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Job Details

Remote Site Monitor (Central)-143559

Company: PPD
Location: Europe, Middle East & Africa-Bulgaria-Sofia-Sofia
Reference: 143559
Closing Date: 23 Mar 18
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

  PD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. ...

Requirements:

 

PD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health. For more information, visit www.ppdi.com.
Now a great opportunity exists for:
 
Remote Site Monitor/Report Review Specialist

 

Required Education and Experience:


• Life Science Degree and/or relevant qualification/experience;
• At least 3 years direct clinical monitoring experience as a clinical research associate that provides the knowledge, skills, and abilities to perform the job is required.
• In-depth understanding of ICH/GCP guidelines;
• Excellent standard of verbal and written communication skills in English;
• Highly organized with strong attention to detail and deadlines;
• Advanced skills across all of the Microsoft packages;

Qualifications

Responsibilities:

• Performs review of clinical monitoring visit reports ensuring consistency across protocols and/or regions and escalates any protocol, site, and/or CRA issues or trends noted during the report review process to CTM.

• Liaises with CRA for prompt trip report review submission and approval as per the stipulated timelines of PPD and/or the Sponsor.

• Evaluates PI oversight (e.g., protocol adherence), subject safety and study processes in order to assess site’s ability to conduct study, as ascertained from information noted in monitoring visit reports and associated electronic data systems.

• Provides trial MVR status tracking and progress update reports to CTM/CRA as required.

• May assist project manager or clinical team manager on assigned projects.”

Apply for this job: Remote Site Monitor (Central)-143559

Contact Information:

Address:  PPD Cambridge
Granta Park
Great Abington
Cambridge

CB21 6GQ
England
Website:  Visit Our Web Site

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