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Senior Regulatory Submissions Associate

Covance 11/7/2018 2:37:53 PM
JOB ID: 24057 Category: Regulatory
Maidenhead, United Kingdom

   

 

Job Overview

Job Summary

Covance is expanding and is looking to recruit a Senior Regulatory Submissions Associate to join the team at our Maidenhead office. The role is responsible for the timely preparation of submissions to Regulatory Authorities in support of investigational and marketed products. You will Interact with Regulatory Authorities and with clients to support regulatory activities. Proactively interact with other Covance groups and clients to provide guidance regarding Regulatory Authority requirements and project timelines and requirements. Working with minimal supervision, it is the responsibility of the Senior Regulatory Associate to prepare documents to the required standard and to maintain awareness of current regulatory standards related to submissions for drug and biologic products. This role may also have have supervisory responsibilities.

A career at Covance provides our employees the unique chance to create an immediate impact and difference in our patient's lives. Joining Covance will offer a rewarding career, a chance to work in a high-energy & team oriented work place, and access to competitive benefits. With the support of exceptional people from across the globe and a vast array of career options, you'll be empowered to own your career journey with mentoring, training and personalized development planning. As a Covance employee, your work will be meaningful, the patient outcomes are real, and the results are lasting.

Our mission is to help our clients bring the miracles of medicine to market sooner -- join us for your next career move.

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

Recommended:

Bachelor's Degree in Life Sciences or equivalent.

Experience

* Candidates should have excellent communication skills, organization and planning skills and have high attention to detail.
* Must have a wealth of Experience in the pharmaceutical industry within regulatory affairs or drug development


Position Type: Full-Time

Location: Maidenhead, UK - United Kingdom



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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).