Senior Clinical Research Associate I - London, United Kingdom - Caidya

Caidya
Caidya
Verified Company
London, United Kingdom

2 weeks ago

Tom O´Connor

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Tom O´Connor

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Description

Job Title:


Senior Clinical Research Associate I

Job Location:
London, United Kingdom

-
(Home-based, any UK location considered)

Job Overview:


Job Duties and Responsibilities:


  • Provides support to Project Team and Clinical Operations Team.
  • Maintains strong working knowledge of protocols and Monitoring Plans for assigned projects.
  • Demonstrates strong written and verbal communication skills.
  • Serves as primary contact for assigned research sites.
  • Verifies that the investigator, staff, and site facilities remain adequate throughout the trial period.
  • Responsible for the scheduling and conduct of prestudy visits, initiation visits, interim monitoring visits and closeout visits according to the Monitoring Plan.

Supervisory Responsibilities:

No supervisory responsibilities.


Job Requirements:


  • Education
  • 4year college graduate, preferably with a healthcare or life science degree.
  • Experience
  • Minimum of 3 years of experience in onsite monitoring of clinical studies
  • Monitoring experiences in several different indications and study types
  • Experience
in all areas of monitoring (on-site, remote, etc.)

  • Skills/Competencies
  • Strong written and verbal communication skills
  • Strong interpersonal skills
  • Expert monitoring skills to independently conduct all types of site monitoring visits
  • Good documentation skills; good command of English and the local language in the area of activity (reading, writing, understanding)
  • Comprehensive knowledge of GCP/ICH guidelines
  • Capabilities
  • Ability to drive an automobile and have a valid driver's license, if applicable.
  • Valid passport required in the case of international business travel.
  • Ability to travel up to 80%.
LI-MY1

The company will not accept unsolicited resumes from third-party vendors.

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