Emplois actuels liés à Clinical Research Associate Trainee - Paris, Île-de-France - IQVIA
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il y a 3 semaines
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Senior Clinical Research Associate
il y a 5 jours
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Senior Clinical Research Associate
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Clinical Research Associate II
il y a 4 semaines
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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 4 semaines
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il y a 4 semaines
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Clinical Research Associate Intern
Il y a 2 mois
Paris, Île-de-France IQVIA Temps pleinIQVIA: Advancing Human and Data Science for a Healthier WorldAs a global leader in health data and technology, IQVIA provides comprehensive services to the healthcare industry across 140 countries. We leverage our extensive databases, expertise, and cutting-edge analytical tools to deliver impactful consulting solutions to stakeholders within the healthcare...
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il y a 3 semaines
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Clinical Research Associate II
il y a 2 semaines
Paris, Île-de-France Parexel Temps pleinAbout this roleParexel is seeking a Clinical Research Associate II to support oncology studies in France. This home-based position will be dedicated to a single sponsor, allowing for a high level of focus and expertise.As a Clinical Research Associate II, you will be responsible for all site management and monitoring activities across assigned studies. You...
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il y a 3 semaines
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Experienced Clinical Research Associate
il y a 1 mois
Paris, Île-de-France Pharmiweb Temps pleinJob Title: Experienced Clinical Research AssociateWe are seeking an Experienced Clinical Research Associate to join our Clinical/ Country Operations team in France. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success.Key Responsibilities:Completion of monitoring reports and follow-up letters,...
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Senior Clinical Research Associate
il y a 2 semaines
Paris, Île-de-France Parexel Temps pleinAbout the RoleParexel is seeking a Senior Clinical Research Associate to join our team in France. As a key member of our clinical research team, you will be responsible for managing and monitoring clinical trials across assigned oncology studies.Key ResponsibilitiesManage site relationships and ensure compliance with regulatory requirementsConduct on-site...
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Senior Clinical Research Associate
il y a 3 semaines
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Clinical Research Associate
il y a 3 semaines
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Senior Clinical Research Associate
il y a 1 semaine
Paris, Île-de-France Parexel Temps pleinAbout the RoleParexel is seeking a Senior Clinical Research Associate to join our team in France. As a Senior Clinical Research Associate, you will be responsible for site management and monitoring activities across assigned oncology studies.Key ResponsibilitiesManage and monitor clinical trials in oncologyWork with industry leaders and subject matter...
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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 3 mois
Overview: The IQVIA Research and Development Solutions team is dedicated to assisting healthcare clients in discovering innovative treatment options for patients suffering from various illnesses, whether common, widespread, 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 independently conduct clinical monitoring visits in alignment with study protocols, standard operating procedures, good clinical practices, and relevant regulatory requirements.
Key Responsibilities:
- Complete essential training in therapeutic areas, protocols, and clinical research to fulfill job responsibilities.
- Gain practical experience in study procedures by collaborating with seasoned clinical professionals.
- Under close supervision, execute site selection (if applicable), initiation, monitoring, and closure visits in accordance with the contracted scope of work and good clinical practices.
- Provide protocol and related study training to assigned sites, establishing consistent communication channels to manage ongoing 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.
- Oversee the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution. May support the start-up phase under close supervision.
- Create and maintain accurate documentation regarding site management, monitoring visit findings, and action plans by submitting regular visit reports and generating follow-up correspondence.
- Collaborate with study team members to provide project execution support as needed.
Qualifications:
- Bachelor's degree, preferably in healthcare or a related scientific field.
- Proficient written and verbal communication skills in English.
- Computer literacy, including proficiency in Microsoft Word, Excel, PowerPoint, and Outlook.
- Strong organizational and problem-solving abilities.
- Effective time management skills.
This internship presents an excellent opportunity to contribute to impactful projects within the life sciences sector while developing essential skills in clinical research.
About IQVIA: IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services tailored for the life sciences industry. We are committed to pushing the boundaries of human science and data science to create significant impacts, helping our clients foster a healthier world.
