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Site Manager / In-House CRA

Avania

Bilthoven, Utrecht, NetherlandsRemoteJobNo compensation foundTracked 3 days agoSeen in employer's feed 3 days ago
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At a glance

Compensation
No compensation found
Location
Bilthoven, Utrecht, NetherlandsRemote
Work Authorization
Not specified

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Avania is hiring a Site Manager (In-House CRA) as an entry‑level role within the Clinical Operations team, offering training to become a travelling CRA and providing opportunities for professional growth in a fast‑growing MedTech environment.

Skills & qualifications

RequiredNice to have

Skills

Clinical Trial MonitoringStudy Specific DocumentsCommunication and MeetingsGCP ICH E6 KnowledgeFDA Regulations KnowledgeISO 14155 KnowledgeISO 13485 KnowledgeISO 9001 KnowledgeMedical Device Regulatory KnowledgeUnderstanding Medical DetailsFluent EnglishCustomer FocusCollaborationCommunicates EffectivelyResourcefulnessDecision QualityPlanning and AlignmentTravel Ability

Qualifications

B.a./B.S. Or Equivalent1 Year Clinical Research Experience PreferredFluent English

Full job description

Avania is hiring - Site Manager (In-House CRA)

The Site Manager role is an entry level position, similar to that of an In-House CRA in to the Clinical Operations team with exciting prospects, training and development to become a travelling CRA

The Site Manager (In-House CRA) role involves being trained on all basics in regards to the execution of a clinical research project. Site Managers (In-House CRA) should be able and can be asked to perform any Clinical Trial Associate (CTA) activities, which will include;

  • Clinical Trial Monitoring

  • Study-Specific Documents and Files

  • Communication and Meetings

Candidates who offer a combination of the skills, knowledge and experience listed below are encouraged to apply for Avania's Site Manager (In-House CRA) opportunity. With our continued growth we are hiring talent to join us on our journey and grow with us.

We seek -

  • B.A./B.S. or equivalent experience in a (para)medical, scientific or health related discipline or related work experience

  • Minimum of 1 year of relevant work experience in clinical research is preferred, in particular as a Clinical Trial Associate (CTA) or Clinical Research Associate (CRA)

  • Ability to understand basic and complex medical details

  • GCP-ICH-E6, FDA regulations and ISO 14155, 13485 and 9001 knowledge where applicable

  • Knowledge of regulatory regulations and guidelines on medical devices

  • Ability to travel domestically and internationally

  • Fluent English, spoken and written

  • Customer Focus

  • Collaboration

  • Communicates Effectively

  • Resourcefulness

  • Decision Quality

  • Plans and Aligns with Key tasks and responsibilities

We offer -

  • The opportunity to work in an innovative, fast-growing and rewarding industry

  • A dynamic and enthusiastic global team that fosters collaboration and the opportunity to work with experts across many specialties

  • Exchange of knowledge and ideas to help employees grow and advance their careers, backed with training and other development opportunities

  • Competitive compensation and benefits package (details shared during the interview process)

  • Some roles offer the opportunities for travel

  • Ask us about our hybrid and fully remote work opportunities

Avania - MedTech's trusted Champion

We look forward to receiving your application!

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