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Clin Res Assoc II

Covance 6/25/2018 6:34:34 PM
JOB ID: 21566 Category: Clinical Research Associate
Regional, Israel

   

 

Job Overview

We are currently looking for talented Clinical Research Associates to join our team in Israel . You would be working within our Flexible Solutions department dedicated to one sponsor/client.

Would you like to work for one of the best known big pharma companies? Our sponsor is a global mid sized pharma company with high working standards. Are you passionate about growing in Clinical Field? We are proud to have an excellent team of the best professionals on the market and are looking for people who are ready to show true performance and interest in Clinical Trials. Do you like responsibilities and challenges? As a Clinical Research Associate you will lead all aspects of study site monitoring according to Covance SOP, ICH guidelines and GCP. You will take part in pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files.

You will become a part of our team who is always ready to help. We offer a home based position so you will not spend time on unnecessary travels but at the same time we highlight a true live relationship between colleagues. You will have a possibility to devote all your professional skills and knowledge into monitoring investigational sites as we organize our work environment and responsibilities with high standards.

Our sponsor invests heavily in training and crafts modern system of Clinical Trials so if you are passionate about working with a phenomenal team and expand your horizons feel free to reach us.

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 cooperation 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

Education / Qualifications

* University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)
* Minimum of 2 years of on-site Clinical Monitoring Experience
* Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements
* Thorough knowledge of monitoring procedures
* Basic understanding of the clinical trial process

Experience

Experience

* Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
* 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).

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.


Position Type: Full-Time

Location: Regional, ISR - Israel



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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).