Clinical Research Associate II
1 settimana fa
We are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for ensuring the successful execution of clinical trials.
Key Responsibilities:- Monitor and control investigation sites to ensure compliance with study protocols and regulatory requirements.
- Perform site initiation, monitoring, and closure visits to ensure data quality and integrity.
- Track and supervise the collection of study data to ensure timely and accurate reporting.
- Review and collect regulatory documents as required.
- Prepare and submit site visit reports and telephone contact reports.
- Maintain and update the Clinical Trial Management System (CTMS) to ensure accurate and up-to-date information.
- Act as the primary point of contact for site staff and ensure effective communication with the project team.
- Collaborate with the Centralized Monitoring Team to evaluate risk-based monitoring activities and ensure the quality of study conduct.
- Identify and resolve site issues, including recruitment challenges and logistical problems.
- Ensure the continuous maintenance of the Trial Master File and Investigator Site File.
- Assist the Project Manager and Clinical Team Leader with the generation of study-specific forms and follow-up with the teams to ensure timely completion and submission.
- At least 2 years of experience in clinical research.
- Strong therapeutic background and knowledge of clinical trials.
- Ability to travel for up to 8 days per month, depending on project needs.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Strong organizational and problem-solving skills.
- Ability to define and meet project requirements.
- Flexibility and adaptability in a fast-paced environment.
- Comprehensive benefits package.
- Competitive salary.
- Departmental study/training budget for professional development.
- Flexible working hours.
- Opportunity for remote/hybrid working.
- Leadership and mentoring opportunities.
- Participation in our Buddy Program.
- Internal growth opportunities and career progression.
- Financially rewarding internal employee referral program.
- Access to online soft-skills and technical training.
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Clinical Research Associate II
4 settimane fa
Milano, Lombardia, Italia Psi Cro Ag A tempo pieno{"title": "Clinical Research Associate II", "subtitle": "Join our team of experts in clinical research", "content": "At PSI Cro Ag, we are seeking a highly skilled Clinical Research Associate II to join our team. As a Clinical Research Associate II, you will be responsible for conducting and reporting onsite monitoring visits, performing CRF review, source...
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Clinical Research Associate II
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Milano, Lombardia, Italia Psi Cro Ag A tempo pienoJoin Our Team as a Clinical Research Associate IIAt PSI Cro Ag, we are seeking a highly skilled Clinical Research Associate II to join our team. As a key member of our clinical research team, you will be responsible for conducting and reporting onsite monitoring visits, performing CRF review, and ensuring the highest quality standards in the industry.Key...
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Clinical Research Associate II
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Milano, Lombardia, Italia Psi Cro Ag A tempo pienoJoin Our Team as a Clinical Research Associate IIAt PSI Cro Ag, we are seeking a highly skilled Clinical Research Associate II to join our team. As a key member of our clinical research team, you will be responsible for conducting and reporting onsite monitoring visits, performing CRF review, source document verification, and query resolution.Key...
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Clinical Research Associate II
3 settimane fa
Milano, Lombardia, Italia Allucent A tempo pienoJob Title: Clinical Research Associate IIWe are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for ensuring the successful execution of clinical trials.Key Responsibilities:Monitor and control investigation sites to ensure compliance with study...
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Clinical Research Associate II
4 settimane fa
Milano, Lombardia, Italia Allucent A tempo pienoJob Title: Clinical Research Associate IIWe are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for ensuring the successful execution of clinical trials.Key Responsibilities:Monitor and control investigation sites to ensure compliance with study...
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Milano, Lombardia, Italia Allucent A tempo pienoJob Title: Clinical Research Associate IIWe are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for ensuring the successful execution of clinical trials.Key Responsibilities:Monitor and control investigation sites to ensure compliance with study...
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Clinical Research Associate II
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Milano, Lombardia, Italia Allucent A tempo pienoJob Title: Clinical Research Associate IIWe are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for ensuring the successful execution of clinical trials.Key Responsibilities:Monitor and control investigation sites to ensure compliance with trial...
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Clinical Research Associate II
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Milano, Lombardia, Italia Allucent A tempo pienoJob Title: Clinical Research Associate IIWe are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a Clinical Research Associate II, you will play a critical role in ensuring the success of our clinical trials by monitoring and managing investigation sites, detecting and resolving issues, and ensuring compliance with...
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Clinical Research Associate II
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Milano, Lombardia, Italia Allucent A tempo pienoAbout the RoleWe are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a Clinical Research Associate II, you will play a critical role in the success of our clinical trials by ensuring that investigation sites are monitored and managed in accordance with the trial protocol and regulatory requirements.Key...
