Emplois actuels liés à Clinical Research Associate Trainee - Paris, Île-de-France - IQVIA
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il y a 5 jours
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il y a 4 semaines
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il y a 4 semaines
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Il y a 2 mois
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il y a 2 semaines
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Experienced Clinical Research Associate
il y a 1 mois
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Senior Clinical Research Associate
il y a 2 semaines
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Senior Clinical Research Associate
il y a 1 semaine
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Freelance Clinical Research Associate
il y a 1 semaine
Paris, Ile-de-France Meet Temps pleinJob Title: Freelance Clinical Research Associate (CRA) – Full-Time Location: Remote/France Job Type: Full-Time Freelance (FTE 1.0)Job Description: We are seeking an experienced Freelance Clinical Research Associate (CRA) for full-time engagement to manage oncology-focused clinical trials. This is an opportunity for someone with extensive experience in...
Clinical Research Associate Trainee
Il y a 2 mois
Overview: The IQVIA Research and Development Solutions team is dedicated to assisting healthcare clients in discovering innovative treatment options for patients facing various health challenges, whether common or rare. This internship offers a unique opportunity to participate in a comprehensive training program designed to equip you with the necessary knowledge and skills to conduct clinical monitoring visits independently, adhering to study protocols, standard operating procedures, good clinical practices, and relevant regulatory standards.
Key Responsibilities:
- Complete necessary training in therapeutic areas, protocols, and clinical research to fulfill job responsibilities.
- Gain hands-on experience in study procedures by collaborating with seasoned clinical professionals.
- Under close supervision, execute site selection (if applicable), initiation, monitoring, and closure visits in line with the contracted scope of work and good clinical practices.
- Administer protocol and related study training to assigned sites while establishing consistent communication to manage project expectations and address issues.
- Evaluate the quality and integrity of study site practices concerning protocol adherence and applicable regulations, escalating quality concerns as necessary.
- Track the progress of assigned studies, including regulatory submissions, recruitment and enrollment, Case Report Form (CRF) completion, and data query management, with potential support during the start-up phase.
- Create and maintain accurate documentation related to site management, monitoring visit findings, and action plans, including regular visit reports and follow-up correspondence.
- Collaborate with study team members to support project execution as needed.
Qualifications:
- Bachelor's degree, preferably in healthcare or a scientific discipline.
- Proficient written and verbal communication skills in English.
- Competent in computer applications, including Microsoft Word, Excel, PowerPoint, and Outlook.
- Strong organizational and problem-solving abilities.
- Effective time management skills.
This internship is an excellent opportunity to contribute to the life sciences industry while developing your professional skills in a supportive environment.
About IQVIA: IQVIA is a premier global provider of advanced analytics, technology solutions, and clinical research services tailored for the life sciences sector. We are committed to advancing human science and data science to create a significant impact, ultimately aiding our clients in fostering a healthier world.
