Clinical Trials Operations Specialist

Job SummaryWe are seeking a highly skilled Site Identification Specialist to join our team at PSI CRO. As a Site Identification Specialist, you will be responsible for identifying and evaluating potential clinical trial sites, collaborating with medical professionals, and ensuring comprehensive internal handovers.Key ResponsibilitiesInvolved with in-house...

Job Title: Senior Clinical Operations SpecialistAt ICON, we're dedicated to delivering innovative healthcare solutions that drive excellence in clinical research. We're seeking an experienced Senior Clinical Operations Specialist to join our team in Italy.Key Responsibilities:Assess and qualify potential investigative sites for clinical trials.Monitor and...

Job DescriptionAs a Clinical Trials Placement Specialist at Psi Cro, you will be involved in setting clinical trials related collaboration with medical professionals. Your responsibilities will include defining the optimal site profile for a study, recommending high-quality sites, and creating a site identification tracker. You will also communicate with...

Senior Clinical Trials Manager - Pharmaceuticals - EU LocationsWe seek a highly skilled Senior Clinical Trials Manager to join our North Carolina based client, a leading company in the research, development, and commercialization of life-changing products.This is an exciting opportunity to contribute to their portfolio of groundbreaking products as a Senior...

**Job Overview**Cmed Group Ltd is an innovative Contract Research Organization (CRO) with a strong reputation for delivering complex clinical trials. We are seeking an experienced Senior Clinical Trials Manager to lead our team in the operational delivery of clinical trials.**Key Responsibilities:**Plan and execute multiple phase I-IV studies to agreed...

Job Title: Senior Clinical Research Associate - Clinical Trials ExpertAbout the Role:We are seeking an experienced Senior Clinical Research Associate to join our team in Italy. As a Senior Clinical Research Associate, you will be responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies. You will work closely...

At Jefferson Wells, we are seeking a highly skilled QC Clinical GCP Specialist to join our team. This key role is responsible for ensuring that clinical trials are conducted in accordance with current national and international legislation, guidelines, and company standard operating procedures. The Quality Assurance Specialist will be responsible for the...

Clinical Site Liaison Job DescriptionAs a Clinical Site Liaison at Pharmiweb, you will be part of the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence. Your role will be to support the conduct and patient recruitment of global clinical trials at investigative sites through local and relational...

Translation Opportunity at PSIWe are seeking a skilled Clinical Trials Translator to join our team and contribute to the success of our global clinical trials of novel pharmaceuticals.You will:• Translate clinical trial/medical documentation, including business and technical documents• Customize translations to meet regulatory requirements• Edit,...

Quality Assurance in Clinical TrialsJefferson Wells is hiring a Quality Assurance Specialist to support a pharmaceutical company in Milano, Italy.The QA Specialist will ensure that clinical trials are conducted in accordance with current national and international legislation, guidelines, and company standard operating procedures.Key responsibilities...

Job OverviewAllucent is a leading biopharmaceutical company that specializes in helping small-medium companies navigate the complex world of clinical trials. We are seeking an experienced Clinical Research Associate II to join our team and play a crucial role in ensuring the success of our clinical studies.

Job Title: QC Clinical GCP SpecialistJefferson Wells is seeking a QC Clinical GCP Specialist on behalf of a pharmaceutical company based in Lombardia. The successful candidate will ensure that clinical trials are conducted in accordance with current national and international legislation, relevant guidelines, and the company's standard operating...

Job OverviewPsi Ind is a leading global Contract Research Organization (CRO) dedicated to delivering high-quality clinical trials. We are seeking an experienced Clinical Data Manager to join our team in streamlining our clinical data management process.About the RoleThe Clinical Data Manager will play a vital role in managing clinical data activities for...

Job Opportunity:PSI is seeking a highly skilled Translator/Interpreter to join our team and contribute to the success of our global clinical trials of novel pharmaceuticals.You will be responsible for translating clinical trial/medical documentation, business and technical documents, and customizing translations to meet regulatory requirements.Key...

Job Title: SAS Programmer I - Clinical Trials ProfessionalWe are seeking a skilled SAS Programmer I to contribute to our global clinical trials team. As a SAS Programmer I, you will work closely with international teams of statisticians, programmers, and data managers to develop analysis data sets, program data sets and summaries, and support SAS program...

Job OpportunityPSI is seeking a skilled Senior Clinical Trials Translator to join our team. As a key member of our global translation services, you will play a crucial role in providing high-quality translations for clinical trials of novel pharmaceuticals.You will: Translate clinical trial/medical documentation, business, and technical documents Customize...

Job Title: Clinical QA SpecialistJefferson Wells is seeking a highly skilled Clinical QA Specialist to support our client, a pharmaceutical company based in Milano (Lombardia).Main Responsibilities:Contribute to the development and updating of Standard Operating Procedures (SOPs) related to clinical trials to ensure compliance with Good Clinical Practice...

Novartis Farmacéutica seeks a skilled Clinical Study Contracting Specialist to support the coordination, preparation, and execution of clinical study contracts. The ideal candidate will have a strong background in contract management and a solid understanding of clinical trials.Main Responsibilities:Coordinate the preparation and execution of clinical study...

Job DescriptionJefferson Wells is seeking a highly skilled Clinical QA Specialist to support the quality assurance of clinical trials. The successful candidate will ensure compliance with national and international regulations, guidelines, and company standard operating procedures.Main Responsibilities:Contribute to the development and updating of Standard...

About the RoleWe are seeking a highly skilled Medical Director to provide medical support and advice for clinical trials and safety evaluation within our Pharmacovigilance department.Key ResponsibilitiesProvide medical leadership to study teams, including creating clinical trial protocols and implementing the latest scientific information.Conduct real-time...