Covance by LabCorp are helping to develop what could be the first pharmacological treatment able to help 3+ million severily ill hospitalized patients worldwide... and we need you to contribute with your expertise .

Saving lives, advancing medicine. Weren´t these the main reasons you became a CRA in the first place?

COVANCE by LabCorp

With all the uncertainty in the world, your job stability should not be a concern.

Covance have supported the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today. But we are much more than a normal CRO:

• We are also the world´s biggest Central Lab, generating more clinical trial data than all other central laboratories combined
• Our Early Phase Solutions have proved to shave off 30 % time from lead candidate to Proof of Concept
• LabCorp/Covance were the first in receiving FDA approval to perform COVID19 tests using an at-home collection kit.

Join us and see why Covance are uniquely positioned to offer you not only a job, but a stable, long-term international career, and why more than 90% of the top 20 global pharmaceutical companies are repeat customers.

THE JOB

For a strategic project in the UK, we have opened 2 jobs at CRA II and SCRA levels.

For these jobs we can only consider experienced CRA II or SCRA who have monitored ICU/ Critical Care trials or have former ICU/ Critical care nursing experience .

• Both are permanent jobs with Covance
• Location: You can be home based anywhere in the UK, or office based in Maidenhead / Edinburgh
• You would be monitoring across intensive care units (ICU) within the main hospital centers in the UK.

IS THIS YOU?

We don´t hide you will work in a complex and demanding protocol, but we know that this new treatment´s scientific challenge will keep you hooked to the team.

At Covance we trust our CRAs and so we will give you autonomy to organize your work. In turn, we expect you to go beyond the typical CRA role and really be an expert of your protocol and to own your sites .

• Your focus will be direct site management and we expect you to influence site performance

• We need your hands-on experience nurturing a collaborative relationship with your ICUs: how will you make the study relevant for them, amidst all the speed, the plethora of alarms coming out of all types of equipments, the life and death decisions?

• How will you efficiently solve their issues and answer their questions about systems, documentation, filing or building audit-ready habits?

APPLY NOW

... so we can tell you about the cookies & brownie days, the sense of humor and team support that permeate everything we do, how our managers constantly review study/site allocation to ensure workload balance or why you will not grow a stale career with us

Education/Qualifications:

University life science degree or Nursing background.
Experience:
For these jobs, we can only consider:

• CRA II or SCRA who have monitored Intensive Care Unit / Critical Care trials in the UK, or
• CRA II / SCRA who have former ICU/Critical care nursing or study coordinator experience in the UK
• Excellent understanding of Serious Adverse Event (SAE) reporting