relationships with internal and external customers
  • Review invoices for alignment to milestones and obtain proof of milestone achievement.
  • Review workflows relating to milestone funding and product supply for accuracy
  • Manage information requests from internal and external customers
  • Continuously monitor Mailbox and FOC (free-of-charge) confirmations mailbox and respond to queries and issues received.

Clinical Research Trials Coordinator Candidate Criteria:
  • Strong coordination, administration and customer service experience
  • Clinical / Pharmaceutical trial and research background
  • Ability to discuss good clinical practice guidelines
  • Invoicing experience
  • MS Office experience including PowerPoint, Word and Excel
  • Attention to details along with the ability to multi-task

Please submit your CV in the first instance or call Emma Jones on 07483128595.

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