Job Overview :
Are you ready to discover you next career at Covance?
A career at Covance provides our employees the unique chance to create an immediate impact and difference in our patient’s lives.
Joining Covance Flexible Solutions (FSPx) will offer a rewarding career, a chance to work in an energetic & 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.
Joining Flexible Solutions (FSPx) you will have :
The opportunity to work across multiple therapy areas and global trials.
The option to move your career between Covance Lead trials and CoSource.
To receive ongoing training and support provided by both the Client and Covance dedicated Clinical Operations Manager.
The opportunity to join a global CRO requiring the best and brightest CRA talent to join and make a difference
One set of Client SOPs and see trails run from a pharmaceutical viewpoint
Our mission is to help our clients bring the miracles of medicine to market sooner join us for your next career move.
Education / Qualifications :
Minimum Required :
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)
Basic knowledge of Regulatory Guidelines
Basic understanding of the clinical trial process
Fluent in local office language and in English, both written and verbal
Working knowledge of Covance SOPs regarding site monitoring
Experience : Minimum Required :
Minimum Required :
2 years experience in a related role (e.g. site management, in-house CRA, study coordinator, research nurse, etc.)
Basic understanding of Regulatory Guidelines
Ability to work within a project team
Good planning, organization and problem solving skills
Good computer skills with good working knowledge of a range of computer packages
Works efficiently and effectively in a matrix environment
Valid Driver's LicensePreferred :
Two or more year's additional experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred
2 years on site monitoring experience (Unblinded experience preferred).
Oncology TA experience.