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Study Design Lead

Covance 4/3/2019 6:12:19 PM
JOB ID: 19961 Category: Other
Regional, Nationwide

   

 

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.

Covance is looking to hire a Study Design Lead - Remote Opportunity!

Play a pivotal role in the drug development process and grow your career

Are you interested in making an impact through your everyday work? Are you passionate about advancing your career while making a difference in patients' lives? Do you love to organize projects and thrive in a dynamic, high-paced environment?

If you said yes to these questions and you are looking for a place where you can explore a multitude of career paths across the drug development spectrum, consider working at Covance as a Study Design Lead. This is a permanent, full time position, based in our Indianapolis office or it can be remotely based.

As a Study Design Lead, you will collaborate with our pharmaceutical company clients to review clinical protocols, define the components of clinical trial study designs, and work with internal teams to highlight risks and financial impacts associated with various study design options. In this position, you will be responsible for the following:

* Takes the lead to accurately interpret and translate protocol requirements in to SOW document
* Leverages technical, therapeutic area, client and Covance process knowledge to provide a comprehensive and complete SOW document
* Liaise with internal departments to understand Covance capabilities and assess feasibility of requests in order to meet client needs related to study design
* Demonstrates strong knowledge of Covance processes and technical capabilities
* Acts as a consultant to the client to advise on study design choices and works with GSM to highlight risks and budget impacts associated with study design
* Displays strong interpersonal and communication skills that will build strong relationships (internal and external) to ensure high quality study design
* Coordinates internal processes and communications related to study design (including but not limited to: internal feasibility requests, material transfer agreements and supply forecasting) and ensures the eventual follow up is integrated in to the SOW and global monitoring plan; Performs quality self-review
* Ensures that all customer requirements with relation to study design are documented and acted upon
* Able to act efficiently in an environment with dynamic timelines and priorities
* Displays appropriate self organization and ability to manage conflicting priorities
* Participate in functional meetings (eg. CLFs) and provide input, keeping processes up to date
* Comply with CCLS Global Project Management strategy
* Support a culture of continuous improvement, quality and productivity

What we're looking for in you

Do you have the following education and Experience ?

* Bachelor of Science degree (flexible to consider those without a degree that have significant related Experience )
* Minimum of 3 years of study design Experience (can include clinical database design)
* Minimum of 2 years of Experience interpreting and translating clinical protocols
* Technical writing Experience is desirable
* Experience managing Clinical Trial Projects or designing clinical databases is a plus

Why people choose to work at Covance

"At Covance, it's our people that make us great – it's what our clients, our partners and, most importantly, what our employees say. Here, you'll have the opportunity to work with extraordinary people with diverse viewpoints. You'll discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond."

Get to know Covance

Covance, the drug development business of LabCorp, is the world's most comprehensive drug development services company. Because of our broad Experience , from early research to commercialization, our more than 20,000 employees from across the globe are in a unique position to supply insights that go above and beyond testing. Our team's impact on healthcare is remarkable. Through their everyday work they've supported 100% of the top 50 drugs on the market and all the oncology drugs approved in 2016. Even though we span multiple businesses, we operate as one, sharing our knowledge to improve our efficiency and deliver on the promise of a healthier world.

The Covance team is driven by an energized purpose to improve health and improve lives across the globe. Here, you'll work alongside exceptional people who each play an important role in bringing new scientific discoveries and therapeutic area advancements to life. And, because we span the drug development spectrum, you'll directly impact a wide-range of initiatives as you explore unique career paths and discover your extraordinary potential.

Get ready to make a difference as we speed the delivery of groundbreaking therapies and improve lives of countless individuals.

EEO Statement

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 of Science degree preferred(flexible to consider those without a degree that have significant related Experience )
* High School diploma required

Experience

* Minimum of 3 years of study design Experience (can include clinical database design)
* Minimum of 2 years of Experience interpreting and translating clinical protocols
* Technical writing Experience is desirable
* Experience managing Clinical Trial Projects or designing clinical databases is a plus


Position Type: Full-Time

Location: Regional, NAT - Nationwide



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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).