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Job Details

COVANCE GERMANY - hires experienced CRAs, all levels of seniority!

Company: Covance
Location: Germany
Reference: 57780BR
Closing Date: 07 Dec 16
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

COVANCE GERMANY - hires experienced CRAs, all levels of seniority! Location: office based Munich or field based across Germany

Requirements:

Clinical Research Associate, CRA, full-time. 

Do you know Covance is one of the most stable, fastest growing global Contract Research Organization? 

For example, our Clinical Development teams have supported the development of one-third of all prescription medicines in the market today and of 47 out of the 50 best-selling oncology drugs. 

The work we do at Covance impact the lives of millions of people around the world… so could you too as our next: 

Clinical Research Associate, all levels of seniority: CRA I, CRA II, Sr CRA 

Can you bring your drive to our cutting-edge clinical projects? 

We need experienced CRAs who are ready to apply their pre-study, initiation, monitoring and closeout visits expertise, and their deep ICH-GCP and SAE management expertise to bring safe, effective and essential medicines to market sooner. 

Location: office based Munich or field based across Germany

Education/Qualifications

Our ideal person is someone who… 

• Has a University degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology, Medizinischer Dokumentar)

Experience

Our ideal person is someone who… 

• Has previous clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits) in international, ph II-III, sponsor initiated trials. We are especially interested in candidates with previous experience monitoring oncology trials. 
• Brings a thorough knowledge of ICH Guidelines and GCP, a basic understanding of regulatory requirements and thorough knowledge of monitoring procedures 
• Is able to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines 
• Has a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs 
• Good planning, organization and problem solving abilities 
• Good communication and interpersonal skills 
• Available for travel up to 60% of the time, including overnight stays as necessary 
• Must be fluent in German and English 
• Valid driving license

EEO Employer

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us.

Apply for this job: COVANCE GERMANY - hires experienced CRAs, all levels of seniority!

Contact Information:

Address:  Covance- Brussels


Belgium
Tel: 
Fax: 
Website:  Visit Our Web Site

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