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Clinical Research Associate - South Africa

Covance 3/13/2019 5:53:43 PM
JOB ID: 29300 Category: Clinical Research Associates
Centurion, South Africa

   

 

Job Overview

Discover new opportunities to grow your career as a Covance FSP Clinical Research Associate.

Covance FSP are looking to hire a Clinical Research Associate in South Africa, Johannesburg. In this position you will be fully dedicated to our sponsor and you will be working home based.

At Covance, you can redefine what is possible and discover your extraordinary potential within our Functional Service Provider team (FSP).

As a Covance employee dedicated to an FSP project you will bring your specialized discipline to a core team working directly with one sponsor. Whether your specialization is in clinical monitoring, clinical project management, data management, biometrics or pharmacovigilance Covance has an FSP opportunity to match your area of expertise.

Each FSP offers a unique opportunity to be a part of the drug development cycle and see a product through to launch. We have multiple partnerships giving you the variety and the flexibility to stay with sponsors, try a new external secondment or work in house on Covance studies.

With the support of exceptional people and an energized purpose, you'll be empowered to own your career journey with dedicated mentoring, training and personalized development planning.

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

* 4 year degree in life sciences and related fields

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).


Position Type: Full-Time

Location: Centurion, ZAF - South Africa



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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).