Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Pharmiweb.com RSS Feed PharmiWeb Candidate Blog

Pharmiweb.com RSS Feed PharmiWeb Client Blog

Job Details

CRA II or SCRA Denmark

Company: Docs Global (Continental Europe)
Location: Copenhagen,Denmark
Reference: Ref AS-020175
Closing Date: 27 Feb 17
Type: Permanent
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

Why Apply This position is with a market leading Clinical Research Organisation who is known for their high quality of service to clients. To express your interest and to find out more about the role, please send your CV today to Claudia.JorgensenRankine@docsglobal.com. *Applicants who have not had a response within two weeks should assume their application has been unsuccessful.

Requirements:

Roles & Responsibilities of the position

You will perform and coordinate all aspects of the clinical monitoring process including: - Monitoring Clinical studies from start-up to close-out with full-site management responsibility - Identify site needs and site-related issues, escalate and/or initiate corrective actions when necessary, providing solutions for site staff to facilitate the clinical trial process - Respond to site-related queries and escalate issues if necessary to the leadership team - Perform investigational product accountability and reconciliation, maintain site study supplies and facilitate the resolution of clinical queries to investigative staff - Build and maintain successful and long-term relationships with investigators and site staff - Ensure clinical study sites are conducting clinical trials in compliance with the respective protocol, client’s SOPs and applicable ICH/GCP guidelines and regulations - Assist in preparing sites for audits, review audit reports and contribute to resolving findings - Contribute to training of new joiners and assisting by participating in co-monitoring visits

Job Requirements

Qualifications: •A minimum of 10 months on site monitoring experience •University degree in a science related field or are a certified health professional •In depth knowledge of ICH-GCP, EU and FDA requirements •Experience of clinical trials •Willingness and ability to travel •Excellent English/Danish language skills

Remuneration & other details

What is Offered: The successful candidates can look forward to job stability with a leading CRO that has experienced year-on-year growth. They offer a generous salary and benefits package as well as excellent learning and development opportunities. They understand that the best CRAs are not necessarily on their doorstep, so if you are looking for a home based role they can offer this option too, providing everything you need to fulfill your potential from your home office.

Apply for this job: CRA II or SCRA Denmark

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Marlow
Buckinghamshire
SL7 1HZ
England
Website:  Visit Our Web Site

Advertising
Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.