Clinical Research Coordinator
4 weeks ago
We are seeking a highly skilled Clinical Research Administrator to oversee and coordinate clinical trials, ensuring compliance with regulations and collecting and analyzing critical data.
- Coordinate all activities for setting up and monitoring a study, completing accurate study status reports, and maintaining study documentation.
- Run sponsor-generated queries efficiently and take responsibility for study cost efficiency, participating in the preparation and review of study documentation and feasibility studies for new proposals as required.
- Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
- Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.
- University degree in medicine, science, or equivalent.
- Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data.
- Excellent written and verbal communication in English.
- Good social skills enabling you to deal with queries in a timely manner.
- Ability to travel at least 60% of the time (international and domestic - fly and drive) and possess a valid driver's license.
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Clinical Research Coordinator
2 weeks ago
Reading, Reading, United Kingdom Pharmiweb Full timeClinical Trial AssistantWe are seeking a highly organized and detail-oriented Clinical Trial Assistant to join our team at IQVIA UK. As a Clinical Trial Assistant, you will play a critical role in ensuring the successful execution of clinical trials.Key Responsibilities:Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with...
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Clinical Research Coordinator
2 weeks ago
Reading, Reading, United Kingdom Pharmiweb Full timeClinical Trial AssistantWe are seeking a highly organized and detail-oriented Clinical Trial Assistant to join our team at IQVIA UK. As a Clinical Trial Assistant, you will play a critical role in ensuring the successful execution of clinical trials.Key Responsibilities:Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with...
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Clinical Research Coordinator
2 weeks ago
Reading, Reading, United Kingdom Lifelancer Full timeJob Title: Clinical Trial AssistantWe are seeking a highly organized and detail-oriented Clinical Trial Assistant to join our team at Lifelancer, a talent-hiring platform in Life Sciences, Pharma, and IT.Key Responsibilities:Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...
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Clinical Research Coordinator
2 weeks ago
Reading, Reading, United Kingdom Lifelancer Full timeJob Title: Clinical Trial AssistantWe are seeking a highly organized and detail-oriented Clinical Trial Assistant to join our team at Lifelancer, a talent-hiring platform in Life Sciences, Pharma, and IT.Key Responsibilities:Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...
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Clinical Research Coordinator
2 months ago
Reading, Reading, United Kingdom ICON Plc Full timeJob Summary:ICON Plc is seeking a highly skilled Clinical Research Associate to join our dynamic team. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.Key Responsibilities:Coordinate all activities for setting...
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Clinical Research Coordinator
2 months ago
Reading, Reading, United Kingdom ICON Plc Full timeJob Summary:ICON Plc is seeking a highly skilled Clinical Research Associate to join our dynamic team. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.Key Responsibilities:Coordinate all activities for setting...
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Clinical Research Coordinator
2 weeks ago
Reading, Reading, United Kingdom Pharmiweb Full timeJob OverviewWe are seeking a highly organized and detail-oriented Clinical Trials Assistant to join our team. As a Clinical Trials Assistant, you will play a critical role in ensuring the successful execution of clinical trials by providing administrative support to our Clinical Research Associates and Regulatory and Start-Up teams.Key ResponsibilitiesAssist...
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Clinical Research Coordinator
2 weeks ago
Reading, Reading, United Kingdom Pharmiweb Full timeJob OverviewWe are seeking a highly organized and detail-oriented Clinical Trials Assistant to join our team. As a Clinical Trials Assistant, you will play a critical role in ensuring the successful execution of clinical trials by providing administrative support to our Clinical Research Associates and Regulatory and Start-Up teams.Key ResponsibilitiesAssist...
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Clinical Research Coordinator
18 minutes ago
Reading, Reading, United Kingdom Pharmiweb Full timeJob Overview:As a Clinical Trials Assistant, you will play a vital role in ensuring the successful execution of clinical trials. You will be responsible for providing administrative support to the clinical team, ensuring that all clinical documents and systems are accurately updated and maintained. This position requires strong organizational skills and...
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Clinical Research Associate
1 month ago
Reading, Reading, United Kingdom IQVIA Argentina Full timeJob Title: Clinical Research AssociateAt IQVIA, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in ensuring the success of our clinical trials by providing administrative support to our Clinical Research Associates and Regulatory and Start-Up teams.Key...
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Clinical Research Associate
1 month ago
Reading, Reading, United Kingdom IQVIA Argentina Full timeJob Title: Clinical Research AssociateAt IQVIA, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in ensuring the success of our clinical trials by providing administrative support to our Clinical Research Associates and Regulatory and Start-Up teams.Key...
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Clinical Research Coordinator
1 week ago
Reading, Reading, United Kingdom Pharmiweb Full timeJob OverviewAs a Clinical Trials Assistant, you will play a crucial role in ensuring the smooth execution of clinical trials. Your primary responsibility will be to provide administrative support to the Clinical Research Associates and Regulatory and Start-Up teams.Key ResponsibilitiesAssist in maintaining clinical documents and systems, including the Trial...
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Clinical Research Coordinator
1 week ago
Reading, Reading, United Kingdom Pharmiweb Full timeJob OverviewAs a Clinical Trials Assistant, you will play a crucial role in ensuring the smooth execution of clinical trials. Your primary responsibility will be to provide administrative support to the Clinical Research Associates and Regulatory and Start-Up teams.Key ResponsibilitiesAssist in maintaining clinical documents and systems, including the Trial...
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Clinical Research Associate
1 week ago
Reading, Reading, United Kingdom IQVIA Argentina Full timeAt IQVIA, we are seeking a highly skilled Clinical Research Associate to join our team. As a key member of our Clinical Research team, you will play a critical role in ensuring the successful delivery of clinical trials.Key Responsibilities:Assist Clinical Research Associates and Regulatory and Start-Up teams with updating and maintaining clinical documents...
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Clinical Research Associate
2 weeks ago
Reading, Reading, United Kingdom IQVIA Argentina Full timeJob Title: Clinical Research AssociateAt IQVIA, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in ensuring the success of our clinical trials by providing administrative support to our Clinical Research Associates and Regulatory and Start-Up teams.Key...
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Clinical Research Associate
2 weeks ago
Reading, Reading, United Kingdom IQVIA Argentina Full timeJob Title: Clinical Research AssociateAt IQVIA, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in ensuring the success of our clinical trials by providing administrative support to our Clinical Research Associates and Regulatory and Start-Up teams.Key...
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Clinical Research Associate
1 month ago
Reading, Reading, United Kingdom IQVIA Argentina Full timeJob Title: Clinical Research AssociateAt IQVIA, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in ensuring the success of our clinical trials by providing administrative support to our Clinical Research Associates and Regulatory and Start-Up teams.Key...
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Clinical Research Associate
1 month ago
Reading, Reading, United Kingdom IQVIA Argentina Full timeJob Title: Clinical Research AssociateAt IQVIA, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in ensuring the success of our clinical trials by providing administrative support to our Clinical Research Associates and Regulatory and Start-Up teams.Key...
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Clinical Research Associate
4 weeks ago
Reading, Reading, United Kingdom Lifelancer Full timeSeeking a Clinical Research AssociateWe are currently seeking a highly skilled Clinical Research Associate to join our team at Lifelancer. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.Key...
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Clinical Research Associate
4 weeks ago
Reading, Reading, United Kingdom Lifelancer Full timeSeeking a Clinical Research AssociateWe are currently seeking a highly skilled Clinical Research Associate to join our team at Lifelancer. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.Key...