Clinical Research Associate
il y a 1 semaine
Responsibilities:
- Conduct source data verification in compliance with the needs as set out in the monitoring manual.
- You will verify whether safety reporting needs are met such as SAE, SUSAR, line listings, etc.
- Organise discussions between site personnel and any other party.
- When able, work in a proactive/predicting manner to avert issues from occurring.
- Contribute to divisionwide duties to partake in the optimisation of procedures within the division.
- Plan, perform and document site selection, initiation, supervision and closeout visits.
- Other duties may be assigned to this role.
Skills & Requirements:
- Educated to a degree level in a life science division, ideally higher vocational training or academic degree.
- At least 1 year of experience within global clinical research
- Fluency in the English Dutch and French languages with knowledge in an additional European language would be beneficial.
- Computer literacy in Microsoft Office such as PowerPoint, Outlook, Word and Excel as well as any other systems.
- Knowhow of ICH-GCP and all suitable regulatory needs.
- A diplomatic and methodical individual.
- Communication skills both verbally and in writing.
- Works well independently and in a team with the ability to be analytical and resolve issues.
- An organised individual with a high attention to detail and is precise.
- Capable of being stress tolerant.
- Willing to travel for business needs.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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