Clinical Research Associate

Proclinical are recruiting for a Clinical Research Associate to join a medical technology and devices organisation. This role is on a permanent basis with the ability to work remotely in Germany.

Responsibilities:

• Perform and/or assist with centralised oversight actions.
• Uphold adherence of clinical sites to agreed recruitment plan, timetable, and quality specification.

• Produce spreadsheets, reports and/o presentations for project status reporting.
• Daily management of study to guarantee compliance, data quality and adherence to timeline, which involves site quality actions.
• Conduct all clinical site monitoring actions, inclusive of all study visit types such as SQV, SIV, IMV, CDV, etc.
• Partake in the development of study documents, tools, and materials and any other documentation for performing clinical studies.
• You will submit clinical studies to ethical committees as well as proficient authorities.
• Other duties may be assigned.

Key Skills and Requirements:

• A systematic and organised individual with the ability to resolve issues.
• Interpersonal and communication skills both verbally and in writing.
• A compliance mindset.
• Comprehension and familiarity with ophthalmology.
• Computer literacy and competency in database systems as well as eCRF (EDC).
• Fluency in the English language within a global setting with knowledge in German which would be beneficial.

Sollten Sie Fragen oder Schwierigkeiten bei der Bewerbung haben, wenden Sie sich bitte an Nico Kowles unter der +49 6958996969.

Proclinical ist eine spezialisierte Personalberatung, die berufliche Chancen in der pharmazeutischen, biopharmazeutischen, biotechnologischen und medizintechnischen Branche anbietet.

Proclinical Staffing ist außerdem ein Arbeitgeber der Chancengleichheit.

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