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Job Details

Clinical Research Associate - Sponsor

Company: Hobson Prior
Location: Surrey
Reference: IQX-665632
Closing Date: 23 Jan 17
Type: Permanent
Salary (£): On Application
Benefits: £35-50,000

Job Summary:

Overview: My client is a growing international specialist healthcare company who’ mission is to bring to market, medical products that meet the needs of specialist healthcare physicians and their patients.

Requirements:

Overview: My client is a growing international specialist healthcare company who’ mission is to bring to market, medical products that meet the needs of specialist healthcare physicians and their patients.

They are currently seeking a CRA to work for their Medical Devices subsidiary in the UK. The position is permanent, full time and located in the South East of England.

Responsibilities include:

·         Ensure that the conduct of the trials are in compliance with the currently approved protocol/amendments, with ICH current GCP, FDA, CFR along with other applicable Sponsor and regulatory requirements.

·         Conduct on-site clinical monitoring that includes but is not limited to; protocol training as required, trial document review, ensuring accurate data acquisition and recording, monitoring adverse events, concomitant medications and verifies they are reported in accordance with the protocol on the electronic Case Report Form (eCRF), verification of subject data, ensuring adherence to the clinical protocol, site and Sponsor SOPs,

·         Monitor and complete regular investigational product accountability, verification of product shipping/storage conditions.

Requirements:

·         A degree in health care, biological sciences, or equivalent along with experience in the medical device and/or pharmaceutical environment monitoring clinical sites and working with clinical professionals within a team.

·         Must possess on-site monitoring experience including Electronic Data Capture (EDC) studies.

·         Excellent oral, written, analytical, and interpersonal skills along with solid computer tracking capabilities to manage and meet project goals within expected timelines and study metrics.

·         Effective and proven clinical monitoring skills.

·         Effective organizational and time management skills.

·         Proven flexibility and adaptability, willingness to travel 40%

·         Ability to work independently as required.

·         Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software.

Apply for the role of Clinical Research Associate using the form below, or contact us for more details.

 

 

 

 

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Contact Information:

Address:  Hobson Prior International Ltd
Wellington Gate
7-9 Church Rd.
Tunbridge Wells
kent
TN1 1HT
England
Tel:  01892 612 612
Fax:  01892 612 613
Website:  Visit Our Web Site

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