Icon - Cra Be - Berlin - Brussels, België - Meet Recruitment
Beschrijving
55000 EUR EUR- Brussels, Belgium
- Permanent
_ 1.
Position:
Clinical Research Associate I (CRA I) - 53K average salary_
Our client, a leading Clinical Research Organization (CRO) ranked among the top 10 globally, is actively seeking a talented and motivated Clinical Research Associate I to join their dynamic team in Belgium.
Key Responsibilities:
- Conduct onsite monitoring visits in accordance with the study protocol, GCP, and regulatory requirements.
- Ensure data accuracy, patient safety, and protocol compliance.
- Build strong relationships with investigative sites and collaborate with crossfunctional teams.
- Assist in the preparation and review of essential study documents.
Qualifications:
- Bachelor's degree in a related field.
- Minimum of 12 years of clinical research experience.
- Knowledge of GCP and regulatory guidelines.
- Strong communication and organizational skills.
- 2.
Position:
Clinical Research Associate II (CRA II) - 62K average salary_
Join our client's esteemed team as a Clinical Research Associate II and take your career to the next level. This position offers the opportunity to work on cutting-edge clinical trials, ensuring the highest quality in clinical research.
Key Responsibilities:
- Perform onsite monitoring, site management, and closeout visits.
- Ensure compliance with study protocols, GCP, and regulatory requirements.
- Develop and maintain strong relationships with investigative sites.
- Contribute to the success of earlyphase trials from initiation through completion.
Qualifications:
- Bachelor's degree in a related field.
- Minimum of 23 years of clinical research experience.
- Proficiency in using clinical trial management systems.
- Excellent communication and interpersonal skills.
- 3.
Position:
Senior Clinical Research Associate (Senior CRA) - 73K average_
Our client is actively seeking a Senior Clinical Research Associate to play a key role in the success of their clinical trials.
This is an excellent opportunity for an experienced professional to contribute to impactful projects and grow within a globally recognized organization.
Key Responsibilities:
- Lead, motivate, and develop team members.
- Manage evidence dissemination with regional alignment to commercial partners.
- Maintain extensive clinical/scientific expertise in relevant therapeutic areas.
- Collaborate with crossfunctional teams to execute field team strategic plans.
Qualifications:
- Advanced degree in a related field.
- 5+ years of relevant independant CRA experience.
- Strong knowledge of GCP, regulatory guidelines, and medical device development.
- Ability to travel nationally and internationally.
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