Clinical Trials Site Acquisition Specialist

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...

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...

Job DescriptionWe are searching for a highly skilled Clinical Trials Operations Specialist to join our team at PSI CRO.About the RoleThis is an exciting opportunity to work in a dynamic environment where you will be responsible for identifying and recruiting clinical trial sites. You will be working closely with cross-functional teams to drive project...

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...

Clinical Site Ambassador Role at Advanced ClinicalThe Clinical Site Ambassador will be responsible for developing and maintaining relationships with clinical sites throughout Italy, working closely with the client to ensure effective site management and monitoring.This role requires a strong understanding of site capabilities and structure, as well as...

Job DescriptionAs a key member of our team, you will be responsible for supporting the conduct and patient recruitment of global clinical trials at investigative sites. This role requires strong expertise in site engagement and clinical trial monitoring.ResponsibilitiesParticipate in study-level feasibility activities, providing valuable insights on...

Job DescriptionThe Clinical Site Liaison is a field-based expert who supports the conduct and patient recruitment of global clinical trials at investigative sites. This role requires a deep understanding of patient pathways and trial recruitment, as well as excellent communication and presentation skills.Key Responsibilities:Participate in feasibility...

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...

Key Responsibilities:As a Clinical Trial Physician, Phase I, you will provide medical leadership to study teams, ensuring the delivery of high-quality study data within time and budget. Your expertise will be crucial in creating clinical trial protocols, contributing to site selection, and reviewing study protocols and amendments.Key Skills: Strong clinical...

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...

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,...

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...

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 SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at Allucent. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials at investigator sites, ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements.Key Responsibilities:Conduct site initiation,...

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 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 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 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...