COVANCE NETHERLANDS CRA JOBS

Covance Netherlands offers unique job opportunities for experienced CRA I, CRA II or SCRAs within the Global Clinical Trial Operations team.

These jobs would suit CRAs who already have minimum 1,5 years independent monitoring experience in The Netherlands with international ph I-III clinical trials, within pharma or CRO environment.

• Experience monitoring ph I-III clinical trials in oncology is highly desirable for the job
• National travel within the Netherlands will be expected

These jobs offer excellent exposure to a range of disease areas and a real chance of career progression and promotion opportunities in time.

Covance is committed to the well-being and development of its CRAs and one of the values of the Dutch Clinops group is its strong Management Team and great supportive team spirit between all the colleagues.

Time and again staff comment on their amazing colleagues in Covance Clinops NL and the camaraderie of the department, with many people starting their careers or joining us, developing and remaining with us for many years.

The Dutch Management team constantly review study/site allocations and workload to actively balance with wellbeing of staff, and take actions to address where needed working closely with project teams, unlike a lot of other CROs.

Education

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)

• Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries
• Thorough understanding of the drug development process
• Fluent in Dutch and in English, both written and verbal

Experience:

These jobs would suit CRAs who already have minimum 1,5 years independent monitoring experience in The Netherlands with international ph I-III clinical trials, within pharma or CRO environment.

Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs

Advanced site monitoring skills

Advanced study site management skills

Good planning and organization skills

Good computer skills with good working knowledge of a range of computer packages