• Covance
  • Concord , NH
  • Education - Excluding Post Secondary
  • Full-Time
  • 322 N State St

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**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!**
**This can be a remote role if you do not live in the** **Indianapolis Metropolitan Area.**
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** **p** **eople** **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
**Job Number** _2018-19961_
**Job Category** _Clinical Operations Entry Level_
**Position Type** _Full-Time_
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.
Associated topics: admission, administrative assistant, advocate, attendance, clinician, pathologist, registration, school clerk assistant, secretary, student affairs

* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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