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Senior Clinical Research Associate

Covance 3/13/2019 5:53:36 PM
JOB ID: 29163 Category: Clinical Research Associates
Munich, Germany

   

 

Job Overview

Covance is searching for a SCRA to be home based in Germany, outsourced to the sponsor

Are you an organized person who can work independently and take ownership of your career? Would you like to gain on-the-job skills while helping advance life-changing medicines?

If you are looking to enter a nurturing environment that provides a clear path to advancement, consider furthering your career as a Covance Clinical Research Associate (CRA). In this role, you will:

* Support large, prominent pharmaceutical company with their clinical trials
* Have opportunity to gain Experience in monitoring oncology studies
* Oversee site monitoring with remote and in-person visits
* Work in a flexible environment with a close-knit team
* Use time management and people skills to ensure complianceWorking both field and home-based, our CRAs form strong connections with a team that works together to achieve shared success. As a CRA at Covance, you can expect to:

Why CRAs choose Covance

* Build a long-term career path as you join a CRA team where people stay for an average of 6 to 10 years
* Develop your skills through in-depth CRA training and mentoring, opening up new opportunities to further your career
* Gain exposure to studies across early clinical development to late stage trials – and explore new opportunities across outside business units
* Embrace our people-focused culture that helps you achieve a work/life balance and ensures your ability to focus on what's important to you
* Work with top-notch people as you serve as a valuable partner to clinical sites

What we're looking for

CRAs are the most successful at Covance with at least two years of clinical monitoring Experience along with:

* A university or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)
* Familiarity with following Standard Operating Procedures, ICH guidelines and GCP
* Experience conducting pre-study, site initiation, routine monitoring and close out visits
* Ability to negotiate study budgets with investigators and assist the Covance legal department with statements of agreements
* Deep understanding of Serious Adverse Event (SAE) reporting
* Therapeutic Experience including but not limited to cardiovascular, diabetes, oncology, infectious disease, neuroscience, metabolism and vaccines
* A valid driver's license

See what Covance CRAs have to say

“I work very hard but have a good balance. My manager is very supportive and in tune to my professional development.”

"I have really enjoyed working with my colleagues to accomplish project objectives and can see that what I do has an impact on the success of this company."

"Clients want to work with us. I truly believe we have quality work and quality people.”

The CRA opportunity

Beyond the excellent compensation and comprehensive benefit package you'll receive as a Clinical Research Associate, joining Covance opens the door to many career opportunities. Learn more about what's possible with a company who truly invests in you at http://covance.com/CRAcareers.

Get to know Covance

At Covance, we value your unique point of view and bold ideas to help bring innovative medicines to market and advance modern healthcare. Join our supportive team and see how our flexible work environment along with mentoring, training and career development can help you thrive personally and professionally.

Together, let's shape new possibilities for your career and improve the lives of patients around the world.

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity).

Your confidentiality and privacy are important to us.

Education / Qualifications

* Bachelor Degree in Science or comparable

Experience

* Previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits)
* Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
* Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
* Good analytical and negotiation skills
* Computer competency
* Fluent in local office language and in English, both written and verbal


Position Type: Full-Time

Location: Munich, DEU - Germany



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Covance Recruiting Process

Below is a general Overview of Our Recruiting Process

If you’d like to work for us, please submit your resume/CV online. If your ability to use or access our electronic application is limited due to a disability, please visit www.gettinghired.com or call 1-800-978-4473 for help.

We consider applications from everyone who is interested in a position with us and who meets the required criteria and qualifications.

If your application is selected, someone from our recruiting team will contact you to arrange an initial screen. We may carry this out over the phone or at a face-to-face meeting. You must complete the screen to be considered for the position.

Based on the results of the initial screen, we may invite you to an interview. One of our recruiting team members will contact you to arrange this. The process may involve several interviews, initially over the phone, and then face-to-face with different members of the hiring team.

Our interviews follow a behavioral-based format. This means we’ll ask you to give us information that’s specific to your professional and educational experiences.

Hiring team members will share and discuss their input and then make their decision.

If you’re the person who best meets the requirements of the position, a member of the hiring team will get in touch to make you an offer of employment. Covance is an eVerify employer (United States only).