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CRA II - Senior CRA - Clinical Operations - Turkey

Covance 4/15/2019 6:08:48 AM
JOB ID: 29947 Category: Clinical Research Associates
Istanbul, Turkey

   

 

Job Overview

Get ready to redefine what's possible and discover your extraordinary potential at Covance. Here, you'll have the opportunity to personally advance healthcare and make a difference in peoples' lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you'll be empowered to own your career journey with mentoring, training and personalized development planning.

Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients—and your career.

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We have an exciting opportunity available to join our team.

We are currently recruiting CRA II - SCRA in Turkey in Clinical Operations team. This is a regular full-time position.

Responsibilities include:

* All details of site management as prescribed in the project plans
* Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks
* Negotiation of study budgets with potential investigators and collaboration with Covance legal department with statements of agreements
* Serious Adverse Event (SAE) reporting, production of reports, narratives and follow up of SAEs.
* Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systems

Education / Qualifications

* University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)

Experience

* Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
* Previous Experience in monitoring studies in oncology area preferred
* Excellent understanding of Serious Adverse Event (SAE) reporting
* Ability to resolve project-related problems and prioritize workload for self and team
* You have previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits).


Position Type: Full-Time

Location: Istanbul, TUR - Turkey



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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).