Covance Clinical Research Associate (ad) in Munich, Germany

Job Description:

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

Requisition ID: 57780BR

Job Category: Clinical Research Associate

Locations: Germany - Munich

Shift: 1

Job Postings: 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 Statement:

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.