Senior Clinical Research Associate I

Job SummaryWe are seeking a highly skilled Senior Clinical Research Associate to join our team at Pharmiweb. As a Senior Clinical Research Associate, you will be responsible for site monitoring and site management, ensuring the implementation of project plans and assuming line management responsibilities as assigned.Key ResponsibilitiesResponsible for all...

Job SummaryAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Pharmiweb provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.With over...

We are seeking a Clinical Associate to support the planning, execution, and monitoring of clinical trials. The successful candidate will assist in ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.The Clinical Associate will coordinate study activities, including site initiation, patient recruitment, data collection,...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at Pharmiweb. As a key member of our clinical operations team, you will be responsible for ensuring the smooth conduct of clinical trials, from site qualification to close-out visits.Your primary focus will be on performing site qualification, site initiation, interim...

About the RoleParexel is a leading provider of biopharmaceutical services, dedicated to improving global health by transforming scientific discoveries into new treatments.We are seeking a highly skilled Clinical Research Associate II to join our Clinical Operations Team in Spain, with the opportunity to work in an office-based setting in Madrid or...

Job Summary We are seeking a Clinical Associate to support the design, implementation, and management of clinical trials. This role will involve assisting in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.Key ResponsibilitiesAssist in the planning,...

Job SummaryAs a Clinical Research Associate at Pharmiweb, you will play a critical role in ensuring the success of our clinical trials. Your primary responsibility will be to perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits, ensuring regulatory, ICH-GCP, and protocol compliance.Key...

Study Start Up Associate II RoleAt ICON, we're seeking a highly skilled Study Start Up Associate II to join our dynamic team. As a Study Start Up Associate II, you'll play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and...

Clinical Research Associate ISyneos Health is a leading biopharmaceutical solutions organization that accelerates customer success by translating clinical, medical affairs, and commercial insights into outcomes. We have a Clinical Development model that puts the customer and patient at the center of everything we do.We are continuously looking for ways to...

Job SummaryWe are seeking a highly skilled Clinical Research Associate II - Site Management Associate II to join our team at Pharmiweb. This role will be responsible for performing site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.Key...

Job Summary:We are seeking a highly skilled Clinical Research Associate II to join our team at Pharmiweb. As a CRA II, you will be responsible for performing site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.Key Responsibilities:Perform site...

Job Description:Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.Responsibilities:Performs site qualification, site initiation, interim monitoring, site management...

Study Start-up Associate II RoleAt ICON, we seek a highly skilled Study Start-up Associate II to join our team. This role will be pivotal in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.Key Responsibilities:Leading the preparation and...

Job SummaryWe are seeking a highly skilled Senior Clinical Writer to join our team at Pharmiweb. As a key member of our Medical Writing Team, you will be responsible for developing high-quality clinical documents for regulatory submissions globally.Key ResponsibilitiesDevelop scientifically valid, complete, and consistent clinical documents, including...

Study Start Up Associate II Job DescriptionPharmiweb is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence.We're seeking a Study Start Up Associate II to join our diverse and dynamic team. As a Study Start Up Associate II at Pharmiweb, you will play a...

Job SummaryWe are seeking a highly skilled Global Clinical Research Operations Specialist to join our team. As a key member of our clinical operations team, you will be responsible for providing support to the clinical trial team at the global level, impacting directly the project's success.Key ResponsibilitiesKeeping up to date with all the changes/required...

Key Responsibilities:As a Clinical Operations Specialist at Pharmiweb, you will be part of a global clinical research organization that is powered by healthcare intelligence. Your primary role will be to provide support to the clinical trial team, impacting project success directly.Key Tasks:Stay up-to-date with ICH GCP, sponsor's written standards, and...

Job SummaryThe Principal Medical Writer will be responsible for the development of clinical documents for submissions to regulatory authorities globally.As a key member of the IAI Medical Writing Team, you will work directly with multidisciplinary project team members to write scientifically valid, complete, and consistent documents such as clinical study...

Job Summary:We are seeking a highly skilled Senior Medical Writer to join our team at Syneos Health. As a key member of our medical writing team, you will be responsible for developing high-quality clinical documents, including protocols, reports, and submissions, while collaborating with cross-functional teams to ensure timely and accurate delivery of...

Job SummaryWe are seeking a highly skilled Senior Biostatistician to join our team at Syneos Health. As a key member of our biostatistics department, you will be responsible for providing statistical expertise and guidance to support the development of clinical trials.Key Responsibilities:Provide statistical support and guidance to biostatisticians on...