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Job Details

Study Delivery Administrator (CTA) - Contract – 11 months – Global Pharma

Company: Meet
Location:
Reference: CTA Top Pharma
Closing Date: 24 Dec 16
Type: Contract
Salary (£): Competitive
Benefits:

Job Summary:

I am currently working on behalf of a global pharmaceutical company looking for a Clinical Study Coordinator primarily responsible for helping with the coordination of clinical trials. The position is office based and the contract is for 11 months with a high chance of extension. This is a great opportunity for an experienced CTC/ CTA to join an internationally respected pharmaceutical company.

Requirements:

Role: Study Delivery Administrator

Location: South East

Company: Global Pharma

Contract Length: 12 months

Rate: £220

 

 

Summary

I am currently working on behalf of a global pharmaceutical company looking for a Clinical Study Coordinator primarily responsible for helping with the coordination of clinical trials. The position is office based and the contract is for 11 months with a high chance of extension. This is a great opportunity for an experienced CTC/ CTA to join an internationally respected pharmaceutical company.

 

Get in touch to discuss this role further! aman@peoplewithchemistry.com  or call me on 0203 019 5976. Your CV will be treated in complete confidence.

 

Company Profile:

My client is a well-established and well respected international leader in the pharma industry, being in the top 10 largest pharma companies worldwide and the second largest for research and development. They have a great reputation as an employer and a history of extending contracts. As a company which is steadily growing and expanding its pipeline, this would be a great opportunity for a contractor.

 

Get in touch to discuss this role further! aman@peoplewithchemistry.com  or call me on 0203 019 5976. Your CV will be treated in complete confidence.

Responsibilities:

·         Proactive participation in the UK study teams and all administrative aspects of the set up till reporting

·         Work closely with the documentation team until the clinical study report is finalised.

·         Study tracking and study documentation maintenance

·         Operational responsibility to set-up the local Trial Master File

 

Skills Required:

·         Minimum of 3 years experience within the pharma industry

·         Ethics submissions

·         R&D submissions

·         Worked in a Pharma background

 

 

Full job description and company details are available upon application, apply below. This position is being dealt with by Aman Gupta at Meet, please call on.You can also e-mail us directly at aman@peoplewithchemistry.com to discuss in confidence.

 

Meet are good people who are great at recruitment. We’re proud to partner with the industry’s leading Pharmaceutical, Biotechnology, Medical Device, Marketing Communications and Contract Research Organisations (CROs) worldwide, helping them to find and secure the best global talent available.  We pride ourselves on our open, friendly approach and are here to guide you through the recruitment process every step of the way.

 

Find out more about us at www.peoplewithchemistry.com 

 

Consultant LinkedIn page please click here.

 

Keyword: CTC, CTA, clinical trials, administrator, assistant, coordinator, pharma, oncology, associate, project associate, pharma, clinical, ethics, submissions,

 

 

 

Apply for this job: Study Delivery Administrator (CTA) - Contract – 11 months – Global Pharma

Contact Information:

Address:  meet
Euston Tower Levels 32-34 286 Euston Road London
NW1 3DP
England
Tel:  +44 203 178 7488
Website:  Visit Our Web Site

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