Aktualne oferty pracy związane z Adverse Event Coordinator with Proficiency in Clinical Trials - Warszawa, Mazovia - IQVIA
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Global Clinical Trials Coordinator
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Warszawa, Mazovia, Polska PSI CRO Pełny etatClinical Trials Business Development RepresentativeFull-timeMilestone One is a Site Enabling Organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery.The Milestone One Business Development Representative role supports a Business Development...
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Adverse Event Intake Specialist with English language
2 tygodni temu
Warszawa, Mazovia, Polska IQVIA Pełny etatIQVIA Adverse Event Intake Specialist with English language in Warsaw, PolandApply your knowledge and expertise, including complex decision making, to review, assess and process safety and product quality information. Be a part of a global team to help ensure the safety profiles of products marketed around the world with development opportunities to...
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Clinical Trials Writer
6 dni temu
Warszawa, Mazovia, Polska GlaxoSmithKline Pełny etatAbout the OpportunityWe are seeking an accomplished Clinical Trials Writer to join our team at GlaxoSmithKline. This role involves developing clinical trial documents and managing projects to ensure timely delivery of high-quality documents.Key Responsibilities:Clinical Trial Document Development: Develop and review clinical trial documents, including...
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Warszawa, Mazovia, Polska Milestone One Pełny etatClinical Trials Business Development Representative2 days ago Be among the first 25 applicantsMilestone One is a Site Enabling Organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery.Job DescriptionThe Milestone One Business Development...
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Site Coordinator
2 tygodni temu
Warszawa, Mazovia, Polska TN Poland Pełny etatSocial network you want to login/join with:ResponsibilitiesActs as the main line of communication between the Sponsor or CRO and the medical institution.Builds and maintains good rapport with the medical staff and with Sponsor or CRO representatives involved in clinical trials.Facilitates the evaluation of proposed studies and ensures responses to...
Adverse Event Coordinator with Proficiency in Clinical Trials
2 tygodni temu
We are seeking a highly organized Adverse Event Coordinator to join our team. As an Adverse Event Coordinator, you will be responsible for coordinating and managing adverse event reports and ensuring compliance with regulatory requirements.
About the Role
In this role, you will work closely with senior operation team members to coordinate and manage adverse event reports. You will also collaborate with cross-functional teams to ensure compliance with regulatory requirements.
Main Responsibilities
- Coordinate and manage adverse event reports
- Ensure compliance with regulatory requirements
- Collaborate with cross-functional teams to achieve business objectives
- Maintain accurate records of all adverse event reports
- Develop and implement procedures to ensure compliance with regulatory requirements
Skills and Qualifications
- Bachelor's Degree in Life Science or healthcare-related discipline is required
- Minimum 2 years of experience in pharmacovigilance or related field
- Excellent written and verbal skills in English (min. C1)
- Ability to work effectively on multiple projects simultaneously, organize own workload, and effectively manage competing priorities
