Site Identification & Qualification: Researching and identifying new sites and evaluating previously used sites in order to collect a realistic assessment of a site’s enrollment potential. Responsibilities include:
- Participating in the identification of new study centers, including gathering basic contact information and capabilities.
- Participating in the site qualification/validation process.
- May evaluate site qualification for general site viability.
- Works with the site to develop realistic enrollment targets.
- Working with Clinical Resource Organization (CRO) monitors, as appropriate.
- Providing solutions to increasingly complex problems.
- Suggesting solutions that are appropriate, innovative and practical.
- Providing training and/or guidance to site personnel.
- Applying and promoting best practices.
- Participating in mentoring Clinical Research Assistants and/or other CRAs.
- Participating in professional meetings, symposia, and conventions to maintain competencies.
- Developing contacts and relationships with peers.
- Engaging in discussions surrounding projects to share experiences and knowledge.
- Taking initiative for personal and professional development.
| De eisen
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The recommended skills and qualifications for the CRA position include a Bachelor of Science degree in a relevant field combined with some experience in pharmaceutical industry clinical trials. Travel is a requirement in order to ensure the appropriate monitoring of sites in accordance with the Monitoring Plan.
| | Contactinformatie
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Heb je interesse in deze vacature, meld je direct aan middels de button 'aanmelden' of neem contact op met:
Drs. Andrea Dorssers
Consultant Clinical
Biltstraat 443
3572 AW Utrecht
tel 030 231 7350
mobiel 06 22242929 |
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Geïnteresseerden kunnen hun c.v. ook rechtstreeks mailen naar andrea@pharmamediair.nl.
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